Variant report

Variant	rs6560645
Chromosome Location	chr9:139621826-139621827
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:82)
CpG islands
(count:0)
Chromatin interactive
region (count:72)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:82 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr9:139621708-139623134	GM12892	blood:	n/a	n/a
2	POLR2A	chr9:139619685-139623692	GM12892	blood:	n/a	n/a
3	POLR2A	chr9:139621663-139622975	HUVEC	blood vessel:	n/a	n/a
4	ESRRA	chr9:139621669-139623501	GM12878	blood:	n/a	chr9:139623204-139623217
5	POLR2A	chr9:139613661-139625070	K562	blood:	n/a	n/a
6	REST	chr9:139621800-139622362	A549	lung:	n/a	chr9:139622051-139622061
7	BCL3	chr9:139620898-139622243	A549	lung:	n/a	n/a
8	SIN3AK20	chr9:139619836-139623651	MCF-7	breast:	n/a	n/a
9	POLR2A	chr9:139615152-139624044	PFSK-1	brain:	n/a	n/a
10	POLR2A	chr9:139621703-139623023	ECC-1	luminal epithelium:	n/a	n/a
11	POLR2A	chr9:139614438-139623107	H1-hESC	embryonic stem cell:	n/a	n/a
12	POLR2A	chr9:139621029-139623177	GM12878	blood:	n/a	n/a
13	CTCF	chr9:139621740-139621890	AoAF	blood vessel:	n/a	n/a
14	CHD1	chr9:139621269-139622925	H1-hESC	embryonic stem cell:	n/a	chr9:139622127-139622137 chr9:139622655-139622662 chr9:139622740-139622750
15	POLR2A	chr9:139621800-139622994	Hela-S3	cervix:	n/a	n/a
16	SP1	chr9:139621779-139622970	A549	lung:	n/a	chr9:139622697-139622706 chr9:139622697-139622707
17	POLR2A	chr9:139615050-139622967	PFSK-1	brain:	n/a	n/a
18	POLR2A	chr9:139621672-139622983	K562	blood:	n/a	n/a
19	POLR2A	chr9:139619861-139623901	K562	blood:	n/a	n/a
20	MAX	chr9:139621819-139623947	A549	lung:	n/a	chr9:139622751-139622760 chr9:139622753-139622762 chr9:139622752-139622759 chr9:139622751-139622761
21	POLR2A	chr9:139619842-139623939	HL-60	blood:	n/a	n/a
22	CTCF	chr9:139621700-139621850	GM12864	blood:	n/a	n/a
23	POLR2A	chr9:139619918-139622987	GM12878	blood:	n/a	n/a
24	POLR2A	chr9:139619189-139625931	HepG2	liver:	n/a	n/a
25	POLR2A	chr9:139619715-139623033	U87	brain:	n/a	n/a
26	POLR2A	chr9:139619810-139623525	K562	blood:	n/a	n/a
27	MAX	chr9:139621825-139623604	MCF-7	breast:	n/a	chr9:139622751-139622760 chr9:139622753-139622762 chr9:139622752-139622759 chr9:139622751-139622761
28	POLR2A	chr9:139621723-139622994	HCT-116	colon:	n/a	n/a
29	POLR2A	chr9:139619759-139623003	GM12891	blood:	n/a	n/a
30	POLR2A	chr9:139614441-139624589	SK-N-MC	brain:	n/a	n/a
31	CTCF	chr9:139621740-139621890	GM12872	blood:	n/a	n/a
32	POLR2A	chr9:139620876-139624117	MCF10A-Er-Src	breast:	n/a	n/a
33	MAX	chr9:139620254-139624067	A549	lung:	n/a	chr9:139622751-139622760 chr9:139622753-139622762 chr9:139622752-139622759 chr9:139622751-139622761
34	POLR2A	chr9:139621703-139622879	GM12891	blood:	n/a	n/a
35	POLR2A	chr9:139611785-139624497	K562	blood:	n/a	n/a
36	POLR2A	chr9:139614461-139623997	HUVEC	blood vessel:	n/a	n/a
37	HCFC1	chr9:139620113-139623383	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr9:139619954-139623122	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr9:139621768-139622806	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr9:139619722-139623801	HUVEC	blood vessel:	n/a	n/a
41	POLR2A	chr9:139620749-139624121	MCF10A-Er-Src	breast:	n/a	n/a
42	HEY1	chr9:139619111-139623430	K562	blood:	n/a	chr9:139622860-139622875 chr9:139622697-139622712 chr9:139623025-139623040 chr9:139622886-139622901
43	POLR2A	chr9:139619788-139622935	GM12878	blood:	n/a	n/a
44	HEY1	chr9:139621661-139623362	K562	blood:	n/a	chr9:139622860-139622875 chr9:139622697-139622712 chr9:139623025-139623040 chr9:139622886-139622901
45	POU2F2	chr9:139621640-139622195	GM12891	blood:	n/a	n/a
46	POLR2A	chr9:139614456-139622946	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr9:139621761-139623119	GM12878	blood:	n/a	n/a
48	KAP1	chr9:139620896-139623068	HEK293	kidney:	n/a	n/a
49	POLR2A	chr9:139615036-139623045	GM12878	blood:	n/a	n/a
50	POLR2A	chr9:139621698-139621888	A549	lung:	n/a	n/a

No data

(count:72 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:139570497..139595051-chr9:139610806..139626266,85	MCF-7	breast:
2	chr9:139564974..139568395-chr9:139620785..139624804,6	MCF-7	breast:
3	chr9:139621081..139623716-chr9:139698573..139702303,4	K562	blood:
4	chr9:139621097..139622656-chr9:140082279..140085115,2	K562	blood:
5	chr9:139331653..139334460-chr9:139620193..139622356,2	MCF-7	breast:
6	chr8:129060381..129061326-chr9:139621691..139622632,2	NB4	blood:
7	chr9:139621216..139622875-chr9:139685230..139687360,2	MCF-7	breast:
8	chr9:139621145..139622872-chr9:139718772..139721878,3	K562	blood:
9	chr9:139559252..139566873-chr9:139615343..139623790,23	MCF-7	breast:
10	chr9:139619516..139623685-chr9:139693810..139697808,6	K562	blood:
11	chr9:139620315..139626197-chr9:139646581..139660029,24	MCF-7	breast:
12	chr9:139620423..139623520-chr9:139779258..139782010,3	K562	blood:
13	chr9:139616966..139626046-chr9:139651480..139662091,27	MCF-7	breast:
14	chr9:139376700..139379516-chr9:139619052..139623345,7	K562	blood:
15	chr9:139621206..139624482-chr9:139640401..139643595,4	MCF-7	breast:
16	chr9:139619516..139624583-chr9:139694122..139697808,6	K562	blood:
17	chr9:139621166..139623955-chr9:139702630..139705456,7	K562	blood:
18	chr9:139621075..139623829-chr9:139838145..139840956,4	K562	blood:
19	chr9:139621283..139623624-chr9:139709287..139711634,2	K562	blood:
20	chr9:139621177..139623935-chr9:139715647..139719817,3	MCF-7	breast:
21	chr9:139620963..139623863-chr9:139946422..139948967,2	K562	blood:
22	chr7:84568918..84570842-chr9:139619990..139622918,5	MCF-7	breast:
23	chr9:139586216..139592582-chr9:139618001..139626030,23	MCF-7	breast:
24	chr9:139621166..139623785-chr9:139780041..139782196,3	K562	blood:
25	chr9:139440519..139442759-chr9:139620071..139622669,2	MCF-7	breast:
26	chr9:139376314..139380925-chr9:139621169..139625507,6	MCF-7	breast:
27	chr9:139621146..139622893-chr9:139980116..139982904,2	K562	blood:
28	chr9:139621264..139624234-chr9:139940317..139942118,2	K562	blood:
29	chr9:139376144..139379676-chr9:139621146..139625438,7	K562	blood:
30	chr9:139619929..139623671-chr9:139747589..139752463,5	K562	blood:
31	chr9:139618685..139627120-chr9:139649384..139659403,28	K562	blood:
32	chr9:139550367..139553990-chr9:139620470..139623821,3	MCF-7	breast:
33	chr9:139496776..139498565-chr9:139620965..139623947,2	K562	blood:
34	chr9:139621035..139624561-chr9:139681529..139687287,9	K562	blood:
35	chr9:139621304..139624184-chr9:139872879..139875710,3	K562	blood:
36	chr9:139620788..139624093-chr9:139694172..139695988,3	MCF-7	breast:
37	chr9:139619134..139621860-chr9:140316424..140318668,2	MCF-7	breast:
38	chr9:139620118..139623932-chr9:139922375..139925511,3	MCF-7	breast:
39	chr9:139620633..139624484-chr9:139701088..139704302,3	MCF-7	breast:
40	chr9:139621304..139623071-chr9:139872879..139875710,2	K562	blood:
41	chr9:139620467..139623691-chr9:139756256..139761738,5	K562	blood:
42	chr9:139619899..139624270-chr9:139920948..139923440,3	MCF-7	breast:
43	chr9:139620752..139623162-chr9:139701207..139703819,3	MCF-7	breast:
44	chr9:139610819..139629219-chr9:139630372..139645615,53	MCF-7	breast:
45	chr9:139621595..139623211-chr9:139759384..139761536,2	MCF-7	breast:
46	chr9:139621278..139624827-chr9:139660350..139665047,5	K562	blood:
47	chr9:139440721..139444129-chr9:139620823..139623171,3	K562	blood:
48	chr9:139255640..139259795-chr9:139620500..139624170,6	K562	blood:
49	chr9:139257144..139260573-chr9:139620692..139623633,4	K562	blood:
50	chr7:84567429..84570853-chr9:139619029..139623910,14	K562	blood:

No data

Variant related genes	Relation type
SNHG7	TF binding region
ENSG00000172889	Chromatin interaction
ENSG00000107281	Chromatin interaction
ENSG00000155090	Chromatin interaction
ENSG00000204003	Chromatin interaction
ENSG00000169583	Chromatin interaction
ENSG00000237886	Chromatin interaction
ENSG00000177984	Chromatin interaction
ENSG00000228544	Chromatin interaction
ENSG00000267206	Chromatin interaction
ENSG00000272896	Chromatin interaction
ENSG00000107317	Chromatin interaction
ENSG00000159069	Chromatin interaction
ENSG00000265181	Chromatin interaction
ENSG00000272679	Chromatin interaction
ENSG00000232019	Chromatin interaction
ENSG00000213221	Chromatin interaction
ENSG00000148384	Chromatin interaction
ENSG00000127191	Chromatin interaction
ENSG00000273066	Chromatin interaction
ENSG00000266507	Chromatin interaction
ENSG00000199161	Chromatin interaction
ENSG00000184709	Chromatin interaction
ENSG00000185863	Chromatin interaction
ENSG00000261793	Chromatin interaction
ENSG00000054179	Chromatin interaction
ENSG00000204001	Chromatin interaction
ENSG00000176919	Chromatin interaction
ENSG00000252440	Chromatin interaction
ENSG00000054148	Chromatin interaction
ENSG00000213212	Chromatin interaction
ENSG00000196366	Chromatin interaction
ENSG00000176248	Chromatin interaction
ENSG00000107223	Chromatin interaction
ENSG00000187922	Chromatin interaction
ENSG00000188747	Chromatin interaction
ENSG00000177943	Chromatin interaction
ENSG00000169692	Chromatin interaction
ENSG00000244187	Chromatin interaction
ENSG00000139437	Chromatin interaction
ENSG00000196642	Chromatin interaction
ENSG00000177239	Chromatin interaction
ENSG00000268996	Chromatin interaction
ENSG00000236394	Chromatin interaction
ENSG00000263697	Chromatin interaction
ENSG00000221693	Chromatin interaction
ENSG00000107331	Chromatin interaction
ENSG00000148400	Chromatin interaction
ENSG00000187609	Chromatin interaction
ENSG00000213213	Chromatin interaction
ENSG00000180539	Chromatin interaction
ENSG00000176101	Chromatin interaction

Extended variants
information (count: 83 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10781513	0.96[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10870115	0.97[AFR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11793962	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11849	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2275161	0.97[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3739939	0.80[EUR][1000 genomes]
rs55807337	0.82[ASN][1000 genomes]
rs62582194	0.81[ASN][1000 genomes]
rs6560643	0.85[ASN][1000 genomes]
rs6866	0.87[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6873	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7029239	0.82[ASN][1000 genomes]
rs7038042	0.82[ASN][1000 genomes]
rs72761013	0.85[ASN][1000 genomes]
rs73668366	0.81[ASN][1000 genomes]
rs7466679	0.81[ASN][1000 genomes]
rs945381	0.85[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs945383	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:65 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1849811	chr9:138939662-139755001	Bivalent Enhancer Strong transcription Weak transcription Genic enhancers Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	323 gene(s)	inside rSNPs	diseases
2	esv1822553	chr9:138967205-139755539	Genic enhancers Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	323 gene(s)	inside rSNPs	diseases
3	nsv894326	chr9:139057463-139647074	Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	260 gene(s)	inside rSNPs	diseases
4	nsv894337	chr9:139069713-139669111	Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	261 gene(s)	inside rSNPs	diseases
5	esv1851120	chr9:139101947-139711758	Bivalent Enhancer Weak transcription Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	275 gene(s)	inside rSNPs	diseases
6	nsv430118	chr9:139101947-139795504	Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	299 gene(s)	inside rSNPs	diseases
7	nsv894351	chr9:139124856-139679387	Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	262 gene(s)	inside rSNPs	diseases
8	nsv540342	chr9:139218422-139973312	Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	317 gene(s)	inside rSNPs	diseases
9	esv2758204	chr9:139252829-139826485	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	270 gene(s)	inside rSNPs	diseases
10	esv2759720	chr9:139252829-139826485	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	270 gene(s)	inside rSNPs	diseases
11	nsv469918	chr9:139254317-140068342	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	341 gene(s)	inside rSNPs	diseases
12	esv1836722	chr9:139301583-139669111	Bivalent Enhancer Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
13	esv1799492	chr9:139341612-139711758	Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	216 gene(s)	inside rSNPs	diseases
14	esv1807611	chr9:139344200-139633839	Enhancers Flanking Active TSS Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	199 gene(s)	inside rSNPs	diseases
15	nsv540346	chr9:139360142-140164011	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	471 gene(s)	inside rSNPs	diseases
16	esv1803718	chr9:139368953-139643023	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	199 gene(s)	inside rSNPs	diseases
17	esv1851291	chr9:139371234-139669111	Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	200 gene(s)	inside rSNPs	diseases
18	nsv894384	chr9:139376426-139622024	Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	173 gene(s)	inside rSNPs	diseases
19	nsv894385	chr9:139376426-139647074	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	199 gene(s)	inside rSNPs	diseases
20	nsv894386	chr9:139376426-139693992	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	208 gene(s)	inside rSNPs	diseases
21	nsv1039149	chr9:139376829-139991102	Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	303 gene(s)	inside rSNPs	diseases
22	esv1820573	chr9:139377938-139643023	Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
23	esv1839109	chr9:139377938-139660589	Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	198 gene(s)	inside rSNPs	diseases
24	esv1829857	chr9:139385438-139760041	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
25	esv1819204	chr9:139388365-139758238	Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
26	esv1803407	chr9:139393591-139643023	Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
27	esv1803979	chr9:139395473-139979276	Genic enhancers Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	267 gene(s)	inside rSNPs	diseases
28	esv1831778	chr9:139395473-139979276	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	267 gene(s)	inside rSNPs	diseases
29	esv1821575	chr9:139395473-140068342	Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	293 gene(s)	inside rSNPs	diseases
30	nsv8579	chr9:139399884-139654708	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
31	nsv894392	chr9:139403102-139669111	Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
32	nsv894402	chr9:139457506-139634495	Weak transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	158 gene(s)	inside rSNPs	diseases
33	esv2422220	chr9:139478587-140244550	Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	454 gene(s)	inside rSNPs	diseases
34	nsv894409	chr9:139483954-139860264	Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	209 gene(s)	inside rSNPs	diseases
35	nsv894420	chr9:139487092-139634495	Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	154 gene(s)	inside rSNPs	diseases
36	esv1846227	chr9:139487092-139643023	Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	154 gene(s)	inside rSNPs	diseases
37	esv1794085	chr9:139487092-139649379	Weak transcription Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	154 gene(s)	inside rSNPs	diseases
38	esv1837438	chr9:139487092-139660589	Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	155 gene(s)	inside rSNPs	diseases
39	nsv894421	chr9:139487092-139669111	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	155 gene(s)	inside rSNPs	diseases
40	nsv894422	chr9:139487092-139776400	Transcr. at gene 5' and 3' Enhancers Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
41	nsv894428	chr9:139496028-139647074	ZNF genes & repeats Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	154 gene(s)	inside rSNPs	diseases
42	nsv894431	chr9:139522101-139642961	Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	150 gene(s)	inside rSNPs	diseases
43	nsv894432	chr9:139522101-139869914	Flanking Bivalent TSS/Enh Strong transcription Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	205 gene(s)	inside rSNPs	diseases
44	nsv894438	chr9:139544437-139622024	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
45	nsv894439	chr9:139544437-139634495	Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	145 gene(s)	inside rSNPs	diseases
46	nsv894440	chr9:139544437-139841512	Active TSS Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	194 gene(s)	inside rSNPs	diseases
47	nsv894441	chr9:139544437-139860264	Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	201 gene(s)	inside rSNPs	diseases
48	nsv894442	chr9:139544437-140462099	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	469 gene(s)	inside rSNPs	diseases
49	nsv540348	chr9:139550414-139687876	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	151 gene(s)	inside rSNPs	diseases
50	nsv894444	chr9:139553723-139627726	Flanking Bivalent TSS/Enh Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:139619400-139622000	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr9:139619800-139622000	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
3	chr9:139620000-139622000	Transcr. at gene 5' and 3'	K562	blood
4	chr9:139620000-139622200	Transcr. at gene 5' and 3'	A549	lung
5	chr9:139620000-139623000	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr9:139620200-139622000	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
7	chr9:139620400-139623400	Active TSS	Pancreatic Islets	Pancreatic Islet
8	chr9:139620600-139622200	Transcr. at gene 5' and 3'	Primary B cells from peripheral blood	blood
9	chr9:139620600-139622200	Transcr. at gene 5' and 3'	Dnd41	blood
10	chr9:139620600-139622400	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
11	chr9:139620600-139623800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr9:139620800-139622200	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
13	chr9:139621000-139622000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
14	chr9:139621000-139622000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
15	chr9:139621000-139622000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
16	chr9:139621000-139622000	Flanking Active TSS	Stomach Mucosa	stomach
17	chr9:139621000-139622200	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
18	chr9:139621000-139622200	Flanking Active TSS	Duodenum Mucosa	Duodenum
19	chr9:139621000-139622400	Flanking Active TSS	Colonic Mucosa	Colon
20	chr9:139621000-139622600	Flanking Active TSS	Primary hematopoietic stem cells	blood
21	chr9:139621200-139622000	Flanking Active TSS	Primary T cells from cord blood	blood
22	chr9:139621200-139622000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
23	chr9:139621200-139622000	Flanking Active TSS	Fetal Lung	lung
24	chr9:139621200-139622000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
25	chr9:139621200-139622200	Flanking Active TSS	Brain Germinal Matrix	brain
26	chr9:139621200-139622200	Flanking Active TSS	Fetal Thymus	thymus
27	chr9:139621200-139622400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
28	chr9:139621200-139622400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
29	chr9:139621200-139622400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr9:139621200-139622400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr9:139621200-139622400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
32	chr9:139621200-139623000	Active TSS	GM12878-XiMat	blood
33	chr9:139621200-139623400	Active TSS	Lung	lung
34	chr9:139621400-139622200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr9:139621400-139622200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr9:139621400-139622200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
37	chr9:139621400-139622200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
38	chr9:139621400-139622200	Flanking Active TSS	Brain Cingulate Gyrus	brain
39	chr9:139621400-139622200	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
40	chr9:139621400-139622200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
41	chr9:139621400-139622200	Flanking Active TSS	Placenta	Placenta
42	chr9:139621400-139622400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
43	chr9:139621400-139622400	Flanking Active TSS	Primary B cells from cord blood	blood
44	chr9:139621400-139622400	Flanking Active TSS	Liver	Liver
45	chr9:139621400-139622400	Active TSS	Right Atrium	heart
46	chr9:139621400-139622400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
47	chr9:139621400-139622800	Active TSS	Pancreas	Pancrea
48	chr9:139621400-139623000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr9:139621400-139623000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr9:139621400-139623000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell

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