Variant report

Variant	nsv904433
Chromosome Location	chr15:79243571-79310288
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1726)
CpG islands
(count:1647)
Chromatin interactive
region (count:94)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1726 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:79286132-79287159	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:79278252-79278589	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:79280578-79281299	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:79299529-79299871	K562	blood:	n/a	n/a
5	ARID3A	chr15:79244305-79244636	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:79260491-79260716	HepG2	liver:	n/a	n/a
7	ARID3A	chr15:79289371-79289670	HepG2	liver:	n/a	n/a
8	ARID3A	chr15:79299472-79299822	HepG2	liver:	n/a	n/a
9	ATF1	chr15:79299484-79299801	K562	blood:	n/a	n/a
10	ATF1	chr15:79296813-79297099	K562	blood:	n/a	n/a
11	ATF1	chr15:79272101-79272388	K562	blood:	n/a	n/a
12	ATF2	chr15:79269441-79269918	GM12878	blood:	n/a	n/a
13	ATF2	chr15:79296649-79297255	GM12878	blood:	n/a	n/a
14	ATF2	chr15:79269323-79270494	GM12878	blood:	n/a	n/a
15	ATF2	chr15:79271940-79272364	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr15:79296546-79297258	GM12878	blood:	n/a	n/a
17	ATF3	chr15:79296798-79297131	K562	blood:	n/a	n/a
18	ATF3	chr15:79296849-79297071	K562	blood:	n/a	n/a
19	ATF3	chr15:79244352-79244507	K562	blood:	n/a	n/a
20	ATF3	chr15:79299501-79299720	K562	blood:	n/a	n/a
21	BACH1	chr15:79271875-79272225	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr15:79269961-79270395	GM12878	blood:	n/a	n/a
23	BATF	chr15:79269554-79269884	GM12878	blood:	n/a	n/a
24	BATF	chr15:79296631-79297227	GM12878	blood:	n/a	chr15:79296942-79296953
25	BATF	chr15:79270053-79270274	GM12878	blood:	n/a	n/a
26	BATF	chr15:79280848-79281262	GM12878	blood:	n/a	n/a
27	BATF	chr15:79296775-79297183	GM12878	blood:	n/a	chr15:79296942-79296953
28	BCL11A	chr15:79296607-79297191	GM12878	blood:	n/a	chr15:79296747-79296756
29	BCL11A	chr15:79269493-79269946	GM12878	blood:	n/a	n/a
30	BCL11A	chr15:79269508-79269845	GM12878	blood:	n/a	n/a
31	BCL11A	chr15:79296722-79297127	GM12878	blood:	n/a	chr15:79296747-79296756
32	BCL3	chr15:79269445-79269952	GM12878	blood:	n/a	n/a
33	BCL3	chr15:79271800-79272483	A549	lung:	n/a	n/a
34	BCLAF1	chr15:79269028-79270502	GM12878	blood:	n/a	n/a
35	BCLAF1	chr15:79296595-79297341	GM12878	blood:	n/a	chr15:79296747-79296756
36	BCLAF1	chr15:79271804-79272508	GM12878	blood:	n/a	n/a
37	BCLAF1	chr15:79269455-79270396	GM12878	blood:	n/a	n/a
38	BCLAF1	chr15:79280814-79281376	GM12878	blood:	n/a	n/a
39	BHLHE40	chr15:79272012-79272399	K562	blood:	n/a	n/a
40	BHLHE40	chr15:79280687-79281376	GM12878	blood:	n/a	n/a
41	BHLHE40	chr15:79299442-79299726	K562	blood:	n/a	n/a
42	BHLHE40	chr15:79296555-79297233	GM12878	blood:	n/a	n/a
43	BHLHE40	chr15:79283647-79283732	K562	blood:	n/a	n/a
44	BHLHE40	chr15:79244391-79244551	K562	blood:	n/a	n/a
45	BHLHE40	chr15:79269011-79270341	GM12878	blood:	n/a	n/a
46	BHLHE40	chr15:79296907-79297002	K562	blood:	n/a	n/a
47	BHLHE40	chr15:79271115-79271295	GM12878	blood:	n/a	n/a
48	BHLHE40	chr15:79285269-79285704	GM12878	blood:	n/a	n/a
49	BHLHE40	chr15:79308913-79309204	GM12878	blood:	n/a	chr15:79309032-79309041 chr15:79309026-79309047 chr15:79309031-79309040 chr15:79309032-79309041
50	BHLHE40	chr15:79284329-79284521	K562	blood:	n/a	n/a

(count:1647 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:79298637-79298687	HRPEpiC	eye:	n/a
2	chr15:79296585-79296635	SK-N-SH	brain:	n/a
3	chr15:79298678-79298728	MCF10A-Er-Src	breast:	n/a
4	chr15:79298691-79298741	Caco-2	colon:	n/a
5	chr15:79296424-79296474	HPAEpiC	pulmonary alveolar:	n/a
6	chr15:79269735-79269785	NT2-D1	testis:	n/a
7	chr15:79282030-79282080	Hepatocyte	liver:	n/a
8	chr15:79298234-79298284	BE2_C	brain:	n/a
9	chr15:79298691-79298741	SK-N-MC	brain:	n/a
10	chr15:79298234-79298284	SK-N-SH_RA	brain:	n/a
11	chr15:79296377-79296427	AG09319	gingival:	n/a
12	chr15:79254338-79254388	HUVEC	blood vessel:	n/a
13	chr15:79298651-79298701	ProgFib	skin:	n/a
14	chr15:79296424-79296474	ProgFib	skin:	n/a
15	chr15:79296585-79296635	HCT-116	colon:	n/a
16	chr15:79296446-79296496	BE2_C	brain:	n/a
17	chr15:79298384-79298434	Jurkat	blood:	n/a
18	chr15:79297159-79297209	GM06990	blood:	n/a
19	chr15:79296446-79296496	T-47D	breast:	n/a
20	chr15:79269735-79269785	AG09319	gingival:	n/a
21	chr15:79262857-79262907	AG09319	gingival:	n/a
22	chr15:79298234-79298284	SK-N-MC	brain:	n/a
23	chr15:79252815-79252865	SKMC	muscle:	n/a
24	chr15:79296585-79296635	Hela-S3	cervix:	n/a
25	chr15:79297159-79297209	GM19239	blood:	n/a
26	chr15:79298604-79298654	AG04450	lung:	fetal
27	chr15:79296377-79296427	NH-A	brain:	n/a
28	chr15:79298691-79298741	T-47D	breast:	n/a
29	chr15:79296446-79296496	HNPCEpiC	eye:	n/a
30	chr15:79283460-79283510	HRE	kidney:	n/a
31	chr15:79282030-79282080	AG04450	lung:	fetal
32	chr15:79254454-79254504	GM12891	blood:	n/a
33	chr15:79297159-79297209	T-47D	breast:	n/a
34	chr15:79261496-79261546	Caco-2	colon:	n/a
35	chr15:79269735-79269785	Caco-2	colon:	n/a
36	chr15:79298234-79298284	GM19239	blood:	n/a
37	chr15:79296424-79296474	NHDF-neo	bronchial:	n/a
38	chr15:79298691-79298741	HCPEpiC	choroid plexus:	n/a
39	chr15:79262857-79262907	AoSMC	blood vessel:	n/a
40	chr15:79296446-79296496	HRPEpiC	eye:	n/a
41	chr15:79297210-79297260	ProgFib	skin:	n/a
42	chr15:79254338-79254388	HMEC	breast:	n/a
43	chr15:79298604-79298654	IMR90	lung:	fetal
44	chr15:79252815-79252865	GM06990	blood:	n/a
45	chr15:79298678-79298728	AG10803	skin:	n/a
46	chr15:79254338-79254388	ovcar-3	ovarian:	n/a
47	chr15:79298637-79298687	SK-N-SH_RA	brain:	n/a
48	chr15:79297159-79297209	SK-N-SH	brain:	n/a
49	chr15:79298637-79298687	HUVEC	blood vessel:	n/a
50	chr15:79298606-79298656	HRCEpiC	kidney:	n/a

(count:94 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:79266861..79270074-chr15:79272087..79274367,3	K562	blood:
2	chr15:79308110..79311093-chr15:79312546..79314268,2	K562	blood:
3	chr15:79272649..79275133-chr15:79307482..79309069,2	MCF-7	breast:
4	chr15:79210945..79212489-chr15:79244847..79247301,2	K562	blood:
5	chr15:79276962..79279536-chr15:79281600..79283926,2	MCF-7	breast:
6	chr15:79255321..79258216-chr15:79260787..79263775,3	K562	blood:
7	chr15:79218320..79219259-chr15:79271509..79272622,7	MCF-7	breast:
8	chr15:79284397..79285995-chr15:79309750..79311999,2	MCF-7	breast:
9	chr15:79264133..79265722-chr15:79266216..79269027,2	MCF-7	breast:
10	chr15:79268574..79270778-chr15:79272295..79274532,2	K562	blood:
11	chr15:79277578..79279918-chr15:79282302..79283905,2	K562	blood:
12	chr15:79309558..79311093-chr15:79311925..79314268,2	K562	blood:
13	chr15:79236013..79238482-chr15:79249044..79251772,2	MCF-7	breast:
14	chr15:79239217..79242076-chr15:79246851..79248986,2	MCF-7	breast:
15	chr15:79255321..79258216-chr15:79260787..79263775,3	K562	blood:
16	chr15:79244340..79246222-chr15:79252129..79254810,2	K562	blood:
17	chr15:79202438..79205063-chr15:79282495..79284032,2	MCF-7	breast:
18	chr15:79286840..79288798-chr15:79290749..79294640,3	MCF-7	breast:
19	chr15:79278181..79281070-chr15:79299396..79302014,2	K562	blood:
20	chr15:79308342..79308897-chr15:79320983..79321915,2	MCF-7	breast:
21	chr15:79244340..79246222-chr15:79252129..79254810,2	K562	blood:
22	chr15:79217200..79220348-chr15:79270743..79273551,3	MCF-7	breast:
23	chr15:79289665..79292067-chr15:79295332..79297530,2	MCF-7	breast:
24	chr15:79289963..79292503-chr15:79300992..79303381,2	MCF-7	breast:
25	chr15:79164464..79167320-chr15:79273608..79277179,4	K562	blood:
26	chr15:79287783..79290330-chr15:79294942..79296932,2	MCF-7	breast:
27	chr15:79264133..79265722-chr15:79266216..79269027,2	MCF-7	breast:
28	chr15:79272649..79275133-chr15:79307482..79309069,2	MCF-7	breast:
29	chr15:79286840..79288798-chr15:79290749..79294640,3	MCF-7	breast:
30	chr15:79223166..79226414-chr15:79279938..79282218,3	MCF-7	breast:
31	chr15:79274407..79277285-chr15:79277913..79280154,2	K562	blood:
32	chr15:79206090..79206967-chr15:79271525..79272450,5	MCF-7	breast:
33	chr15:79243049..79243885-chr15:87130991..87131736,2	MCF-7	breast:
34	chr15:79264809..79266963-chr15:79270255..79272763,3	K562	blood:
35	chr15:79264746..79267610-chr15:79274625..79276620,2	K562	blood:
36	chr15:79238426..79240913-chr15:79263614..79265466,3	MCF-7	breast:
37	chr15:79272849..79274455-chr15:79275680..79277693,2	K562	blood:
38	chr15:79287783..79290330-chr15:79294942..79296932,2	MCF-7	breast:
39	chr15:79284397..79285995-chr15:79309750..79311999,2	MCF-7	breast:
40	chr15:79265663..79268823-chr15:79268915..79271641,3	K562	blood:
41	chr15:79242281..79244797-chr15:79245388..79247150,2	K562	blood:
42	chr15:79199697..79200212-chr15:79271797..79272673,2	MCF-7	breast:
43	chr15:79221775..79223364-chr15:79294791..79297170,2	MCF-7	breast:
44	chr15:79218551..79219226-chr15:79271642..79272206,2	MCF-7	breast:
45	chr15:79283718..79286389-chr15:79307664..79309741,2	K562	blood:
46	chr15:79274591..79277278-chr15:79290967..79292503,2	K562	blood:
47	chr15:79200123..79202028-chr15:79275613..79277156,2	MCF-7	breast:
48	chr15:79268574..79270778-chr15:79272295..79274532,2	K562	blood:
49	chr15:79306775..79309095-chr15:79315071..79317127,2	MCF-7	breast:
50	chr15:79198022..79200286-chr15:79243264..79245188,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RASGRF1-3	chr15:79251958-79252234	NONHSAT047631
2	lnc-RASGRF1-3	chr15:79249224-79249262	NONHSAT047631
3	lnc-RASGRF1-2	chr15:79252289-79253391	NONHSAT047632

No data

Variant related genes	Relation type
ENSG00000177699	TF binding region
RASGRF1	TF binding region
CTSH	TF binding region
ENSG00000177699	CpG island
RASGRF1	CpG island
CTSH	CpG island
ENSG00000177699	chromatin interactions
ENSG00000058335	chromatin interactions
ENSG00000185787	chromatin interactions
ENSG00000233396	chromatin interactions
ENSG00000103811	chromatin interactions

Extended variants
information (count: 2815 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2815 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs876941	chr15:79243571-79243572	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs77972579	chr15:79243576-79243577	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs534721690	chr15:79243600-79243601	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs570360438	chr15:79243607-79243608	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs376875522	chr15:79243636-79243637	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs16970350	chr15:79243674-79243675	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs571242217	chr15:79243678-79243679	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs139383236	chr15:79243685-79243686	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs35346837	chr15:79243731-79243732	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs144822255	chr15:79243734-79243735	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs397697117	chr15:79243738-79243739	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs140538429	chr15:79243795-79243796	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs567049319	chr15:79243818-79243819	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs536032765	chr15:79243845-79243846	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs555979011	chr15:79243859-79243860	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs568822888	chr15:79243861-79243862	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs576220199	chr15:79243893-79243894	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs536988049	chr15:79243930-79243931	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs113122588	chr15:79244028-79244029	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs558654077	chr15:79244031-79244032	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs572422099	chr15:79244033-79244034	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs185125169	chr15:79244044-79244045	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs11072819	chr15:79244071-79244072	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs374916182	chr15:79244101-79244102	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs78644681	chr15:79244112-79244113	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs62013234	chr15:79244147-79244148	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs575034220	chr15:79244164-79244165	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs544022263	chr15:79244236-79244237	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs137963530	chr15:79244261-79244262	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs28590490	chr15:79244312-79244313	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs78850476	chr15:79244338-79244339	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs572947720	chr15:79244384-79244385	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs559828637	chr15:79244396-79244397	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs372740113	chr15:79244406-79244407	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs116408691	chr15:79244453-79244454	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs541848258	chr15:79244496-79244497	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs190607460	chr15:79244542-79244543	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs184237475	chr15:79244586-79244587	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs188738699	chr15:79244594-79244595	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs73472328	chr15:79244611-79244612	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs549520381	chr15:79244614-79244615	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs569857459	chr15:79244624-79244625	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs192022930	chr15:79244655-79244656	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs182962068	chr15:79244680-79244681	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs187398430	chr15:79244693-79244694	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs143104922	chr15:79244721-79244722	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs112000400	chr15:79244740-79244741	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs371518977	chr15:79244741-79244742	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs550663893	chr15:79244748-79244749	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs191810980	chr15:79244767-79244768	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16774939	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:79237800-79243600	Weak transcription	Right Atrium	heart
2	chr15:79237800-79243600	Weak transcription	Spleen	Spleen
3	chr15:79237800-79244200	Weak transcription	Psoas Muscle	Psoas
4	chr15:79238600-79244200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr15:79238600-79252600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr15:79239000-79243600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr15:79240800-79245400	Enhancers	Stomach Mucosa	stomach
8	chr15:79241000-79245200	Enhancers	Liver	Liver
9	chr15:79241600-79244000	Enhancers	NHEK	skin
10	chr15:79241600-79244200	Enhancers	Gastric	stomach
11	chr15:79241600-79245000	Enhancers	Pancreas	Pancrea
12	chr15:79241800-79244800	Enhancers	Fetal Intestine Large	intestine
13	chr15:79242000-79245400	Enhancers	Duodenum Mucosa	Duodenum
14	chr15:79242200-79244400	Enhancers	Fetal Kidney	kidney
15	chr15:79242200-79244800	Enhancers	Lung	lung
16	chr15:79242400-79243800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr15:79242400-79244000	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr15:79242400-79244200	Enhancers	Skeletal Muscle Male	skeletal muscle
19	chr15:79242400-79244400	Enhancers	Adipose Nuclei	Adipose
20	chr15:79242400-79244800	Enhancers	Left Ventricle	heart
21	chr15:79242600-79244000	Weak transcription	Esophagus	oesophagus
22	chr15:79242600-79245000	Enhancers	Rectal Mucosa Donor 31	rectum
23	chr15:79242800-79243600	Weak transcription	Small Intestine	intestine
24	chr15:79242800-79243800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr15:79242800-79244000	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr15:79242800-79244200	Weak transcription	Fetal Intestine Small	intestine
27	chr15:79243000-79244600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr15:79243200-79243800	Flanking Active TSS	HepG2	liver
29	chr15:79243200-79244200	Enhancers	Fetal Muscle Leg	muscle
30	chr15:79243200-79244600	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr15:79243200-79244600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
32	chr15:79243200-79244600	Enhancers	A549	lung
33	chr15:79243200-79244600	Enhancers	GM12878-XiMat	blood
34	chr15:79243200-79244800	Enhancers	HMEC	breast
35	chr15:79243200-79245000	Enhancers	Primary B cells from peripheral blood	blood
36	chr15:79243200-79245000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr15:79243200-79245400	Enhancers	Hela-S3	cervix
38	chr15:79243400-79243800	Enhancers	Brain Substantia Nigra	brain
39	chr15:79243400-79243800	Enhancers	Right Ventricle	heart
40	chr15:79243400-79244200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr15:79243400-79244200	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr15:79243400-79244400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
43	chr15:79243400-79244600	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr15:79243400-79244600	Enhancers	Fetal Lung	lung
45	chr15:79243400-79244800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr15:79243400-79244800	Enhancers	Ovary	ovary
47	chr15:79243600-79243800	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr15:79243600-79243800	Enhancers	Spleen	Spleen
49	chr15:79243600-79244000	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr15:79243600-79244200	Enhancers	HUES48 Cell Line	embryonic stem cell

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