Variant report

Variant	rs545922049
Chromosome Location	chr9:139664585-139664586
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr9:139664500-139664650	GM12871	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664588-139664597 chr9:139664585-139664603
2	RAD21	chr9:139664471-139664654	SK-N-SH_RA	brain:	n/a	chr9:139664589-139664602 chr9:139664586-139664605 chr9:139664591-139664601 chr9:139664482-139664495 chr9:139664591-139664603 chr9:139664559-139664573 chr9:139664484-139664494
3	BHLHE40	chr9:139664520-139664614	GM12878	blood:	n/a	n/a
4	CTCFL	chr9:139664460-139664641	K562	blood:	n/a	chr9:139664592-139664601
5	CTCF	chr9:139664480-139664630	K562	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
6	CTCF	chr9:139664460-139664610	HEK293	kidney:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
7	CTCF	chr9:139664491-139664655	GM20000	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664588-139664597 chr9:139664585-139664603
8	CTCF	chr9:139664448-139664681	MCF-7	breast:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
9	TEAD4	chr9:139664338-139664645	K562	blood:	n/a	n/a
10	CTCF	chr9:139664271-139664724	K562	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
11	SMC3	chr9:139664492-139664627	GM12878	blood:	n/a	chr9:139664587-139664601 chr9:139664591-139664601 chr9:139664566-139664573
12	CTCF	chr9:139664480-139664630	AG04449	skin:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
13	UBTF	chr9:139664533-139664632	K562	blood:	n/a	n/a
14	CTCF	chr9:139664480-139664630	HBMEC	blood vessel:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
15	MAX	chr9:139664326-139664667	MCF-7	breast:	n/a	chr9:139664359-139664369
16	CTCF	chr9:139664480-139664630	AoAF	blood vessel:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
17	CTCF	chr9:139664480-139664630	GM12873	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
18	CTCF	chr9:139664453-139664679	ProgFib	skin:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
19	CTCF	chr9:139664426-139664705	A549	lung:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
20	CTCF	chr9:139664460-139664610	GM12874	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
21	CTCF	chr9:139664444-139664683	GM12878	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
22	MAX	chr9:139664270-139664722	A549	lung:	n/a	chr9:139664320-139664329 chr9:139664359-139664369
23	CTCF	chr9:139664480-139664630	AG10803	skin:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
24	ZNF143	chr9:139664409-139664642	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr9:139664460-139664610	GM12873	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
26	CTCF	chr9:139664459-139664651	A549	lung:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
27	CTCF	chr9:139664492-139664634	Lung_OC	lung:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664588-139664597 chr9:139664585-139664603
28	CTCF	chr9:139664500-139664650	NB4	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664588-139664597 chr9:139664585-139664603
29	MAX	chr9:139664328-139664662	K562	blood:	n/a	chr9:139664359-139664369
30	CTCF	chr9:139664500-139664650	HFF-Myc	foreskin:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664588-139664597 chr9:139664585-139664603
31	CTCF	chr9:139664480-139664630	NHEK	skin:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
32	CTCF	chr9:139664440-139664590	WI-38	lung:	n/a	chr9:139664483-139664493 chr9:139664481-139664494
33	CTCF	chr9:139664460-139664610	HMF	breast:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
34	RAD21	chr9:139664392-139664669	SK-N-SH_RA	brain:	n/a	chr9:139664589-139664602 chr9:139664586-139664605 chr9:139664591-139664601 chr9:139664482-139664495 chr9:139664591-139664603 chr9:139664559-139664573 chr9:139664484-139664494
35	CTCF	chr9:139664478-139664678	Hela-S3	cervix:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
36	CTCF	chr9:139664480-139664630	GM12878	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
37	FOXP2	chr9:139664402-139664650	PFSK-1	brain:	n/a	n/a
38	CTCF	chr9:139664500-139664650	GM12875	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664588-139664597 chr9:139664585-139664603
39	CTCF	chr9:139664461-139664703	A549	lung:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
40	JUND	chr9:139664435-139664587	H1-hESC	embryonic stem cell:	n/a	n/a
41	RAD21	chr9:139664394-139664634	HepG2	liver:	n/a	chr9:139664589-139664602 chr9:139664586-139664605 chr9:139664591-139664601 chr9:139664482-139664495 chr9:139664591-139664603 chr9:139664559-139664573 chr9:139664484-139664494
42	CTCF	chr9:139664440-139664698	GM10266	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
43	CTCF	chr9:139664460-139664610	GM12868	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
44	CTCF	chr9:139664500-139664650	GM12864	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664588-139664597 chr9:139664585-139664603
45	BHLHE40	chr9:139664410-139664615	K562	blood:	n/a	n/a
46	CTCF	chr9:139664500-139664650	BE2_C	brain:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664588-139664597 chr9:139664585-139664603
47	CTCF	chr9:139664500-139664650	HRPEpiC	eye:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664588-139664597 chr9:139664585-139664603
48	CTCF	chr9:139664478-139664659	Kidney_OC	kidney:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
49	CTCF	chr9:139664206-139664705	A549	lung:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
50	CTCF	chr9:139664438-139664704	H1-hESC	embryonic stem cell:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603

No.	Distal block	Cell Line	Cell type
1	chr9:139617845..139623838-chr9:139660350..139667246,10	K562	blood:
2	chr9:139656220..139657844-chr9:139664541..139666356,2	K562	blood:
3	chr9:139662310..139665146-chr9:139700169..139702660,2	K562	blood:
4	chr9:139662206..139666130-chr9:139666450..139670889,6	K562	blood:
5	chr9:139615454..139618647-chr9:139663629..139666598,3	MCF-7	breast:
6	chr9:139663003..139666035-chr9:139678378..139681076,3	MCF-7	breast:
7	chr9:139621278..139624827-chr9:139660350..139665047,5	K562	blood:
8	chr9:139663599..139665182-chr9:139742980..139744994,2	MCF-7	breast:
9	chr9:139640588..139643273-chr9:139662768..139664600,2	K562	blood:
10	chr9:139664152..139666690-chr9:139684867..139687116,2	MCF-7	breast:

Variant related genes	Relation type
LCN15	TF binding region
ENSG00000233016	Chromatin interaction
ENSG00000267206	Chromatin interaction
ENSG00000244187	Chromatin interaction
ENSG00000273066	Chromatin interaction
ENSG00000204003	Chromatin interaction
ENSG00000272896	Chromatin interaction
ENSG00000196642	Chromatin interaction
ENSG00000054148	Chromatin interaction
ENSG00000213213	Chromatin interaction

Extended variants
information (count: 57 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:57 , 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	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	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
26	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
27	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
28	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
29	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
30	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
31	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
32	nsv894445	chr9:139556771-139669111	Bivalent Enhancer Genic enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	145 gene(s)	inside rSNPs	diseases
33	nsv1043160	chr9:139560991-139665208	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	145 gene(s)	inside rSNPs	diseases
34	nsv540349	chr9:139560991-139665208	Genic enhancers Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Strong transcription 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
35	nsv894449	chr9:139598108-139669111	Genic enhancers Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	94 gene(s)	inside rSNPs	diseases
36	nsv894450	chr9:139598108-139776400	Active TSS Strong transcription Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	130 gene(s)	inside rSNPs	diseases
37	nsv894451	chr9:139598108-139995065	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	200 gene(s)	inside rSNPs	diseases
38	nsv894452	chr9:139598108-140523429	Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	450 gene(s)	inside rSNPs	diseases
39	nsv894454	chr9:139607966-139904037	Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	172 gene(s)	inside rSNPs	diseases
40	nsv894455	chr9:139607966-140411547	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers 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	417 gene(s)	inside rSNPs	diseases
41	nsv1051605	chr9:139620105-139728697	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	108 gene(s)	inside rSNPs	diseases
42	nsv540350	chr9:139620105-139728697	Bivalent Enhancer Genic enhancers Weak transcription Active TSS Enhancers Flanking Active TSS 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	108 gene(s)	inside rSNPs	diseases
43	nsv818738	chr9:139634495-139904037	Strong transcription Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	126 gene(s)	inside rSNPs	diseases
44	nsv466681	chr9:139647074-139693992	Genic enhancers Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
45	nsv615982	chr9:139647074-139693992	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
46	nsv818739	chr9:139648721-139669111	Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
47	nsv894456	chr9:139650448-139674527	Weak transcription Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
48	nsv894457	chr9:139650448-139776400	Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	79 gene(s)	inside rSNPs	diseases
49	esv3423612	chr9:139662556-139665504	Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
50	esv16622	chr9:139662736-139665108	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region Chromatin interactive region	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:139657800-139667800	Weak transcription	Right Atrium	heart
2	chr9:139659200-139667800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr9:139664000-139664600	Enhancers	Primary B cells from peripheral blood	blood
4	chr9:139664200-139664600	Active TSS	ES-I3 Cell Line	embryonic stem cell
5	chr9:139664200-139664600	Active TSS	H9 Cell Line	embryonic stem cell
6	chr9:139664200-139664600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr9:139664200-139664600	Active TSS	HUES48 Cell Line	embryonic stem cell
8	chr9:139664200-139664600	Active TSS	HUES6 Cell Line	embryonic stem cell
9	chr9:139664200-139664600	Active TSS	HUES64 Cell Line	embryonic stem cell
10	chr9:139664200-139664600	Active TSS	iPS-15b Cell Line	embryonic stem cell
11	chr9:139664200-139664600	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr9:139664200-139664600	Active TSS	iPS-20b Cell Line	embryonic stem cell
13	chr9:139664200-139664600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr9:139664200-139664600	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr9:139664200-139664600	Enhancers	Primary T cells from cord blood	blood
16	chr9:139664200-139664600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
17	chr9:139664200-139664600	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr9:139664200-139664600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
19	chr9:139664200-139664600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
20	chr9:139664200-139664600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
21	chr9:139664200-139664600	Enhancers	Primary T helper cells fromperipheralblood	blood
22	chr9:139664200-139664600	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
23	chr9:139664200-139664600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
24	chr9:139664200-139664600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr9:139664200-139664600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr9:139664200-139664600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
27	chr9:139664200-139664600	Enhancers	Fetal Intestine Large	intestine
28	chr9:139664200-139664600	Enhancers	Fetal Intestine Small	intestine
29	chr9:139664200-139664600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
30	chr9:139664200-139664600	Enhancers	Placenta	Placenta
31	chr9:139664200-139664600	Enhancers	Right Ventricle	heart
32	chr9:139664200-139664600	Enhancers	Stomach Mucosa	stomach
33	chr9:139664200-139664600	Active TSS	A549	lung
34	chr9:139664200-139664600	Enhancers	HepG2	liver
35	chr9:139664200-139664600	Enhancers	K562	blood
36	chr9:139664400-139664600	Flanking Active TSS	H1 Cell Line	embryonic stem cell
37	chr9:139664400-139664600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr9:139664400-139664600	Enhancers	Primary T helper cells PMA-I stimulated	--
39	chr9:139664400-139664600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr9:139664400-139664600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr9:139664400-139664600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr9:139664400-139664600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr9:139664400-139664600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
44	chr9:139664400-139664600	Enhancers	Colonic Mucosa	Colon
45	chr9:139664400-139664600	Bivalent Enhancer	Fetal Stomach	stomach
46	chr9:139664400-139664600	Enhancers	Fetal Thymus	thymus
47	chr9:139664400-139664600	Enhancers	Ovary	ovary
48	chr9:139664400-139664600	Enhancers	Pancreas	Pancrea
49	chr9:139664400-139664600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum

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