Variant report

Variant	rs536892257
Chromosome Location	chr11:67396858-67396859
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	POLR2A	chr11:67396741-67397537	HUVEC	blood vessel:	n/a	n/a
2	SMC3	chr11:67396635-67397116	GM12878	blood:	n/a	chr11:67396876-67396890 chr11:67396880-67396890
3	MYC	chr11:67396716-67397256	K562	blood:	n/a	chr11:67396965-67396974 chr11:67396969-67396985
4	CTCF	chr11:67396800-67396950	HUVEC	blood vessel:	n/a	chr11:67396874-67396892 chr11:67396875-67396891 chr11:67396844-67396857 chr11:67396877-67396890
5	MAX	chr11:67396745-67397505	K562	blood:	n/a	chr11:67396965-67396974 chr11:67396969-67396985 chr11:67397409-67397419
6	CTCF	chr11:67396800-67396950	HCFaa	heart:	n/a	chr11:67396874-67396892 chr11:67396875-67396891 chr11:67396844-67396857 chr11:67396877-67396890
7	ZBTB7A	chr11:67396605-67397177	K562	blood:	n/a	n/a
8	CTCF	chr11:67396454-67397453	HCT-116	colon:	n/a	chr11:67396874-67396892 chr11:67396875-67396891 chr11:67396844-67396857 chr11:67396877-67396890
9	E2F6	chr11:67396632-67397690	A549	lung:	n/a	chr11:67396905-67396912 chr11:67396902-67396913 chr11:67396905-67396912 chr11:67396905-67396912
10	POLR2A	chr11:67396647-67397536	HepG2	liver:	n/a	n/a
11	POLR2A	chr11:67393312-67402949	H1-hESC	embryonic stem cell:	n/a	n/a
12	CREB1	chr11:67396714-67398507	K562	blood:	n/a	n/a
13	RFX5	chr11:67396795-67396938	H1-hESC	embryonic stem cell:	n/a	chr11:67396803-67396812
14	TCF12	chr11:67396810-67397171	GM12878	blood:	n/a	n/a
15	CTCFL	chr11:67396791-67397016	K562	blood:	n/a	chr11:67396881-67396890
16	UBTF	chr11:67396753-67397564	K562	blood:	n/a	n/a
17	CTCF	chr11:67396840-67396990	BE2_C	brain:	n/a	chr11:67396874-67396892 chr11:67396875-67396891 chr11:67396844-67396857 chr11:67396877-67396890
18	MAX	chr11:67396752-67397567	Hela-S3	cervix:	n/a	chr11:67396965-67396974 chr11:67396969-67396985 chr11:67397409-67397419
19	RAD21	chr11:67396613-67397109	H1-hESC	embryonic stem cell:	n/a	chr11:67396875-67396894 chr11:67396878-67396891 chr11:67396880-67396890 chr11:67396880-67396892
20	RCOR1	chr11:67396364-67397780	IMR90	lung:	n/a	n/a
21	RAD21	chr11:67396521-67397549	SK-N-SH	brain:	n/a	chr11:67396875-67396894 chr11:67396878-67396891 chr11:67396880-67396890 chr11:67396880-67396892
22	RAD21	chr11:67396481-67397271	HCT-116	colon:	n/a	chr11:67396875-67396894 chr11:67396878-67396891 chr11:67396880-67396890 chr11:67396880-67396892
23	CTCF	chr11:67396760-67396910	HRE	kidney:	n/a	chr11:67396874-67396892 chr11:67396875-67396891 chr11:67396844-67396857 chr11:67396877-67396890
24	FOXM1	chr11:67396626-67397139	GM12878	blood:	n/a	n/a
25	EP300	chr11:67396777-67397066	GM12878	blood:	n/a	chr11:67396883-67396892
26	POLR2A	chr11:67396819-67397638	A549	lung:	n/a	n/a
27	NRF1	chr11:67396641-67397018	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chr11:67396642-67397138	GM12878	blood:	n/a	n/a
29	HEY1	chr11:67396701-67397609	HepG2	liver:	n/a	n/a
30	RCOR1	chr11:67396694-67397426	K562	blood:	n/a	n/a
31	POLR2A	chr11:67396744-67397637	GM12878	blood:	n/a	n/a
32	CTCF	chr11:67396800-67396950	HA-sp	spinal cord:	n/a	chr11:67396874-67396892 chr11:67396875-67396891 chr11:67396844-67396857 chr11:67396877-67396890
33	BCLAF1	chr11:67396581-67397187	GM12878	blood:	n/a	chr11:67396585-67396598
34	E2F6	chr11:67396696-67397730	K562	blood:	n/a	chr11:67396905-67396912 chr11:67396902-67396913 chr11:67396905-67396912 chr11:67396905-67396912
35	RAD21	chr11:67396704-67397058	HepG2	liver:	n/a	chr11:67396875-67396894 chr11:67396878-67396891 chr11:67396880-67396890 chr11:67396880-67396892
36	CTCF	chr11:67396544-67397077	HepG2	liver:	n/a	chr11:67396874-67396892 chr11:67396875-67396891 chr11:67396844-67396857 chr11:67396877-67396890
37	SP1	chr11:67396771-67397174	A549	lung:	n/a	chr11:67396846-67396858 chr11:67396848-67396857 chr11:67396882-67396894 chr11:67396882-67396894
38	PAX5	chr11:67396777-67397651	GM12892	blood:	n/a	chr11:67397014-67397033
39	CTCF	chr11:67396780-67396930	HPF	lung:	n/a	chr11:67396874-67396892 chr11:67396875-67396891 chr11:67396844-67396857 chr11:67396877-67396890
40	ZBTB7A	chr11:67396758-67397746	ECC-1	luminal epithelium:	n/a	n/a
41	CTCF	chr11:67396780-67396930	AoAF	blood vessel:	n/a	chr11:67396874-67396892 chr11:67396875-67396891 chr11:67396844-67396857 chr11:67396877-67396890
42	SIN3AK20	chr11:67396687-67396993	A549	lung:	n/a	n/a
43	REST	chr11:67396814-67397268	A549	lung:	n/a	n/a
44	POLR2A	chr11:67396344-67397101	K562	blood:	n/a	n/a
45	PAX5	chr11:67396764-67397280	GM12878	blood:	n/a	chr11:67397014-67397033
46	CTCF	chr11:67396800-67396950	HPAF	blood vessel:	n/a	chr11:67396874-67396892 chr11:67396875-67396891 chr11:67396844-67396857 chr11:67396877-67396890
47	POLR2A	chr11:67396626-67397602	K562	blood:	n/a	n/a
48	FOXA2	chr11:67396736-67397098	A549	lung:	n/a	n/a
49	CTCF	chr11:67396760-67397009	Hela-S3	cervix:	n/a	chr11:67396874-67396892 chr11:67396875-67396891 chr11:67396844-67396857 chr11:67396877-67396890
50	CTCF	chr11:67396780-67396930	GM12866	blood:	n/a	chr11:67396874-67396892 chr11:67396875-67396891 chr11:67396844-67396857 chr11:67396877-67396890

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:67396845-67396895	PANC-1	pancreas:	n/a
2	chr11:67396845-67396895	SAEC	small airway:	n/a
3	chr11:67396845-67396895	HPAEpiC	pulmonary alveolar:	n/a
4	chr11:67396845-67396895	AG04450	lung:	fetal
5	chr11:67396845-67396895	NHBE	bronchial:	n/a
6	chr11:67396845-67396895	HCM	heart:	n/a
7	chr11:67396845-67396895	MCF-7	breast:	n/a
8	chr11:67396845-67396895	HAEpiC	amniotic membrane:	n/a
9	chr11:67396845-67396895	PFSK-1	brain:	n/a
10	chr11:67396845-67396895	HepG2	liver:	n/a
11	chr11:67396845-67396895	GM12891	blood:	n/a
12	chr11:67396845-67396895	BJ	skin:	n/a
13	chr11:67396845-67396895	HCPEpiC	choroid plexus:	n/a
14	chr11:67396845-67396895	GM19239	blood:	n/a
15	chr11:67396845-67396895	PrEC	prostate:	n/a
16	chr11:67396845-67396895	NHDF-neo	bronchial:	n/a
17	chr11:67396845-67396895	NT2-D1	testis:	n/a
18	chr11:67396845-67396895	SKMC	muscle:	n/a
19	chr11:67396845-67396895	IMR90	lung:	fetal
20	chr11:67396845-67396895	Hela-S3	cervix:	n/a
21	chr11:67396845-67396895	NH-A	brain:	n/a
22	chr11:67396845-67396895	A549	lung:	n/a
23	chr11:67396845-67396895	HMEC	breast:	n/a
24	chr11:67396845-67396895	HRCEpiC	kidney:	n/a
25	chr11:67396845-67396895	GM12892	blood:	n/a
26	chr11:67396845-67396895	AG09319	gingival:	n/a
27	chr11:67396845-67396895	Jurkat	blood:	n/a
28	chr11:67396845-67396895	U87	brain:	n/a
29	chr11:67396845-67396895	LNCaP	prostate:	n/a
30	chr11:67396845-67396895	GM12878	blood:	n/a
31	chr11:67396845-67396895	ECC-1	luminal epithelium:	n/a
32	chr11:67396845-67396895	HCT-116	colon:	n/a
33	chr11:67396845-67396895	HRE	kidney:	n/a
34	chr11:67396845-67396895	CMK	blood:	n/a
35	chr11:67396845-67396895	ovcar-3	ovarian:	n/a
36	chr11:67396845-67396895	Caco-2	colon:	n/a
37	chr11:67396845-67396895	Hepatocyte	liver:	n/a
38	chr11:67396845-67396895	HEEpiC	esophagus:	n/a
39	chr11:67396845-67396895	AG04449	skin:	fetal
40	chr11:67396845-67396895	GM06990	blood:	n/a
41	chr11:67396845-67396895	AoSMC	blood vessel:	n/a
42	chr11:67396845-67396895	AG09309	skin:	n/a
43	chr11:67396845-67396895	H1-hESC	embryonic stem cell:	embryo
44	chr11:67396845-67396895	BE2_C	brain:	n/a
45	chr11:67396845-67396895	NB4	blood:	n/a
46	chr11:67396845-67396895	SK-N-SH	brain:	n/a
47	chr11:67396845-67396895	ProgFib	skin:	n/a
48	chr11:67396845-67396895	HUVEC	blood vessel:	n/a
49	chr11:67396845-67396895	K562	blood:	n/a
50	chr11:67396845-67396895	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:67396434..67397233-chr11:67415377..67416192,2	MCF-7	breast:
2	chr11:67395178..67397377-chr6:27100620..27102983,2	K562	blood:
3	chr11:67381470..67382086-chr11:67396612..67397307,2	MCF-7	breast:
4	chr11:67395494..67399201-chr11:67413492..67416311,3	K562	blood:
5	chr11:67140815..67142437-chr11:67396749..67399508,2	MCF-7	breast:
6	chr11:67373358..67378331-chr11:67393882..67398214,7	MCF-7	breast:
7	chr11:67372725..67386378-chr11:67392399..67400639,29	K562	blood:
8	chr11:67225796..67227949-chr11:67395542..67397304,2	K562	blood:
9	chr11:67380957..67389846-chr11:67394173..67403228,21	K562	blood:
10	chr11:67396418..67397288-chr17:19669617..19670437,3	MCF-7	breast:
11	chr11:67396543..67400484-chr11:67414425..67419634,5	MCF-7	breast:
12	chr11:67344360..67352769-chr11:67395394..67400721,12	K562	blood:
13	chr11:67157781..67159663-chr11:67396161..67398201,2	K562	blood:
14	chr11:67396772..67397765-chr5:180236385..180237144,2	Hela-S3	cervix:
15	chr11:67371375..67376389-chr11:67395488..67399117,10	K562	blood:
16	chr11:67308127..67309699-chr11:67395126..67397854,2	K562	blood:
17	chr11:67046781..67048782-chr11:67395418..67397975,2	K562	blood:
18	chr10:14920177..14922925-chr11:67396775..67398999,2	MCF-7	breast:
19	chr11:67395852..67400432-chr11:67404620..67408941,6	K562	blood:
20	chr11:67395020..67397974-chr11:67571574..67573157,2	MCF-7	breast:
21	chr11:67188329..67190078-chr11:67395497..67397471,2	K562	blood:
22	chr11:67396324..67397202-chr11:67407117..67407748,3	MCF-7	breast:
23	chr11:67377022..67387637-chr11:67394926..67400114,17	MCF-7	breast:
24	chr11:66885940..66887950-chr11:67395860..67397869,2	K562	blood:
25	chr11:67140319..67142184-chr11:67395845..67397635,2	MCF-7	breast:
26	chr11:67348847..67353254-chr11:67396059..67399206,10	K562	blood:
27	chr11:67396464..67397218-chr11:67465404..67466018,2	MCF-7	breast:
28	chr11:67378665..67384491-chr11:67395408..67398335,5	MCF-7	breast:
29	chr11:67370584..67375680-chr11:67395595..67400853,11	MCF-7	breast:
30	chr11:67396168..67397948-chr11:67571471..67573438,2	K562	blood:

Variant related genes	Relation type
ENSG00000255318	TF binding region
ENSG00000255318	CpG island
ENSG00000244152	Chromatin interaction
ENSG00000172531	Chromatin interaction
ENSG00000196787	Chromatin interaction
ENSG00000173020	Chromatin interaction
ENSG00000152455	Chromatin interaction
ENSG00000255119	Chromatin interaction
ENSG00000132744	Chromatin interaction
ENSG00000167800	Chromatin interaction
ENSG00000184224	Chromatin interaction
ENSG00000175505	Chromatin interaction
ENSG00000272853	Chromatin interaction
ENSG00000160172	Chromatin interaction
ENSG00000256514	Chromatin interaction
ENSG00000269913	Chromatin interaction
ENSG00000131446	Chromatin interaction
ENSG00000167792	Chromatin interaction
ENSG00000173120	Chromatin interaction
ENSG00000172508	Chromatin interaction
ENSG00000084207	Chromatin interaction
ENSG00000231793	Chromatin interaction
ENSG00000172613	Chromatin interaction

Extended variants
information (count: 44 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:44 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531397	chr11:66653381-67465721	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
2	nsv897801	chr11:67033076-67432479	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats 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	236 gene(s)	inside rSNPs	diseases
3	nsv897807	chr11:67155210-67414492	Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer 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	176 gene(s)	inside rSNPs	diseases
4	nsv897808	chr11:67155210-67419855	Flanking Active TSS Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
5	nsv534229	chr11:67164667-67411909	Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	175 gene(s)	inside rSNPs	diseases
6	esv2422195	chr11:67234322-67626901	Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Weak 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	146 gene(s)	inside rSNPs	diseases
7	nsv1041988	chr11:67319916-67749246	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
8	nsv897814	chr11:67339949-67460529	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
9	nsv1050463	chr11:67343421-67717338	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
10	nsv1038189	chr11:67345320-67749246	Transcr. at gene 5' and 3' Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
11	nsv1047236	chr11:67345320-67764068	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription 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 target site	83 gene(s)	inside rSNPs	diseases
12	nsv555268	chr11:67346743-67752972	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
13	nsv1036101	chr11:67346813-67828351	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
14	nsv541079	chr11:67346813-67828351	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
15	nsv897815	chr11:67347595-67408791	Enhancers Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
16	nsv1053811	chr11:67349444-67749246	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
17	esv1817852	chr11:67349899-67626567	Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Weak transcription Bivalent Enhancer 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 target site	69 gene(s)	inside rSNPs	diseases
18	nsv468606	chr11:67352689-67816936	Active TSS Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
19	nsv555269	chr11:67352689-67816936	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
20	nsv897816	chr11:67353579-67460529	Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
21	nsv1041887	chr11:67357365-67464893	Flanking Active TSS Genic enhancers Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
22	nsv541080	chr11:67357365-67464893	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
23	nsv529452	chr11:67358204-67465721	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer 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	49 gene(s)	inside rSNPs	diseases
24	nsv492253	chr11:67358204-67574402	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	65 gene(s)	inside rSNPs	diseases
25	nsv1043487	chr11:67360899-67662476	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	71 gene(s)	inside rSNPs	diseases
26	nsv897817	chr11:67372477-67414492	Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
27	nsv897818	chr11:67372477-67419855	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
28	nsv468607	chr11:67372477-67423892	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer 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
29	nsv555270	chr11:67372477-67423892	Enhancers Active TSS Flanking Active TSS Genic enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
30	nsv897819	chr11:67372477-67426797	Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
31	nsv468608	chr11:67372477-67433869	Genic enhancers Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
32	nsv555271	chr11:67372477-67433869	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
33	nsv897820	chr11:67372477-67460529	Flanking Active TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
34	nsv897821	chr11:67378594-67430762	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
35	nsv897822	chr11:67378594-67441553	Genic enhancers Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
36	nsv897823	chr11:67378594-67460529	Enhancers Bivalent Enhancer Active TSS Genic enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
37	nsv897824	chr11:67379575-67418202	Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Enhancers Genic enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	40 gene(s)	inside rSNPs	diseases
38	nsv897825	chr11:67381110-67460529	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
39	nsv555272	chr11:67394895-67408241	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	39 gene(s)	inside rSNPs	diseases
40	nsv468609	chr11:67395714-67433869	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
41	nsv555273	chr11:67395714-67433869	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
42	nsv469963	chr11:67395714-67438195	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
43	esv3390228	chr11:67396401-67399249	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	37 gene(s)	inside rSNPs	diseases
44	esv3352142	chr11:67396776-67398924	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	37 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67379600-67397000	Weak transcription	Aorta	Aorta
2	chr11:67390600-67397000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr11:67390600-67397000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr11:67395000-67397000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr11:67395600-67397200	Enhancers	Fetal Heart	heart
6	chr11:67396000-67397000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
7	chr11:67396000-67397000	Enhancers	Fetal Thymus	thymus
8	chr11:67396000-67397200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr11:67396000-67398200	Active TSS	Hela-S3	cervix
10	chr11:67396000-67398800	Active TSS	H9 Cell Line	embryonic stem cell
11	chr11:67396200-67397000	Enhancers	Primary B cells from cord blood	blood
12	chr11:67396200-67397000	Enhancers	Placenta	Placenta
13	chr11:67396200-67397200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
14	chr11:67396200-67397400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
15	chr11:67396400-67397000	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr11:67396400-67397000	Enhancers	Primary hematopoietic stem cells	blood
17	chr11:67396400-67397000	Enhancers	Spleen	Spleen
18	chr11:67396400-67397200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr11:67396400-67397400	Flanking Active TSS	Colonic Mucosa	Colon
20	chr11:67396400-67397400	Flanking Active TSS	HMEC	breast
21	chr11:67396400-67398400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr11:67396600-67397000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
23	chr11:67396600-67397000	Enhancers	Primary T helper naive cells from peripheral blood	blood
24	chr11:67396600-67397000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
25	chr11:67396600-67397200	Flanking Active TSS	Primary B cells from peripheral blood	blood
26	chr11:67396600-67397200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr11:67396600-67397200	Flanking Active TSS	Brain Germinal Matrix	brain
28	chr11:67396600-67397200	Flanking Active TSS	Stomach Mucosa	stomach
29	chr11:67396600-67397400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
30	chr11:67396600-67397400	Flanking Active TSS	Stomach Smooth Muscle	stomach
31	chr11:67396600-67397400	Flanking Active TSS	Dnd41	blood
32	chr11:67396600-67398200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr11:67396600-67398200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr11:67396600-67398200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr11:67396600-67398200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr11:67396600-67398200	Active TSS	Brain Anterior Caudate	brain
37	chr11:67396600-67398400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr11:67396600-67398400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr11:67396600-67398400	Active TSS	HUES6 Cell Line	embryonic stem cell
40	chr11:67396600-67398400	Active TSS	iPS-20b Cell Line	embryonic stem cell
41	chr11:67396600-67398400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr11:67396600-67398400	Active TSS	Rectal Smooth Muscle	rectum
43	chr11:67396600-67398400	Active TSS	NHDF-Ad	bronchial
44	chr11:67396600-67398800	Active TSS	HUES64 Cell Line	embryonic stem cell
45	chr11:67396600-67398800	Active TSS	HSMM	muscle
46	chr11:67396800-67397000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr11:67396800-67397000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
48	chr11:67396800-67397000	Active TSS	Primary T helper cells PMA-I stimulated	--
49	chr11:67396800-67397000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr11:67396800-67397000	Active TSS	Duodenum Mucosa	Duodenum

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