Variant report

Variant	rs10707247
Chromosome Location	chr8:1771238-1771239
allele	-/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	MAFK	chr8:1771052-1771387	H1-hESC	embryonic stem cell:	n/a	chr8:1771171-1771186 chr8:1771170-1771184 chr8:1771171-1771187 chr8:1771171-1771182 chr8:1771171-1771182
2	SP1	chr8:1771161-1772405	HCT-116	colon:	n/a	chr8:1771785-1771794 chr8:1771783-1771795 chr8:1771784-1771793 chr8:1771866-1771878 chr8:1771866-1771878 chr8:1772088-1772102 chr8:1771639-1771650 chr8:1772017-1772038 chr8:1771785-1771794 chr8:1771780-1771794 chr8:1771867-1771876
3	MAFF	chr8:1771019-1771365	K562	blood:	n/a	chr8:1771169-1771187
4	MYC	chr8:1770915-1771520	MCF10A-Er-Src	breast:	n/a	n/a
5	MAX	chr8:1771185-1772290	H1-hESC	embryonic stem cell:	n/a	chr8:1771949-1771962 chr8:1771950-1771960 chr8:1771614-1771624 chr8:1771949-1771962 chr8:1771951-1771960 chr8:1771562-1771572 chr8:1771950-1771960 chr8:1771951-1771961 chr8:1771950-1771961 chr8:1771950-1771961 chr8:1771951-1771961 chr8:1771891-1771901 chr8:1771950-1771961 chr8:1771640-1771650
6	POLR2A	chr8:1770733-1772156	MCF10A-Er-Src	breast:	n/a	n/a
7	STAT3	chr8:1771036-1771525	MCF10A-Er-Src	breast:	n/a	n/a
8	POLR2A	chr8:1771161-1772213	HUVEC	blood vessel:	n/a	n/a
9	MXI1	chr8:1771138-1772183	IMR90	lung:	n/a	chr8:1771950-1771959 chr8:1771952-1771961 chr8:1771950-1771959 chr8:1771952-1771961
10	POLR2A	chr8:1771157-1772326	HUVEC	blood vessel:	n/a	n/a
11	STAT3	chr8:1771062-1771504	MCF10A-Er-Src	breast:	n/a	n/a
12	SP1	chr8:1771215-1772130	H1-hESC	embryonic stem cell:	n/a	chr8:1771785-1771794 chr8:1771783-1771795 chr8:1771784-1771793 chr8:1771866-1771878 chr8:1771866-1771878 chr8:1772088-1772102 chr8:1771639-1771650 chr8:1772017-1772038 chr8:1771785-1771794 chr8:1771780-1771794 chr8:1771867-1771876
13	MYC	chr8:1771178-1772122	A549	lung:	n/a	chr8:1771949-1771962 chr8:1771950-1771960 chr8:1771614-1771624 chr8:1771949-1771962 chr8:1771951-1771960 chr8:1771562-1771572 chr8:1771950-1771960 chr8:1771951-1771961 chr8:1771950-1771961 chr8:1771950-1771961 chr8:1771951-1771961 chr8:1771891-1771901 chr8:1771950-1771961 chr8:1771640-1771650
14	MAX	chr8:1771189-1772195	SK-N-SH	brain:	n/a	chr8:1771949-1771962 chr8:1771950-1771960 chr8:1771614-1771624 chr8:1771949-1771962 chr8:1771951-1771960 chr8:1771562-1771572 chr8:1771950-1771960 chr8:1771951-1771961 chr8:1771950-1771961 chr8:1771950-1771961 chr8:1771951-1771961 chr8:1771891-1771901 chr8:1771950-1771961 chr8:1771640-1771650
15	ZMIZ1	chr8:1771224-1771379	K562	blood:	n/a	n/a
16	MAX	chr8:1771147-1772200	ECC-1	luminal epithelium:	n/a	chr8:1771949-1771962 chr8:1771950-1771960 chr8:1771614-1771624 chr8:1771949-1771962 chr8:1771951-1771960 chr8:1771562-1771572 chr8:1771950-1771960 chr8:1771951-1771961 chr8:1771950-1771961 chr8:1771950-1771961 chr8:1771951-1771961 chr8:1771891-1771901 chr8:1771950-1771961 chr8:1771640-1771650
17	RCOR1	chr8:1771227-1772085	Hela-S3	cervix:	n/a	n/a
18	MAFK	chr8:1771003-1771351	HepG2	liver:	n/a	chr8:1771171-1771186 chr8:1771170-1771184 chr8:1771171-1771187 chr8:1771171-1771182 chr8:1771171-1771182
19	MAX	chr8:1771135-1772326	ECC-1	luminal epithelium:	n/a	chr8:1771949-1771962 chr8:1771950-1771960 chr8:1771614-1771624 chr8:1771949-1771962 chr8:1771951-1771960 chr8:1771562-1771572 chr8:1771950-1771960 chr8:1771951-1771961 chr8:1771950-1771961 chr8:1771950-1771961 chr8:1771951-1771961 chr8:1771891-1771901 chr8:1771950-1771961 chr8:1771640-1771650
20	JUND	chr8:1771202-1771525	K562	blood:	n/a	chr8:1771481-1771495
21	MAFF	chr8:1771029-1771313	HepG2	liver:	n/a	chr8:1771169-1771187
22	RFX5	chr8:1771010-1772165	Hela-S3	cervix:	n/a	chr8:1771992-1772006
23	HCFC1	chr8:1771124-1772355	Hela-S3	cervix:	n/a	n/a
24	STAT3	chr8:1771025-1771528	MCF10A-Er-Src	breast:	n/a	n/a
25	POLR2A	chr8:1771184-1772671	IMR90	lung:	n/a	n/a
26	POLR2A	chr8:1771228-1772153	HUVEC	blood vessel:	n/a	n/a
27	ZBTB7A	chr8:1771237-1772888	ECC-1	luminal epithelium:	n/a	chr8:1771812-1771821 chr8:1771937-1771946 chr8:1771731-1771738 chr8:1771887-1771896
28	MYC	chr8:1770856-1772169	MCF10A-Er-Src	breast:	n/a	chr8:1771949-1771962 chr8:1771950-1771960 chr8:1771614-1771624 chr8:1771949-1771962 chr8:1771951-1771960 chr8:1771562-1771572 chr8:1771950-1771960 chr8:1771951-1771961 chr8:1771950-1771961 chr8:1771950-1771961 chr8:1771951-1771961 chr8:1771891-1771901 chr8:1771950-1771961 chr8:1771640-1771650
29	MAX	chr8:1771110-1772330	HCT-116	colon:	n/a	chr8:1771949-1771962 chr8:1771950-1771960 chr8:1771614-1771624 chr8:1771949-1771962 chr8:1771951-1771960 chr8:1771562-1771572 chr8:1771950-1771960 chr8:1771951-1771961 chr8:1771950-1771961 chr8:1771950-1771961 chr8:1771951-1771961 chr8:1771891-1771901 chr8:1771950-1771961 chr8:1771640-1771650
30	MAFK	chr8:1770985-1771551	IMR90	lung:	n/a	chr8:1771171-1771186 chr8:1771170-1771184 chr8:1771171-1771187 chr8:1771171-1771182 chr8:1771171-1771182
31	MAZ	chr8:1771104-1772835	IMR90	lung:	n/a	chr8:1771949-1771962 chr8:1771950-1771960 chr8:1772502-1772512 chr8:1771614-1771624 chr8:1771949-1771962 chr8:1771951-1771960 chr8:1771562-1771572 chr8:1771950-1771960 chr8:1771951-1771961 chr8:1771950-1771961 chr8:1771950-1771961 chr8:1771951-1771961 chr8:1771891-1771901 chr8:1771950-1771961 chr8:1771640-1771650
32	MAX	chr8:1771147-1772186	SK-N-SH	brain:	n/a	chr8:1771949-1771962 chr8:1771950-1771960 chr8:1771614-1771624 chr8:1771949-1771962 chr8:1771951-1771960 chr8:1771562-1771572 chr8:1771950-1771960 chr8:1771951-1771961 chr8:1771950-1771961 chr8:1771950-1771961 chr8:1771951-1771961 chr8:1771891-1771901 chr8:1771950-1771961 chr8:1771640-1771650
33	MAFK	chr8:1770995-1771482	K562	blood:	n/a	chr8:1771171-1771186 chr8:1771170-1771184 chr8:1771171-1771187 chr8:1771171-1771182 chr8:1771171-1771182
34	MAX	chr8:1771135-1772276	A549	lung:	n/a	chr8:1771949-1771962 chr8:1771950-1771960 chr8:1771614-1771624 chr8:1771949-1771962 chr8:1771951-1771960 chr8:1771562-1771572 chr8:1771950-1771960 chr8:1771951-1771961 chr8:1771950-1771961 chr8:1771950-1771961 chr8:1771951-1771961 chr8:1771891-1771901 chr8:1771950-1771961 chr8:1771640-1771650
35	MXI1	chr8:1770991-1772730	SK-N-SH	brain:	n/a	chr8:1771950-1771959 chr8:1771952-1771961 chr8:1771950-1771959 chr8:1771952-1771961
36	MAX	chr8:1771190-1772278	HCT-116	colon:	n/a	chr8:1771949-1771962 chr8:1771950-1771960 chr8:1771614-1771624 chr8:1771949-1771962 chr8:1771951-1771960 chr8:1771562-1771572 chr8:1771950-1771960 chr8:1771951-1771961 chr8:1771950-1771961 chr8:1771950-1771961 chr8:1771951-1771961 chr8:1771891-1771901 chr8:1771950-1771961 chr8:1771640-1771650
37	MAFK	chr8:1770831-1771508	Hela-S3	cervix:	n/a	chr8:1771171-1771186 chr8:1771170-1771184 chr8:1771171-1771187 chr8:1771171-1771182 chr8:1771171-1771182
38	E2F6	chr8:1771152-1772281	H1-hESC	embryonic stem cell:	n/a	chr8:1771938-1771947 chr8:1771867-1771879 chr8:1771784-1771796 chr8:1771886-1771895 chr8:1771784-1771793
39	FOS	chr8:1771078-1771499	MCF10A-Er-Src	breast:	n/a	chr8:1771481-1771495
40	MAX	chr8:1771223-1772167	Hela-S3	cervix:	n/a	chr8:1771949-1771962 chr8:1771950-1771960 chr8:1771614-1771624 chr8:1771949-1771962 chr8:1771951-1771960 chr8:1771562-1771572 chr8:1771950-1771960 chr8:1771951-1771961 chr8:1771950-1771961 chr8:1771950-1771961 chr8:1771951-1771961 chr8:1771891-1771901 chr8:1771950-1771961 chr8:1771640-1771650
41	FOS	chr8:1771234-1771490	HUVEC	blood vessel:	n/a	n/a
42	E2F4	chr8:1771170-1772176	MCF10A-Er-Src	breast:	n/a	chr8:1771938-1771947 chr8:1771867-1771879 chr8:1771784-1771796 chr8:1771886-1771895 chr8:1771784-1771793
43	MAFK	chr8:1771026-1771323	HepG2	liver:	n/a	chr8:1771171-1771186 chr8:1771170-1771184 chr8:1771171-1771187 chr8:1771171-1771182 chr8:1771171-1771182
44	FOS	chr8:1771190-1771508	MCF10A-Er-Src	breast:	n/a	chr8:1771481-1771495
45	MAX	chr8:1771223-1771644	MCF-7	breast:	n/a	chr8:1771614-1771624 chr8:1771562-1771572
46	TCF12	chr8:1771221-1772148	A549	lung:	n/a	chr8:1771505-1771515 chr8:1771507-1771514 chr8:1771465-1771475 chr8:1771469-1771476
47	MAX	chr8:1771097-1772384	A549	lung:	n/a	chr8:1771949-1771962 chr8:1771950-1771960 chr8:1771614-1771624 chr8:1771949-1771962 chr8:1771951-1771960 chr8:1771562-1771572 chr8:1771950-1771960 chr8:1771951-1771961 chr8:1771950-1771961 chr8:1771950-1771961 chr8:1771951-1771961 chr8:1771891-1771901 chr8:1771950-1771961 chr8:1771640-1771650
48	E2F6	chr8:1771132-1772286	A549	lung:	n/a	chr8:1771938-1771947 chr8:1771867-1771879 chr8:1771784-1771796 chr8:1771886-1771895 chr8:1771784-1771793
49	TCF12	chr8:1771222-1772329	ECC-1	luminal epithelium:	n/a	chr8:1771505-1771515 chr8:1771507-1771514 chr8:1771465-1771475 chr8:1771469-1771476

No.	Distal block	Cell Line	Cell type
1	chr8:1708451..1710291-chr8:1769924..1772142,2	K562	blood:
2	chr8:1709347..1712341-chr8:1770235..1771752,2	MCF-7	breast:
3	chr8:1764550..1766629-chr8:1770415..1772487,2	K562	blood:
4	chr8:1769937..1771639-chr8:1774044..1776450,2	MCF-7	breast:
5	chr8:1770355..1772056-chr8:1783670..1785482,2	MCF-7	breast:

Variant related genes	Relation type
ARHGEF10	TF binding region
ENSG00000104728	Chromatin interaction
ENSG00000182372	Chromatin interaction
ENSG00000207826	Chromatin interaction
ENSG00000253982	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:36 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv889697	chr8:1238564-1861971	Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv889704	chr8:1563904-1965389	Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Active TSS 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 miRNA target site	18 gene(s)	inside rSNPs	diseases
3	nsv889707	chr8:1581839-1920461	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv889708	chr8:1581839-1965389	Genic enhancers Strong transcription Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv889709	chr8:1581839-1965389	Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS 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	17 gene(s)	inside rSNPs	diseases
6	nsv889711	chr8:1591412-1904157	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Strong transcription 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	14 gene(s)	inside rSNPs	diseases
7	nsv889712	chr8:1591412-2337777	Weak transcription Active TSS Strong transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
8	nsv889714	chr8:1616718-1965389	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
9	nsv1034490	chr8:1654716-1782467	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers 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	10 gene(s)	inside rSNPs	diseases
10	nsv532892	chr8:1687433-1839578	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
11	nsv465276	chr8:1701432-1777571	Active TSS Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
12	nsv609530	chr8:1701432-1777571	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
13	nsv609531	chr8:1717036-1965389	Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
14	nsv824454	chr8:1740369-1802873	Genic enhancers Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
15	nsv1025444	chr8:1743663-1864809	Genic enhancers Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS 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	7 gene(s)	inside rSNPs	diseases
16	nsv539299	chr8:1743663-1864809	Active TSS Weak transcription Strong transcription Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
17	nsv470167	chr8:1746949-1886640	Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
18	nsv465277	chr8:1746950-1888447	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS 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	9 gene(s)	inside rSNPs	diseases
19	nsv609533	chr8:1746950-1888447	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
20	nsv889717	chr8:1746950-1924237	Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
21	nsv889718	chr8:1748166-1807756	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
22	nsv1017597	chr8:1748941-1865887	Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
23	nsv889720	chr8:1756800-1811397	Enhancers Bivalent/Poised TSS Strong transcription Weak transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA	7 gene(s)	inside rSNPs	diseases
24	nsv889721	chr8:1756800-1815639	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	7 gene(s)	inside rSNPs	diseases
25	nsv889722	chr8:1756800-1857293	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
26	nsv889723	chr8:1756800-1904157	Enhancers Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
27	nsv889724	chr8:1756800-1965389	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
28	nsv1031464	chr8:1763119-1848596	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
29	nsv889725	chr8:1765371-1816527	Strong transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA	7 gene(s)	inside rSNPs	diseases
30	nsv824455	chr8:1767334-1772637	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
31	nsv889726	chr8:1768004-1798128	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
32	nsv889727	chr8:1768004-1815639	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Bivalent Enhancer Enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
33	nsv889728	chr8:1768004-1850622	Strong transcription Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
34	esv3374295	chr8:1770970-1774918	Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
35	esv3323272	chr8:1771095-1774093	Bivalent Enhancer Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
36	nsv370584	chr8:1771238-1771238	Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1762000-1771400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:1765800-1771400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr8:1766400-1771400	Weak transcription	Left Ventricle	heart
4	chr8:1766400-1771400	Weak transcription	Pancreas	Pancrea
5	chr8:1766600-1771600	Weak transcription	Spleen	Spleen
6	chr8:1767800-1771600	Weak transcription	Gastric	stomach
7	chr8:1768600-1771400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr8:1768600-1771600	Weak transcription	Lung	lung
9	chr8:1768800-1771400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr8:1770400-1771400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr8:1770800-1771400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
12	chr8:1770800-1771400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
13	chr8:1770800-1771400	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
14	chr8:1771000-1771400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
15	chr8:1771000-1771400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
16	chr8:1771000-1771400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
17	chr8:1771000-1771400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
18	chr8:1771000-1771400	Enhancers	Primary T helper cells PMA-I stimulated	--
19	chr8:1771000-1771400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr8:1771000-1771400	Enhancers	Primary T killer memory cells from peripheral blood	blood
21	chr8:1771000-1771400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr8:1771000-1771400	Enhancers	Adipose Nuclei	Adipose
23	chr8:1771000-1771400	Weak transcription	Colon Smooth Muscle	Colon
24	chr8:1771000-1771400	Enhancers	Placenta Amnion	Placenta Amnion
25	chr8:1771000-1771400	Enhancers	Rectal Smooth Muscle	rectum
26	chr8:1771000-1771400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
27	chr8:1771000-1771400	Enhancers	NHLF	lung
28	chr8:1771000-1771400	Enhancers	Osteobl	bone
29	chr8:1771000-1771600	Bivalent Enhancer	Primary B cells from peripheral blood	blood
30	chr8:1771000-1771600	Enhancers	Primary T helper naive cells from peripheral blood	blood
31	chr8:1771000-1771600	Enhancers	Brain Substantia Nigra	brain
32	chr8:1771000-1772600	Active TSS	ES-I3 Cell Line	embryonic stem cell
33	chr8:1771000-1772600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr8:1771000-1772600	Enhancers	Stomach Mucosa	stomach
35	chr8:1771000-1772800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr8:1771000-1772800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr8:1771000-1772800	Active TSS	Fetal Kidney	kidney
38	chr8:1771000-1772800	Active TSS	HMEC	breast
39	chr8:1771000-1774200	Active TSS	Aorta	Aorta
40	chr8:1771200-1771400	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr8:1771200-1771400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr8:1771200-1771400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr8:1771200-1771400	Bivalent Enhancer	Primary hematopoietic stem cells	blood
44	chr8:1771200-1771400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
45	chr8:1771200-1771400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
46	chr8:1771200-1771400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr8:1771200-1771400	Flanking Active TSS	Brain Anterior Caudate	brain
48	chr8:1771200-1771400	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
49	chr8:1771200-1771400	Flanking Active TSS	Fetal Heart	heart
50	chr8:1771200-1771400	Enhancers	Pancreatic Islets	Pancreatic Islet

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