Variant report

Variant	rs532815331
Chromosome Location	chr10:5709165-5709166
allele	C/G
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	MAX	chr10:5708772-5709254	HUVEC	blood vessel:	n/a	chr10:5708953-5708963 chr10:5709104-5709120 chr10:5709103-5709110 chr10:5708964-5708974
2	MXI1	chr10:5707968-5709249	HepG2	liver:	n/a	n/a
3	MAX	chr10:5707834-5709263	K562	blood:	n/a	chr10:5708953-5708963 chr10:5709104-5709120 chr10:5708049-5708059 chr10:5708348-5708358 chr10:5709103-5709110 chr10:5708964-5708974
4	CREB1	chr10:5708000-5709299	HepG2	liver:	n/a	n/a
5	E2F6	chr10:5707905-5709231	K562	blood:	n/a	chr10:5708642-5708654 chr10:5708426-5708436 chr10:5708336-5708346 chr10:5708455-5708465 chr10:5708335-5708346 chr10:5708337-5708345 chr10:5708338-5708345 chr10:5708337-5708345
6	MAX	chr10:5707768-5709232	ECC-1	luminal epithelium:	n/a	chr10:5708953-5708963 chr10:5709104-5709120 chr10:5708049-5708059 chr10:5708348-5708358 chr10:5709103-5709110 chr10:5708964-5708974
7	POLR2A	chr10:5707357-5709256	Raji	blood:	n/a	n/a
8	MAX	chr10:5707631-5709274	NB4	blood:	n/a	chr10:5708953-5708963 chr10:5709104-5709120 chr10:5708049-5708059 chr10:5708348-5708358 chr10:5709103-5709110 chr10:5708964-5708974
9	MYC	chr10:5707540-5709267	A549	lung:	n/a	chr10:5708953-5708963 chr10:5709104-5709120 chr10:5708049-5708059 chr10:5708348-5708358 chr10:5709103-5709110 chr10:5708964-5708974
10	MAX	chr10:5708201-5709273	HepG2	liver:	n/a	chr10:5708953-5708963 chr10:5709104-5709120 chr10:5708348-5708358 chr10:5709103-5709110 chr10:5708964-5708974
11	MAX	chr10:5707695-5709306	HCT-116	colon:	n/a	chr10:5708953-5708963 chr10:5709104-5709120 chr10:5708049-5708059 chr10:5708348-5708358 chr10:5709103-5709110 chr10:5708964-5708974
12	BHLHE40	chr10:5708587-5709192	K562	blood:	n/a	n/a
13	FOXA1	chr10:5708471-5709207	T-47D	breast:	n/a	n/a
14	TCF3	chr10:5708736-5709205	GM12878	blood:	n/a	n/a
15	BCL3	chr10:5708804-5709189	GM12878	blood:	n/a	n/a
16	NFATC1	chr10:5708768-5709242	GM12878	blood:	n/a	n/a
17	BCL3	chr10:5708858-5709224	GM12878	blood:	n/a	n/a
18	MYC	chr10:5707923-5709196	K562	blood:	n/a	chr10:5708953-5708963 chr10:5709104-5709120 chr10:5708049-5708059 chr10:5708348-5708358 chr10:5709103-5709110 chr10:5708964-5708974
19	TCF7L2	chr10:5707839-5709229	HCT-116	colon:	n/a	n/a
20	MYC	chr10:5707716-5709225	K562	blood:	n/a	chr10:5708953-5708963 chr10:5709104-5709120 chr10:5708049-5708059 chr10:5708348-5708358 chr10:5709103-5709110 chr10:5708964-5708974
21	MAX	chr10:5708827-5709215	K562	blood:	n/a	chr10:5708953-5708963 chr10:5709104-5709120 chr10:5709103-5709110 chr10:5708964-5708974
22	MYBL2	chr10:5708452-5709182	HepG2	liver:	n/a	n/a
23	CREB1	chr10:5708369-5709199	HepG2	liver:	n/a	n/a
24	HDAC2	chr10:5707731-5709242	MCF-7	breast:	n/a	chr10:5707761-5707775 chr10:5707765-5707779 chr10:5707764-5707778 chr10:5707762-5707776
25	BHLHE40	chr10:5708641-5709243	HepG2	liver:	n/a	n/a
26	MAX	chr10:5707756-5709337	HepG2	liver:	n/a	chr10:5708953-5708963 chr10:5709104-5709120 chr10:5708049-5708059 chr10:5708348-5708358 chr10:5709103-5709110 chr10:5708964-5708974
27	MYC	chr10:5707679-5709174	K562	blood:	n/a	chr10:5708953-5708963 chr10:5709104-5709120 chr10:5708049-5708059 chr10:5708348-5708358 chr10:5709103-5709110 chr10:5708964-5708974
28	MAX	chr10:5707644-5709351	A549	lung:	n/a	chr10:5708953-5708963 chr10:5709104-5709120 chr10:5708049-5708059 chr10:5708348-5708358 chr10:5709103-5709110 chr10:5708964-5708974
29	MAX	chr10:5707690-5709355	HepG2	liver:	n/a	chr10:5708953-5708963 chr10:5709104-5709120 chr10:5708049-5708059 chr10:5708348-5708358 chr10:5709103-5709110 chr10:5708964-5708974
30	MAX	chr10:5707727-5709294	MCF-7	breast:	n/a	chr10:5708953-5708963 chr10:5709104-5709120 chr10:5708049-5708059 chr10:5708348-5708358 chr10:5709103-5709110 chr10:5708964-5708974
31	ZNF263	chr10:5707511-5709171	HEK293-T-REx	kidney:	n/a	n/a
32	MAX	chr10:5707813-5709199	ECC-1	luminal epithelium:	n/a	chr10:5708953-5708963 chr10:5709104-5709120 chr10:5708049-5708059 chr10:5708348-5708358 chr10:5709103-5709110 chr10:5708964-5708974
33	MAX	chr10:5708405-5709228	H1-hESC	embryonic stem cell:	n/a	chr10:5708953-5708963 chr10:5709104-5709120 chr10:5709103-5709110 chr10:5708964-5708974

No.	Distal block	Cell Line	Cell type
1	chr10:5659171..5662010-chr10:5707160..5709672,2	MCF-7	breast:
2	chr10:5691710..5696017-chr10:5704918..5709884,5	K562	blood:
3	chr10:5706894..5712025-chr10:5724987..5728504,7	MCF-7	breast:
4	chr10:5707719..5709670-chr10:5755550..5758097,2	MCF-7	breast:
5	chr10:5539704..5542101-chr10:5707355..5709721,2	MCF-7	breast:
6	chr10:5708731..5711725-chr10:5733293..5735227,2	MCF-7	breast:
7	chr10:5707157..5710880-chr10:5853405..5856185,3	K562	blood:
8	chr10:5691219..5693694-chr10:5706407..5709884,5	K562	blood:
9	chr10:5486439..5489849-chr10:5706503..5709188,4	MCF-7	breast:
10	chr10:5707879..5710257-chr22:29195153..29198012,2	MCF-7	breast:
11	chr10:5704788..5710194-chr10:5724908..5728833,8	K562	blood:
12	chr10:5706900..5709374-chr10:5740250..5741979,2	MCF-7	breast:
13	chr10:5708441..5709982-chr10:5853880..5856185,2	K562	blood:
14	chr10:5682936..5684955-chr10:5707223..5709652,2	MCF-7	breast:
15	chr10:5487870..5492604-chr10:5704699..5710397,11	MCF-7	breast:
16	chr10:5707177..5709381-chr10:5931479..5933432,3	MCF-7	breast:

Variant related genes	Relation type
ASB13	TF binding region
ENSG00000226647	Chromatin interaction
ENSG00000226471	Chromatin interaction
ENSG00000100219	Chromatin interaction
ENSG00000108021	Chromatin interaction
ENSG00000134452	Chromatin interaction
ENSG00000057608	Chromatin interaction
ENSG00000228951	Chromatin interaction
ENSG00000134461	Chromatin interaction
ENSG00000272764	Chromatin interaction
ENSG00000196372	Chromatin interaction
ENSG00000173848	Chromatin interaction
ENSG00000178372	Chromatin interaction

Extended variants
information (count: 42 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:42 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534685	chr10:4914018-5853324	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers 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 target site	68 gene(s)	inside rSNPs	diseases
2	nsv523491	chr10:5542109-5720067	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
3	esv2757364	chr10:5557024-5720512	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
4	esv2759729	chr10:5557024-5804780	Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
5	esv2758209	chr10:5637111-5804780	Weak transcription Enhancers Flanking Active TSS Strong 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	24 gene(s)	inside rSNPs	diseases
6	nsv519582	chr10:5646103-5720067	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
7	nsv8599	chr10:5649129-5719928	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer 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	23 gene(s)	inside rSNPs	diseases
8	nsv1050965	chr10:5649760-5717125	Enhancers Genic enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
9	nsv1044330	chr10:5652006-5717125	Weak transcription Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription 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	22 gene(s)	inside rSNPs	diseases
10	nsv975791	chr10:5652225-5711077	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
11	nsv466720	chr10:5652277-5715401	Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
12	nsv549892	chr10:5652277-5715401	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS Bivalent Enhancer 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	22 gene(s)	inside rSNPs	diseases
13	nsv1037709	chr10:5652739-5717125	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer 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	22 gene(s)	inside rSNPs	diseases
14	nsv470917	chr10:5654167-5715401	Strong transcription Active TSS Flanking Active TSS Weak transcription Enhancers Genic enhancers Bivalent Enhancer 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	22 gene(s)	inside rSNPs	diseases
15	nsv818742	chr10:5654167-5715401	Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
16	nsv1036492	chr10:5656962-5711147	Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
17	nsv540473	chr10:5656962-5711147	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer 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	22 gene(s)	inside rSNPs	diseases
18	nsv1036253	chr10:5657162-5711008	Strong transcription Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
19	nsv540474	chr10:5657162-5711008	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
20	nsv1040422	chr10:5665458-5714630	Active TSS Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer 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	20 gene(s)	inside rSNPs	diseases
21	nsv1043251	chr10:5665458-5716555	Enhancers Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
22	nsv1052519	chr10:5665458-5717125	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
23	nsv1038690	chr10:5665458-5720424	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
24	nsv1039650	chr10:5665458-5720512	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
25	nsv1041684	chr10:5665458-5722299	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
26	esv2760149	chr10:5665458-5724382	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
27	nsv1054909	chr10:5665458-5724382	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
28	nsv1049620	chr10:5665458-5725208	Bivalent/Poised TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
29	nsv442170	chr10:5665462-5717127	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
30	esv2753700	chr10:5665774-5716555	Enhancers Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS 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	20 gene(s)	inside rSNPs	diseases
31	esv34623	chr10:5665774-5716858	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer 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	20 gene(s)	inside rSNPs	diseases
32	esv35082	chr10:5665774-5716858	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
33	esv2754101	chr10:5665774-5716858	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
34	esv2755272	chr10:5665774-5716858	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
35	nsv1038750	chr10:5668208-5711008	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
36	nsv540475	chr10:5668208-5711008	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Enhancers Genic 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	20 gene(s)	inside rSNPs	diseases
37	nsv894808	chr10:5685301-5712087	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
38	nsv894809	chr10:5696482-5711220	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
39	nsv466721	chr10:5701761-5721653	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
40	nsv549893	chr10:5701761-5721653	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
41	esv3375619	chr10:5706746-5711044	Enhancers Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
42	nsv549894	chr10:5708801-5721653	Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5707400-5709200	Active TSS	Fetal Stomach	stomach
2	chr10:5707400-5709400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr10:5707600-5709200	Active TSS	HSMMtube	muscle
4	chr10:5707800-5709200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr10:5708600-5709200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr10:5708600-5709200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
7	chr10:5708600-5709200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
8	chr10:5708600-5709200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
9	chr10:5708600-5709200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
10	chr10:5708600-5709200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
11	chr10:5708600-5709200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr10:5708600-5709200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr10:5708600-5709200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr10:5708600-5709200	Flanking Active TSS	Adipose Nuclei	Adipose
15	chr10:5708600-5709200	Flanking Active TSS	Liver	Liver
16	chr10:5708600-5709200	Flanking Active TSS	Gastric	stomach
17	chr10:5708600-5709200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
18	chr10:5708600-5709200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
19	chr10:5708600-5709200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
20	chr10:5708600-5709200	Flanking Bivalent TSS/Enh	GM12878-XiMat	blood
21	chr10:5708600-5709200	Flanking Active TSS	HMEC	breast
22	chr10:5708600-5709200	Flanking Active TSS	NH-A	brain
23	chr10:5708600-5709400	Flanking Bivalent TSS/Enh	Dnd41	blood
24	chr10:5708600-5709600	Flanking Active TSS	HepG2	liver
25	chr10:5708600-5709600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
26	chr10:5708600-5709800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr10:5708800-5709200	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
28	chr10:5708800-5709200	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr10:5708800-5709200	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr10:5708800-5709200	Flanking Active TSS	H9 Cell Line	embryonic stem cell
31	chr10:5708800-5709200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr10:5708800-5709200	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
33	chr10:5708800-5709200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
34	chr10:5708800-5709200	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
35	chr10:5708800-5709200	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr10:5708800-5709200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
37	chr10:5708800-5709200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
38	chr10:5708800-5709200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr10:5708800-5709200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
40	chr10:5708800-5709200	Flanking Active TSS	Primary B cells from peripheral blood	blood
41	chr10:5708800-5709200	Flanking Active TSS	Primary T cells from cord blood	blood
42	chr10:5708800-5709200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
43	chr10:5708800-5709200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
44	chr10:5708800-5709200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
45	chr10:5708800-5709200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
46	chr10:5708800-5709200	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr10:5708800-5709200	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
48	chr10:5708800-5709200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
49	chr10:5708800-5709200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr10:5708800-5709200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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