Variant report

Variant	rs4697705
Chromosome Location	chr4:10108127-10108128
allele	A/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	POLR2A	chr4:10108045-10108689	HUVEC	blood vessel:	n/a	n/a
2	FOS	chr4:10108123-10108622	MCF10A-Er-Src	breast:	n/a	chr4:10108337-10108348
3	EP300	chr4:10107909-10108757	SK-N-SH	brain:	n/a	chr4:10108459-10108475
4	GATA2	chr4:10108003-10108692	HUVEC	blood vessel:	n/a	n/a
5	USF2	chr4:10108123-10108131	H1-hESC	embryonic stem cell:	n/a	n/a
6	POLR2A	chr4:10107878-10111552	HUVEC	blood vessel:	n/a	n/a
7	POLR2A	chr4:10107988-10108182	H1-hESC	embryonic stem cell:	n/a	n/a
8	STAT3	chr4:10108123-10108551	MCF10A-Er-Src	breast:	n/a	chr4:10108270-10108278
9	MAX	chr4:10108050-10108748	SK-N-SH	brain:	n/a	chr4:10108504-10108523 chr4:10108507-10108516 chr4:10108592-10108602
10	GATA3	chr4:10107995-10108834	A549	lung:	n/a	n/a
11	POLR2A	chr4:10107812-10120993	GM18505	blood:	n/a	n/a
12	CHD2	chr4:10108109-10108694	Hela-S3	cervix:	n/a	n/a
13	JUND	chr4:10107955-10108733	SK-N-SH	brain:	n/a	chr4:10107995-10108004 chr4:10108337-10108348
14	MAZ	chr4:10107856-10109623	IMR90	lung:	n/a	chr4:10108504-10108523 chr4:10108507-10108516 chr4:10108592-10108602
15	POLR2A	chr4:10107724-10118160	H1-hESC	embryonic stem cell:	n/a	n/a
16	MYC	chr4:10108000-10108653	HUVEC	blood vessel:	n/a	chr4:10108504-10108523 chr4:10108507-10108516 chr4:10108592-10108602
17	POLR2A	chr4:10107942-10108698	HUVEC	blood vessel:	n/a	n/a
18	MXI1	chr4:10107752-10109305	IMR90	lung:	n/a	n/a
19	SIN3AK20	chr4:10108031-10108858	MCF-7	breast:	n/a	n/a
20	POLR2A	chr4:10107881-10108618	K562	blood:	n/a	n/a
21	GATA3	chr4:10107848-10108721	SK-N-SH	brain:	n/a	n/a
22	RXRA	chr4:10108074-10108758	SK-N-SH	brain:	n/a	n/a
23	POLR2A	chr4:10107804-10108638	U87	brain:	n/a	n/a
24	POLR2A	chr4:10105830-10118085	GM12878	blood:	n/a	n/a
25	STAT3	chr4:10108095-10108530	MCF10A-Er-Src	breast:	n/a	chr4:10108270-10108278
26	POLR2A	chr4:10107876-10114115	H1-neurons	neurons:	n/a	n/a
27	POLR2A	chr4:10107960-10108658	SK-N-SH	brain:	n/a	n/a
28	JUN	chr4:10107940-10108586	Hela-S3	cervix:	n/a	chr4:10107995-10108004
29	POLR2A	chr4:10107412-10108779	K562	blood:	n/a	n/a
30	POLR2A	chr4:10107901-10108198	H1-hESC	embryonic stem cell:	n/a	n/a
31	SRF	chr4:10107786-10108739	HCT-116	colon:	n/a	chr4:10108275-10108293
32	STAT3	chr4:10108118-10108563	MCF10A-Er-Src	breast:	n/a	chr4:10108270-10108278
33	MAX	chr4:10107989-10108946	HCT-116	colon:	n/a	chr4:10108504-10108523 chr4:10108507-10108516 chr4:10108592-10108602
34	RCOR1	chr4:10108081-10108674	Hela-S3	cervix:	n/a	n/a
35	NFIC	chr4:10107936-10109140	SK-N-SH	brain:	n/a	n/a
36	MAX	chr4:10108000-10108713	Hela-S3	cervix:	n/a	chr4:10108504-10108523 chr4:10108507-10108516 chr4:10108592-10108602
37	POLR2A	chr4:10107811-10108187	GM12892	blood:	n/a	n/a
38	JUND	chr4:10107982-10108799	SK-N-SH	brain:	n/a	chr4:10107995-10108004 chr4:10108337-10108348
39	MAZ	chr4:10108095-10108614	Hela-S3	cervix:	n/a	chr4:10108504-10108523 chr4:10108507-10108516 chr4:10108592-10108602
40	POLR2A	chr4:10107778-10120550	GM12892	blood:	n/a	n/a
41	GATA3	chr4:10107960-10108771	SK-N-SH	brain:	n/a	n/a
42	POLR2A	chr4:10107943-10108779	Hela-S3	cervix:	n/a	n/a
43	POLR2A	chr4:10106170-10121623	GM12878	blood:	n/a	n/a
44	TFAP2C	chr4:10107995-10108614	Hela-S3	cervix:	n/a	n/a
45	FOSL2	chr4:10108041-10108624	SK-N-SH	brain:	n/a	n/a
46	FOSL1	chr4:10107932-10108928	HCT-116	colon:	n/a	chr4:10107995-10108004 chr4:10108426-10108437
47	POLR2A	chr4:10107772-10108692	GM12891	blood:	n/a	n/a
48	POLR2A	chr4:10106984-10117107	K562	blood:	n/a	n/a
49	JUND	chr4:10107913-10108856	HCT-116	colon:	n/a	chr4:10107995-10108004 chr4:10108337-10108348
50	POLR2A	chr4:10107221-10113421	HUVEC	blood vessel:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:10095456..10100275-chr4:10105163..10110395,7	MCF-7	breast:
2	chr4:10019361..10022054-chr4:10108000..10110178,2	K562	blood:

Variant related genes	Relation type
WDR1	TF binding region
ENSG00000109667	Chromatin interaction
ENSG00000071127	Chromatin interaction

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11722946	0.83[EUR][1000 genomes]
rs11722989	0.83[EUR][1000 genomes]
rs11723016	0.82[EUR][1000 genomes]
rs11726271	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12509713	0.94[ASN][1000 genomes]
rs12648479	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12648610	0.89[ASN][1000 genomes]
rs2241474	0.85[EUR][1000 genomes]
rs2241483	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2278121	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs3756225	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs3822242	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4444830	0.84[EUR][1000 genomes]
rs55941493	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs717615	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:41 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533218	chr4:9371016-10252290	Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	74 gene(s)	inside rSNPs	diseases
2	nsv530090	chr4:9383695-10165033	Enhancers Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	70 gene(s)	inside rSNPs	diseases
3	nsv1014216	chr4:9713612-10223836	Transcr. at gene 5' and 3' Genic enhancers Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	53 gene(s)	inside rSNPs	diseases
4	nsv878681	chr4:9802853-10397327	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	51 gene(s)	inside rSNPs	diseases
5	nsv997941	chr4:9805223-10493388	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	54 gene(s)	inside rSNPs	diseases
6	nsv1008649	chr4:9805223-10589802	Weak transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
7	nsv1000587	chr4:9805223-10610752	Flanking Active TSS Enhancers Genic enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
8	nsv537022	chr4:9805223-10610752	Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
9	nsv1003454	chr4:9805223-10710990	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
10	nsv537023	chr4:9805223-10710990	Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
11	nsv1004801	chr4:9814720-10674528	Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
12	nsv537024	chr4:9814720-10674528	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer 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 miRNA	57 gene(s)	inside rSNPs	diseases
13	nsv931483	chr4:9814721-10716463	Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Enhancers Weak transcription 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 miRNA	58 gene(s)	inside rSNPs	diseases
14	nsv537026	chr4:9903566-10262258	Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	48 gene(s)	inside rSNPs	diseases
15	nsv1009972	chr4:9903566-10710990	Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
16	nsv537027	chr4:9903566-10710990	Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
17	esv2752052	chr4:9911872-10313111	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	51 gene(s)	inside rSNPs	diseases
18	nsv1010620	chr4:9937123-10686682	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
19	nsv530280	chr4:9947818-10940041	Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	66 gene(s)	inside rSNPs	diseases
20	nsv532706	chr4:9948018-10451450	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
21	nsv1013022	chr4:9961220-10230042	Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
22	nsv537028	chr4:9961220-10230042	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
23	nsv537029	chr4:9961220-10262258	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
24	nsv878691	chr4:9966477-10418078	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
25	nsv1013487	chr4:9972011-10320963	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
26	nsv829857	chr4:9982514-10155835	Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
27	nsv469621	chr4:9987670-10142287	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
28	nsv482719	chr4:9987670-10142287	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
29	nsv1008067	chr4:10004664-10262258	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
30	nsv537030	chr4:10004664-10262258	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
31	nsv869057	chr4:10013411-10875454	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	65 gene(s)	inside rSNPs	diseases
32	nsv537031	chr4:10040713-10262258	Enhancers Strong transcription Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
33	nsv997936	chr4:10040713-11009045	Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Active TSS Strong transcription 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	65 gene(s)	inside rSNPs	diseases
34	nsv428438	chr4:10058226-10273779	Flanking Active TSS Genic enhancers Strong transcription Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
35	nsv537032	chr4:10069805-10262258	Genic enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
36	nsv537033	chr4:10069805-10297561	Enhancers Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	49 gene(s)	inside rSNPs	diseases
37	nsv524687	chr4:10080462-10159103	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
38	nsv1003286	chr4:10082156-10230606	Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
39	esv16807	chr4:10099819-10234566	Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
40	nsv537034	chr4:10103058-10262258	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
41	nsv537035	chr4:10103058-10297561	Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10084400-10114000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr4:10084800-10116600	Genic enhancers	Fetal Muscle Leg	muscle
3	chr4:10090400-10116400	Genic enhancers	Primary T cells fromperipheralblood	blood
4	chr4:10091800-10116800	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr4:10093000-10116800	Genic enhancers	Fetal Thymus	thymus
6	chr4:10093800-10110800	Genic enhancers	Primary T cells from cord blood	blood
7	chr4:10093800-10116000	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr4:10097800-10110600	Enhancers	Fetal Brain Male	brain
9	chr4:10098200-10112200	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr4:10100200-10113600	Genic enhancers	Lung	lung
11	chr4:10101000-10116600	Enhancers	Right Atrium	heart
12	chr4:10101200-10110400	Enhancers	Brain Cingulate Gyrus	brain
13	chr4:10101200-10111400	Enhancers	Brain Angular Gyrus	brain
14	chr4:10101200-10111800	Weak transcription	Fetal Kidney	kidney
15	chr4:10102200-10114000	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr4:10102600-10112200	Enhancers	Brain Substantia Nigra	brain
17	chr4:10103800-10108200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr4:10103800-10110400	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr4:10104200-10111000	Enhancers	Psoas Muscle	Psoas
20	chr4:10104200-10116000	Genic enhancers	HUES6 Cell Line	embryonic stem cell
21	chr4:10104400-10113000	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr4:10104600-10109800	Enhancers	Brain Anterior Caudate	brain
23	chr4:10104600-10111000	Genic enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr4:10104600-10111200	Enhancers	Left Ventricle	heart
25	chr4:10104800-10109000	Weak transcription	Aorta	Aorta
26	chr4:10105200-10110800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
27	chr4:10105200-10112200	Weak transcription	Fetal Lung	lung
28	chr4:10105600-10109400	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr4:10105600-10109800	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr4:10105600-10110200	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr4:10105600-10110200	Enhancers	HSMMtube	muscle
32	chr4:10105600-10111000	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr4:10105800-10108800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr4:10105800-10109000	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
35	chr4:10105800-10110200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
36	chr4:10105800-10112600	Enhancers	Stomach Mucosa	stomach
37	chr4:10105800-10116000	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr4:10106000-10108200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr4:10106000-10109600	Enhancers	Small Intestine	intestine
40	chr4:10106000-10110200	Enhancers	Pancreas	Pancrea
41	chr4:10106000-10114600	Genic enhancers	Sigmoid Colon	Sigmoid Colon
42	chr4:10106000-10116600	Genic enhancers	Fetal Stomach	stomach
43	chr4:10106000-10116800	Genic enhancers	Rectal Mucosa Donor 31	rectum
44	chr4:10106600-10108600	Genic enhancers	Rectal Smooth Muscle	rectum
45	chr4:10106600-10109400	Enhancers	Fetal Brain Female	brain
46	chr4:10106600-10110000	Genic enhancers	Primary hematopoietic stem cells	blood
47	chr4:10106600-10110200	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr4:10106600-10113000	Genic enhancers	Spleen	Spleen
49	chr4:10106600-10114400	Genic enhancers	Primary B cells from peripheral blood	blood
50	chr4:10106800-10108200	Strong transcription	HUES48 Cell Line	embryonic stem cell

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