Variant report

Variant	rs55667166
Chromosome Location	chr4:775956-775957
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:349)
CpG islands
(count:61)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:349 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	NR2F2	chr4:775016-776275	K562	blood:	n/a	n/a
2	ZMIZ1	chr4:775940-776216	K562	blood:	n/a	n/a
3	TAF1	chr4:775201-776465	SK-N-SH	brain:	n/a	n/a
4	POLR2A	chr4:775866-776222	A549	lung:	n/a	n/a
5	YY1	chr4:774875-776448	GM12878	blood:	n/a	chr4:775074-775083 chr4:775408-775422 chr4:775078-775100 chr4:775192-775201 chr4:775413-775424
6	MYC	chr4:775887-776296	K562	blood:	n/a	n/a
7	GATA3	chr4:775618-776578	T-47D	breast:	n/a	n/a
8	MYC	chr4:775954-775956	MCF-7	breast:	n/a	n/a
9	NFIC	chr4:775465-776364	HepG2	liver:	n/a	n/a
10	UBTF	chr4:775020-776119	K562	blood:	n/a	n/a
11	MYC	chr4:775106-776294	K562	blood:	n/a	n/a
12	MYC	chr4:775126-776368	K562	blood:	n/a	n/a
13	HMGN3	chr4:774971-776238	K562	blood:	n/a	n/a
14	POLR2A	chr4:774610-776508	Hela-S3	cervix:	n/a	n/a
15	EP300	chr4:775545-776570	T-47D	breast:	n/a	chr4:775742-775751
16	STAT3	chr4:775717-776253	MCF10A-Er-Src	breast:	n/a	chr4:775772-775784 chr4:775895-775906
17	TAF1	chr4:775268-776070	K562	blood:	n/a	n/a
18	POLR2A	chr4:775321-776317	HCT-116	colon:	n/a	n/a
19	HEY1	chr4:775270-776626	HepG2	liver:	n/a	chr4:775795-775810 chr4:775739-775754 chr4:775402-775417
20	STAT1	chr4:775223-776141	GM12878	blood:	n/a	chr4:775772-775784 chr4:775414-775426
21	POLR2A	chr4:775834-776653	HepG2	liver:	n/a	n/a
22	MYBL2	chr4:775273-776553	HepG2	liver:	n/a	n/a
23	POLR2A	chr4:775338-776233	SK-N-MC	brain:	n/a	n/a
24	POLR2A	chr4:775284-776261	K562	blood:	n/a	n/a
25	POLR2A	chr4:775379-776390	GM12878	blood:	n/a	n/a
26	POLR2A	chr4:775305-776330	A549	lung:	n/a	n/a
27	SIN3AK20	chr4:775017-776701	MCF-7	breast:	n/a	n/a
28	PML	chr4:775178-776247	K562	blood:	n/a	n/a
29	YY1	chr4:775231-776260	K562	blood:	n/a	chr4:775408-775422 chr4:775413-775424
30	TCF12	chr4:775126-775965	ECC-1	luminal epithelium:	n/a	n/a
31	MAX	chr4:775370-776483	HepG2	liver:	n/a	n/a
32	RCOR1	chr4:775532-776185	Hela-S3	cervix:	n/a	n/a
33	MAX	chr4:775185-776372	K562	blood:	n/a	n/a
34	POLR2A	chr4:775293-776261	K562	blood:	n/a	n/a
35	POLR2A	chr4:770558-777225	HepG2	liver:	n/a	n/a
36	MAX	chr4:775383-776356	A549	lung:	n/a	n/a
37	TAF1	chr4:775068-776322	HepG2	liver:	n/a	n/a
38	MXI1	chr4:775487-776310	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr4:775405-776233	Hela-S3	cervix:	n/a	n/a
40	BHLHE40	chr4:775249-776374	K562	blood:	n/a	chr4:775406-775422 chr4:775398-775414 chr4:775735-775751
41	POLR2A	chr4:774947-776543	H1-neurons	neurons:	n/a	n/a
42	POLR2A	chr4:775823-776353	U87	brain:	n/a	n/a
43	CREB1	chr4:775249-776454	GM12878	blood:	n/a	n/a
44	POLR2A	chr4:772703-776479	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr4:774729-776399	NB4	blood:	n/a	n/a
46	TBL1XR1	chr4:775435-776161	K562	blood:	n/a	n/a
47	SIN3AK20	chr4:775736-776065	K562	blood:	n/a	n/a
48	SP1	chr4:775427-776504	HepG2	liver:	n/a	chr4:775795-775804 chr4:775768-775782 chr4:775737-775748 chr4:775489-775501 chr4:776077-776086 chr4:775491-775500 chr4:775490-775499 chr4:775491-775500 chr4:775643-775664 chr4:775456-775470 chr4:775489-775501
49	HCFC1	chr4:775183-776352	Hela-S3	cervix:	n/a	n/a
50	CREB1	chr4:775030-776659	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:775927-775977	MCF10A-Er-Src	breast:	n/a
2	chr4:775927-775977	RPTEC	kidney:	n/a
3	chr4:775927-775977	IMR90	lung:	fetal
4	chr4:775927-775977	HEK293	kidney:	embryo
5	chr4:775927-775977	HPAEpiC	pulmonary alveolar:	n/a
6	chr4:775927-775977	ECC-1	luminal epithelium:	n/a
7	chr4:775927-775977	SK-N-MC	brain:	n/a
8	chr4:775927-775977	HIPEpiC	eye:	n/a
9	chr4:775927-775977	AG09319	gingival:	n/a
10	chr4:775927-775977	Hepatocyte	liver:	n/a
11	chr4:775927-775977	BE2_C	brain:	n/a
12	chr4:775927-775977	GM19239	blood:	n/a
13	chr4:775927-775977	A549	lung:	n/a
14	chr4:775927-775977	T-47D	breast:	n/a
15	chr4:775927-775977	HEEpiC	esophagus:	n/a
16	chr4:775927-775977	HCM	heart:	n/a
17	chr4:775927-775977	SKMC	muscle:	n/a
18	chr4:775927-775977	AG04450	lung:	fetal
19	chr4:775927-775977	MCF-7	breast:	n/a
20	chr4:775927-775977	GM12892	blood:	n/a
21	chr4:775927-775977	HCF	heart:	n/a
22	chr4:775927-775977	K562	blood:	n/a
23	chr4:775927-775977	AoSMC	blood vessel:	n/a
24	chr4:775927-775977	PrEC	prostate:	n/a
25	chr4:775927-775977	NT2-D1	testis:	n/a
26	chr4:775927-775977	SAEC	small airway:	n/a
27	chr4:775927-775977	HUVEC	blood vessel:	n/a
28	chr4:775927-775977	PANC-1	pancreas:	n/a
29	chr4:775927-775977	Jurkat	blood:	n/a
30	chr4:775927-775977	NB4	blood:	n/a
31	chr4:775927-775977	H1-hESC	embryonic stem cell:	embryo
32	chr4:775927-775977	PFSK-1	brain:	n/a
33	chr4:775927-775977	CMK	blood:	n/a
34	chr4:775927-775977	AG04449	skin:	fetal
35	chr4:775927-775977	ovcar-3	ovarian:	n/a
36	chr4:775927-775977	SK-N-SH	brain:	n/a
37	chr4:775927-775977	HRPEpiC	eye:	n/a
38	chr4:775927-775977	GM06990	blood:	n/a
39	chr4:775927-775977	NHDF-neo	bronchial:	n/a
40	chr4:775927-775977	HCPEpiC	choroid plexus:	n/a
41	chr4:775927-775977	AG10803	skin:	n/a
42	chr4:775927-775977	HRE	kidney:	n/a
43	chr4:775927-775977	BJ	skin:	n/a
44	chr4:775927-775977	AG09309	skin:	n/a
45	chr4:775927-775977	Caco-2	colon:	n/a
46	chr4:775927-775977	HRCEpiC	kidney:	n/a
47	chr4:775927-775977	Hela-S3	cervix:	n/a
48	chr4:775927-775977	HepG2	liver:	n/a
49	chr4:775927-775977	HL-60	blood:	n/a
50	chr4:775927-775977	U87	brain:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:679737..681440-chr4:774148..776582,2	K562	blood:
2	chr4:735724..738302-chr4:774438..777111,2	MCF-7	breast:
3	chr4:774894..778846-chr4:965454..968160,4	MCF-7	breast:
4	chr4:773572..776391-chr4:979959..982266,2	MCF-7	breast:
5	chr4:671080..676330-chr4:771868..776883,7	K562	blood:
6	chr4:775742..777793-chr4:821294..823838,2	MCF-7	breast:
7	chr4:775576..776177-chr6:27100717..27101262,2	Hela-S3	cervix:
8	chr4:773678..778564-chr4:818343..821273,5	K562	blood:
9	chr4:735917..738355-chr4:773628..776647,3	MCF-7	breast:
10	chr4:774335..777276-chr4:923482..926205,2	K562	blood:
11	chr4:773038..776439-chr4:923639..926176,4	MCF-7	breast:
12	chr4:774443..776550-chr4:1003219..1006058,2	MCF-7	breast:
13	chr4:774284..777559-chr4:817781..820963,6	MCF-7	breast:
14	chr4:758084..763800-chr4:770671..778725,12	MCF-7	breast:
15	chr19:30155987..30156547-chr4:775222..776214,2	NB4	blood:
16	chr4:774518..776312-chr4:2935741..2938166,2	MCF-7	breast:
17	chr4:774211..776951-chr4:981590..984228,3	MCF-7	breast:
18	chr4:666044..670200-chr4:772961..777371,6	K562	blood:

No data

Variant related genes	Relation type
ENSG00000249592	TF binding region
ENSG00000249592	CpG island
ENSG00000166289	Chromatin interaction
ENSG00000169020	Chromatin interaction
ENSG00000249673	Chromatin interaction
ENSG00000185619	Chromatin interaction
ENSG00000109736	Chromatin interaction
ENSG00000127419	Chromatin interaction
ENSG00000196787	Chromatin interaction
ENSG00000233799	Chromatin interaction
ENSG00000127415	Chromatin interaction
ENSG00000127418	Chromatin interaction
ENSG00000178950	Chromatin interaction
ENSG00000168993	Chromatin interaction
ENSG00000145214	Chromatin interaction
ENSG00000215375	Chromatin interaction
ENSG00000169026	Chromatin interaction

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10004297	1.00[ASN][1000 genomes]
rs11930710	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13111051	1.00[ASN][1000 genomes]
rs13145884	1.00[ASN][1000 genomes]
rs28587502	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28638011	1.00[ASN][1000 genomes]
rs3733356	1.00[ASN][1000 genomes]
rs3733357	1.00[ASN][1000 genomes]
rs3816679	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3822027	1.00[ASN][1000 genomes]
rs4234855	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55974756	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56074082	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6811804	1.00[ASN][1000 genomes]
rs6815765	1.00[ASN][1000 genomes]
rs6838243	1.00[ASN][1000 genomes]
rs73207755	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73222805	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73222806	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73222810	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73222827	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73222831	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73222832	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73222841	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73222842	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7655749	1.00[ASN][1000 genomes]
rs7655941	1.00[ASN][1000 genomes]
rs7661962	1.00[ASN][1000 genomes]
rs7662167	1.00[ASN][1000 genomes]
rs7674850	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1011715	chr4:43860-823487	Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
2	nsv1005224	chr4:507005-900281	Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Strong transcription Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
3	nsv536976	chr4:507005-900281	Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS 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 miRNA target site	41 gene(s)	inside rSNPs	diseases
4	nsv822425	chr4:540105-1413799	Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	108 gene(s)	inside rSNPs	diseases
5	esv2757916	chr4:603208-931354	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
6	esv2759217	chr4:603208-931354	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
7	nsv878247	chr4:607202-925149	Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
8	nsv530490	chr4:614355-1399150	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Active TSS 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	104 gene(s)	inside rSNPs	diseases
9	esv1829397	chr4:655939-1041957	Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
10	nsv878254	chr4:708932-899143	Strong transcription Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
11	nsv878255	chr4:708932-1052488	Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
12	nsv878257	chr4:712222-852313	Strong transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
13	nsv878258	chr4:712222-1058358	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
14	nsv878259	chr4:713920-852313	Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
15	nsv878260	chr4:713920-1052488	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
16	nsv818207	chr4:753944-821490	Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Weak 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	29 gene(s)	inside rSNPs	diseases
17	nsv878261	chr4:756686-1047794	Active TSS Genic enhancers 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 target site	43 gene(s)	inside rSNPs	diseases
18	nsv1007928	chr4:757263-813885	Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
19	nsv520136	chr4:759709-780883	ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
20	nsv1003219	chr4:769894-1105464	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
21	nsv515844	chr4:771587-780883	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
22	nsv526780	chr4:771587-786401	Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription 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	23 gene(s)	inside rSNPs	diseases
23	nsv521402	chr4:771587-793763	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
24	nsv878262	chr4:771587-865227	Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
25	nsv878263	chr4:771587-1047794	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:774000-776200	Active TSS	Pancreatic Islets	Pancreatic Islet
2	chr4:774000-776200	Active TSS	NHDF-Ad	bronchial
3	chr4:774200-776000	Active TSS	iPS-18 Cell Line	embryonic stem cell
4	chr4:774200-776000	Active TSS	Pancreas	Pancrea
5	chr4:774200-776200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr4:774200-776200	Active TSS	iPS-15b Cell Line	embryonic stem cell
7	chr4:774200-776200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr4:774200-776400	Active TSS	Gastric	stomach
9	chr4:774400-776000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
10	chr4:774400-776000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr4:774400-776200	Active TSS	Left Ventricle	heart
12	chr4:774400-776400	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr4:774400-776400	Active TSS	Aorta	Aorta
14	chr4:774400-776400	Active TSS	Right Atrium	heart
15	chr4:774400-776400	Active TSS	Right Ventricle	heart
16	chr4:774400-776600	Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr4:774600-776000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr4:774600-776000	Active TSS	HUES6 Cell Line	embryonic stem cell
19	chr4:774600-776000	Active TSS	iPS-20b Cell Line	embryonic stem cell
20	chr4:774600-776000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr4:774600-776000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr4:774600-776000	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr4:774600-776000	Enhancers	Fetal Brain Male	brain
24	chr4:774600-776000	Active TSS	Fetal Intestine Large	intestine
25	chr4:774600-776000	Active TSS	Fetal Lung	lung
26	chr4:774600-776000	Active TSS	Placenta Amnion	Placenta Amnion
27	chr4:774600-776000	Active TSS	HSMM	muscle
28	chr4:774600-776000	Active TSS	NH-A	brain
29	chr4:774600-776200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr4:774600-776200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr4:774600-776200	Active TSS	HUES64 Cell Line	embryonic stem cell
32	chr4:774600-776200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr4:774600-776200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr4:774600-776200	Active TSS	Brain Anterior Caudate	brain
35	chr4:774600-776200	Active TSS	Brain Hippocampus Middle	brain
36	chr4:774600-776200	Active TSS	Fetal Kidney	kidney
37	chr4:774600-776200	Active TSS	Hela-S3	cervix
38	chr4:774600-776200	Active TSS	HSMMtube	muscle
39	chr4:774600-776400	Active TSS	H9 Cell Line	embryonic stem cell
40	chr4:774600-776400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
41	chr4:774600-776600	Active TSS	Ovary	ovary
42	chr4:774800-776000	Active TSS	H1 Cell Line	embryonic stem cell
43	chr4:774800-776000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr4:774800-776000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr4:774800-776000	Active TSS	HUES48 Cell Line	embryonic stem cell
46	chr4:774800-776000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
47	chr4:774800-776000	Active TSS	Breast Myoepithelial Primary Cells	Breast
48	chr4:774800-776000	Active TSS	Primary T helper naive cells from peripheral blood	blood
49	chr4:774800-776000	Active TSS	Primary T helper cells PMA-I stimulated	--
50	chr4:774800-776000	Active TSS	Primary T killer memory cells from peripheral blood	blood

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