Variant report

Variant	rs11931513
Chromosome Location	chr4:1303290-1303291
allele	G/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	ATF3	chr4:1303046-1303311	K562	blood:	n/a	n/a
2	NFYB	chr4:1303152-1303485	K562	blood:	n/a	n/a
3	USF1	chr4:1303012-1303340	HepG2	liver:	n/a	chr4:1303183-1303192 chr4:1303182-1303193 chr4:1303184-1303193 chr4:1303274-1303290 chr4:1303184-1303193
4	MAX	chr4:1303006-1303336	K562	blood:	n/a	chr4:1303183-1303194 chr4:1303183-1303194 chr4:1303184-1303193
5	USF1	chr4:1302943-1303453	K562	blood:	n/a	chr4:1303183-1303192 chr4:1303182-1303193 chr4:1303184-1303193 chr4:1303274-1303290 chr4:1303184-1303193
6	BACH1	chr4:1303047-1303600	H1-hESC	embryonic stem cell:	n/a	n/a
7	MAZ	chr4:1302815-1304116	IMR90	lung:	n/a	chr4:1303183-1303194 chr4:1303183-1303194 chr4:1303184-1303193
8	GABPA	chr4:1302956-1303386	K562	blood:	n/a	n/a
9	RCOR1	chr4:1303142-1303475	K562	blood:	n/a	n/a
10	NFYB	chr4:1303155-1303449	GM12878	blood:	n/a	n/a
11	POLR2A	chr4:1302949-1303758	HepG2	liver:	n/a	n/a
12	POLR2A	chr4:1302925-1303426	H1-hESC	embryonic stem cell:	n/a	n/a
13	USF1	chr4:1302917-1303397	ECC-1	luminal epithelium:	n/a	chr4:1303183-1303192 chr4:1303182-1303193 chr4:1303184-1303193 chr4:1303274-1303290 chr4:1303184-1303193
14	USF1	chr4:1302914-1303439	H1-hESC	embryonic stem cell:	n/a	chr4:1303183-1303192 chr4:1303182-1303193 chr4:1303184-1303193 chr4:1303274-1303290 chr4:1303184-1303193
15	USF1	chr4:1302952-1303492	K562	blood:	n/a	chr4:1303183-1303192 chr4:1303182-1303193 chr4:1303184-1303193 chr4:1303274-1303290 chr4:1303184-1303193
16	POLR2A	chr4:1302942-1303808	HepG2	liver:	n/a	n/a
17	MXI1	chr4:1303092-1303357	GM12878	blood:	n/a	n/a
18	CHD2	chr4:1303131-1303459	H1-hESC	embryonic stem cell:	n/a	n/a
19	HDAC2	chr4:1303153-1303405	K562	blood:	n/a	n/a
20	MAX	chr4:1302951-1303603	SK-N-SH	brain:	n/a	chr4:1303183-1303194 chr4:1303183-1303194 chr4:1303184-1303193
21	CTCF	chr4:1303160-1303310	AG04449	skin:	n/a	n/a
22	MTA3	chr4:1302859-1303514	GM12878	blood:	n/a	n/a
23	POLR2A	chr4:1302979-1303669	K562	blood:	n/a	n/a
24	CTCF	chr4:1303257-1303452	IMR90	lung:	n/a	n/a
25	MAX	chr4:1302958-1303558	H1-hESC	embryonic stem cell:	n/a	chr4:1303183-1303194 chr4:1303183-1303194 chr4:1303184-1303193
26	TAF1	chr4:1302959-1303302	PFSK-1	brain:	n/a	n/a
27	POLR2A	chr4:1303155-1303328	GM12878	blood:	n/a	n/a
28	POLR2A	chr4:1303044-1303349	HUVEC	blood vessel:	n/a	n/a
29	MXI1	chr4:1302485-1304021	SK-N-SH	brain:	n/a	n/a
30	POLR2A	chr4:1303026-1303809	HepG2	liver:	n/a	n/a
31	ELF1	chr4:1303047-1303388	HepG2	liver:	n/a	n/a
32	EP300	chr4:1303156-1303290	GM12878	blood:	n/a	n/a
33	CHD2	chr4:1303127-1303408	GM12878	blood:	n/a	n/a
34	HEY1	chr4:1302959-1303803	HepG2	liver:	n/a	n/a
35	ZBTB7A	chr4:1303107-1303541	HepG2	liver:	n/a	n/a
36	POLR2A	chr4:1303156-1303473	ProgFib	skin:	n/a	n/a
37	POLR2A	chr4:1302885-1303437	GM12878	blood:	n/a	n/a
38	ELF1	chr4:1303072-1303423	K562	blood:	n/a	n/a
39	USF1	chr4:1302961-1303412	SK-N-SH_RA	brain:	n/a	chr4:1303183-1303192 chr4:1303182-1303193 chr4:1303184-1303193 chr4:1303274-1303290 chr4:1303184-1303193
40	ELF1	chr4:1303062-1303423	K562	blood:	n/a	n/a
41	TBP	chr4:1302987-1303726	H1-hESC	embryonic stem cell:	n/a	n/a
42	RCOR1	chr4:1303262-1303345	GM12878	blood:	n/a	n/a
43	E2F6	chr4:1303065-1303301	K562	blood:	n/a	n/a
44	GABPA	chr4:1302985-1303446	K562	blood:	n/a	chr4:1303390-1303404
45	POLR2A	chr4:1302979-1303862	H1-hESC	embryonic stem cell:	n/a	n/a
46	USF2	chr4:1302835-1303467	H1-hESC	embryonic stem cell:	n/a	chr4:1303183-1303192 chr4:1303184-1303193 chr4:1303274-1303290 chr4:1303184-1303193
47	GABPA	chr4:1303059-1303375	HepG2	liver:	n/a	n/a
48	NRF1	chr4:1303209-1303531	H1-hESC	embryonic stem cell:	n/a	chr4:1303390-1303404
49	CTCF	chr4:1303200-1303350	BJ	skin:	n/a	n/a
50	MAX	chr4:1303011-1303426	GM12878	blood:	n/a	chr4:1303183-1303194 chr4:1303183-1303194 chr4:1303184-1303193

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:1300397..1304694-chr4:1319400..1323043,4	K562	blood:

Variant related genes	Relation type
MAEA	TF binding region
ENSG00000090316	Chromatin interaction

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10013662	1.00[EUR][1000 genomes]
rs11932230	0.81[AMR][1000 genomes]
rs11932895	1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13115935	1.00[EUR][1000 genomes]
rs1383658	1.00[EUR][1000 genomes]
rs1383659	1.00[EUR][1000 genomes]
rs1481168	1.00[EUR][1000 genomes]
rs1680075	0.84[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1680082	0.86[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17164618	1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1732105	0.89[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2127911	1.00[EUR][1000 genomes]
rs34082974	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4336168	1.00[EUR][1000 genomes]
rs4465987	1.00[EUR][1000 genomes]
rs4974567	1.00[EUR][1000 genomes]
rs4974580	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4974581	0.86[YRI][hapmap];0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4974634	1.00[EUR][1000 genomes]
rs4974636	1.00[EUR][1000 genomes]
rs4974641	1.00[EUR][1000 genomes]
rs57461362	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59318613	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59669372	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60410862	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6818213	0.89[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6834402	1.00[EUR][1000 genomes]
rs6835204	1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6851640	0.86[YRI][hapmap]
rs73069991	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73069994	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73071910	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73071925	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73073722	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73073725	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73073727	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73073729	1.00[EUR][1000 genomes]
rs73796061	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7691582	1.00[EUR][1000 genomes]
rs922697	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:31 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	esv3339080	chr4:970630-1546223	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
4	nsv829835	chr4:1097586-1304239	Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
5	nsv878328	chr4:1141573-1990425	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers 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 miRNA miRNA target site	121 gene(s)	inside rSNPs	diseases
6	nsv878330	chr4:1147407-1523930	Strong transcription Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
7	nsv461152	chr4:1159680-1415698	Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
8	nsv593278	chr4:1159680-1415698	Enhancers Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
9	nsv997971	chr4:1191256-1518521	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
10	nsv461155	chr4:1203265-1352685	Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
11	nsv593281	chr4:1203265-1352685	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
12	nsv1002097	chr4:1212573-1320086	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS 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 target site	51 gene(s)	inside rSNPs	diseases
13	nsv536986	chr4:1212573-1320086	Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
14	nsv593298	chr4:1244267-1342521	Flanking Active TSS Strong transcription Genic enhancers Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
15	nsv461156	chr4:1254930-1312394	Strong transcription Flanking Active TSS Genic enhancers Weak transcription Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
16	nsv593299	chr4:1254930-1312394	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
17	nsv593300	chr4:1272664-1312394	Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
18	nsv878338	chr4:1277826-1358449	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
19	nsv878339	chr4:1277826-1363886	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
20	nsv878340	chr4:1277826-1386570	Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
21	nsv878341	chr4:1277826-1391400	Active TSS ZNF genes & repeats Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
22	nsv1002635	chr4:1282603-1402761	Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS 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 target site	37 gene(s)	inside rSNPs	diseases
23	nsv878342	chr4:1291337-1363886	Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
24	nsv878343	chr4:1291337-1391400	Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
25	nsv878344	chr4:1291337-1414684	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
26	nsv878345	chr4:1291337-1563920	Strong transcription Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
27	nsv461157	chr4:1300077-1352685	Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
28	nsv593301	chr4:1300077-1352685	Strong transcription Weak transcription Active TSS Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
29	nsv878346	chr4:1300077-1363886	Genic enhancers Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
30	nsv878347	chr4:1300077-1866358	Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Active TSS Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
31	esv3440400	chr4:1301202-1303700	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 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	chr4:1285200-1303400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:1292000-1303400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr4:1293200-1312000	Weak transcription	Hela-S3	cervix
4	chr4:1293800-1303400	Weak transcription	Aorta	Aorta
5	chr4:1295200-1303400	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr4:1295200-1303400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr4:1299000-1306400	Weak transcription	A549	lung
8	chr4:1301800-1303400	Enhancers	Esophagus	oesophagus
9	chr4:1301800-1305800	Enhancers	Primary T killer memory cells from peripheral blood	blood
10	chr4:1301800-1306000	Genic enhancers	Spleen	Spleen
11	chr4:1302000-1303400	Enhancers	H1 Cell Line	embryonic stem cell
12	chr4:1302200-1303400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr4:1302200-1304000	Enhancers	Sigmoid Colon	Sigmoid Colon
14	chr4:1302200-1305200	Enhancers	Fetal Heart	heart
15	chr4:1302400-1303400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr4:1302400-1303600	Enhancers	Fetal Brain Male	brain
17	chr4:1302400-1304400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
18	chr4:1302400-1304400	Enhancers	Stomach Mucosa	stomach
19	chr4:1302400-1304600	Flanking Active TSS	Stomach Smooth Muscle	stomach
20	chr4:1302400-1305200	Weak transcription	Dnd41	blood
21	chr4:1302600-1303400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr4:1302600-1303400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr4:1302600-1303400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr4:1302600-1303400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr4:1302600-1303400	Flanking Active TSS	Brain Cingulate Gyrus	brain
26	chr4:1302600-1303800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
27	chr4:1302600-1304000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
28	chr4:1302600-1304400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr4:1302600-1304400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr4:1302600-1304400	Flanking Active TSS	Adipose Nuclei	Adipose
31	chr4:1302600-1304800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
32	chr4:1302800-1303400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
33	chr4:1302800-1303400	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr4:1302800-1303600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr4:1302800-1303600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
36	chr4:1302800-1303600	Active TSS	NHLF	lung
37	chr4:1302800-1303800	Flanking Active TSS	Primary B cells from cord blood	blood
38	chr4:1302800-1303800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
39	chr4:1302800-1303800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
40	chr4:1302800-1303800	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr4:1302800-1303800	Active TSS	Ovary	ovary
42	chr4:1302800-1303800	Flanking Active TSS	HUVEC	blood vessel
43	chr4:1302800-1304000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
44	chr4:1302800-1304000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
45	chr4:1302800-1304000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
46	chr4:1302800-1304000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr4:1302800-1304000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr4:1302800-1304000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr4:1302800-1304000	Flanking Active TSS	Liver	Liver
50	chr4:1302800-1304000	Flanking Active TSS	Brain Anterior Caudate	brain

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