Variant report

Variant	rs1790731
Chromosome Location	chr11:67122410-67122411
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	chr11:67120272-67122666	PANC-1	pancreas:	n/a	n/a
2	FOSL2	chr11:67121795-67122527	A549	lung:	n/a	chr11:67122186-67122194 chr11:67122184-67122196
3	STAT3	chr11:67121942-67122442	MCF10A-Er-Src	breast:	n/a	chr11:67122388-67122400 chr11:67122048-67122060 chr11:67122220-67122231
4	RXRA	chr11:67121826-67122528	SK-N-SH	brain:	n/a	chr11:67122154-67122170 chr11:67122156-67122169 chr11:67122156-67122170 chr11:67122156-67122169 chr11:67122156-67122169 chr11:67122152-67122172 chr11:67122155-67122164
5	POLR2A	chr11:67122232-67122547	Gliobla	brain:	n/a	n/a
6	ELF1	chr11:67121866-67122517	K562	blood:	n/a	n/a
7	FOSL2	chr11:67121907-67122471	HepG2	liver:	n/a	chr11:67122186-67122194 chr11:67122184-67122196
8	ELK4	chr11:67122099-67122502	Hela-S3	cervix:	n/a	n/a
9	SP1	chr11:67120157-67122773	A549	lung:	n/a	chr11:67121108-67121117 chr11:67120700-67120712 chr11:67121152-67121162 chr11:67121106-67121118 chr11:67121106-67121117 chr11:67121049-67121058 chr11:67121151-67121163 chr11:67120309-67120318 chr11:67121641-67121650 chr11:67120590-67120604 chr11:67121108-67121117 chr11:67121152-67121162 chr11:67121201-67121210 chr11:67121151-67121163 chr11:67120309-67120319 chr11:67121083-67121104 chr11:67121240-67121261 chr11:67121181-67121195 chr11:67120439-67120448 chr11:67121200-67121209 chr11:67120300-67120313 chr11:67121148-67121162 chr11:67121152-67121161 chr11:67121153-67121162 chr11:67121412-67121421 chr11:67121107-67121116 chr11:67121153-67121162 chr11:67121106-67121118 chr11:67121048-67121058
10	SIN3AK20	chr11:67121470-67122802	A549	lung:	n/a	n/a
11	EP300	chr11:67120786-67122516	K562	blood:	n/a	chr11:67121302-67121316
12	YY1	chr11:67122045-67122464	K562	blood:	n/a	n/a
13	SIN3AK20	chr11:67121783-67122661	A549	lung:	n/a	n/a
14	TCF12	chr11:67120040-67123036	A549	lung:	n/a	chr11:67120092-67120102
15	FOXP2	chr11:67122006-67122539	PFSK-1	brain:	n/a	n/a
16	POLR2A	chr11:67121895-67122508	HepG2	liver:	n/a	n/a
17	ATF3	chr11:67121829-67122465	A549	lung:	n/a	n/a
18	MAZ	chr11:67121934-67122519	Hela-S3	cervix:	n/a	n/a
19	POLR2A	chr11:67121790-67122556	K562	blood:	n/a	n/a
20	SP1	chr11:67121852-67122445	HepG2	liver:	n/a	n/a
21	HEY1	chr11:67121897-67122449	K562	blood:	n/a	n/a
22	POLR2A	chr11:67121898-67123602	A549	lung:	n/a	n/a
23	SRF	chr11:67122037-67122420	K562	blood:	n/a	chr11:67122205-67122215
24	MYC	chr11:67121687-67122647	K562	blood:	n/a	chr11:67121821-67121831
25	ELF1	chr11:67121870-67123047	A549	lung:	n/a	n/a
26	ETS1	chr11:67121727-67122635	A549	lung:	n/a	chr11:67122214-67122228 chr11:67122216-67122227
27	POLR2A	chr11:67120476-67122740	A549	lung:	n/a	n/a
28	MTA3	chr11:67121117-67122438	GM12878	blood:	n/a	n/a
29	ZBTB33	chr11:67121956-67122419	A549	lung:	n/a	n/a
30	GABPA	chr11:67121838-67122511	A549	lung:	n/a	n/a
31	BHLHE40	chr11:67122028-67122534	K562	blood:	n/a	n/a
32	NR2F2	chr11:67120755-67122650	K562	blood:	n/a	chr11:67122152-67122167
33	TEAD4	chr11:67121743-67122486	HepG2	liver:	n/a	n/a
34	SRF	chr11:67122165-67122444	HepG2	liver:	n/a	chr11:67122205-67122215
35	TAF1	chr11:67122076-67122462	K562	blood:	n/a	n/a
36	CREB1	chr11:67121913-67122491	A549	lung:	n/a	n/a
37	ETS1	chr11:67122063-67122413	K562	blood:	n/a	chr11:67122214-67122228 chr11:67122216-67122227
38	SRF	chr11:67121985-67122618	ECC-1	luminal epithelium:	n/a	chr11:67122205-67122215
39	JUND	chr11:67121843-67122916	A549	lung:	n/a	chr11:67122186-67122194 chr11:67122184-67122195 chr11:67122184-67122196
40	FOSL2	chr11:67121908-67122483	MCF-7	breast:	n/a	chr11:67122186-67122194 chr11:67122184-67122196
41	POLR2A	chr11:67119867-67122495	Raji	blood:	n/a	n/a
42	TAF1	chr11:67121919-67122568	A549	lung:	n/a	n/a
43	POLR2A	chr11:67119963-67123806	U87	brain:	n/a	n/a
44	POLR2A	chr11:67121826-67122526	K562	blood:	n/a	n/a
45	TCF12	chr11:67121831-67122447	A549	lung:	n/a	n/a
46	IRF1	chr11:67121884-67122460	K562	blood:	n/a	n/a
47	TAF1	chr11:67122021-67122445	PFSK-1	brain:	n/a	n/a
48	MYBL2	chr11:67121645-67122633	HepG2	liver:	n/a	n/a
49	MXI1	chr11:67121934-67122540	HepG2	liver:	n/a	n/a
50	FOS	chr11:67121728-67122484	HUVEC	blood vessel:	n/a	chr11:67122186-67122194 chr11:67122184-67122196 chr11:67122184-67122195

No.	Distal block	Cell Line	Cell type
1	chr11:67116951..67127260-chr11:67135118..67146037,42	K562	blood:
2	chr11:67119569..67122629-chr11:67231645..67234377,4	MCF-7	breast:
3	chr11:67112769..67115040-chr11:67121657..67123708,3	K562	blood:
4	chr11:67119765..67126816-chr11:67129168..67134805,10	K562	blood:
5	chr11:67069948..67073118-chr11:67121673..67124639,3	MCF-7	breast:
6	chr11:67121023..67122771-chr11:67229925..67232799,2	K562	blood:
7	chr11:67118066..67122624-chr11:67272137..67276691,11	MCF-7	breast:
8	chr11:67054960..67058476-chr11:67120507..67123269,5	MCF-7	breast:
9	chr11:67121864..67124508-chr11:67250272..67251792,2	K562	blood:
10	chr11:67029982..67035321-chr11:67120482..67125805,6	K562	blood:
11	chr11:67040558..67045868-chr11:67119770..67124610,5	K562	blood:
12	chr11:67035184..67037391-chr11:67122258..67124075,2	MCF-7	breast:
13	chr11:67032309..67036659-chr11:67119174..67122793,5	MCF-7	breast:
14	chr11:67121181..67122742-chr11:67122996..67124944,2	K562	blood:
15	chr11:67119767..67122418-chr11:67248932..67250571,2	MCF-7	breast:
16	chr11:67119033..67122416-chr11:67186034..67189246,4	K562	blood:
17	chr11:67116454..67122701-chr11:67156914..67162562,7	K562	blood:
18	chr11:67120932..67122910-chr2:122287266..122290236,2	MCF-7	breast:
19	chr11:67075683..67087551-chr11:67114391..67125856,27	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAD9A-4	chr11:67121054-67126866	NONHSAT022409

Variant related genes	Relation type
POLD4	TF binding region
ENSG00000167797	Chromatin interaction
ENSG00000172663	Chromatin interaction
ENSG00000110711	Chromatin interaction
ENSG00000201684	Chromatin interaction
ENSG00000175505	Chromatin interaction
ENSG00000172830	Chromatin interaction
ENSG00000265451	Chromatin interaction
ENSG00000175482	Chromatin interaction
ENSG00000074054	Chromatin interaction
ENSG00000172932	Chromatin interaction
ENSG00000173020	Chromatin interaction
ENSG00000172531	Chromatin interaction
ENSG00000110697	Chromatin interaction
ENSG00000172613	Chromatin interaction
ENSG00000172508	Chromatin interaction
ENSG00000264229	Chromatin interaction
ENSG00000256514	Chromatin interaction

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10736657	0.85[ASN][1000 genomes]
rs10896166	0.95[ASN][1000 genomes]
rs11819880	0.83[EUR][1000 genomes]
rs11825943	0.83[EUR][1000 genomes]
rs11827639	0.83[EUR][1000 genomes]
rs12288048	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12785732	0.83[EUR][1000 genomes]
rs12788405	0.96[EUR][1000 genomes]
rs12790040	0.84[ASN][1000 genomes]
rs12791853	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12805811	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1419861	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1558257	0.82[JPT][hapmap]
rs1638569	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17878756	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17883741	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1790735	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1790737	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1790738	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1790739	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1790762	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1894112	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1944096	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2286619	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2298815	0.88[CHB][hapmap];0.82[JPT][hapmap];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2429459	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2429463	0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2511057	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2514257	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2532605	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2852875	0.82[AFR][1000 genomes];0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2852877	0.82[YRI][hapmap]
rs34000912	0.90[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs34087937	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35176549	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35821109	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35876769	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35992831	0.83[EUR][1000 genomes]
rs3737460	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4244822	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61734600	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6591241	0.88[ASN][1000 genomes]
rs66466718	0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs71457775	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7394531	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7934433	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs867193	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9326373	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9734588	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531397	chr11:66653381-67465721	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
2	nsv933183	chr11:67008447-67160993	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
3	nsv897796	chr11:67021518-67186000	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
4	nsv897797	chr11:67023040-67293234	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers 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 miRNA target site	206 gene(s)	inside rSNPs	diseases
5	nsv1043037	chr11:67027193-67357425	Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
6	nsv468603	chr11:67033076-67164495	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
7	nsv555253	chr11:67033076-67164495	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
8	nsv897801	chr11:67033076-67432479	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	236 gene(s)	inside rSNPs	diseases
9	nsv1047890	chr11:67058231-67184436	Flanking Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
10	nsv1048230	chr11:67058231-67252397	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	146 gene(s)	inside rSNPs	diseases
11	nsv897804	chr11:67090571-67224278	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67120800-67124200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr11:67121000-67122600	Weak transcription	Small Intestine	intestine
3	chr11:67121000-67126000	Enhancers	Spleen	Spleen
4	chr11:67121200-67122600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
5	chr11:67121200-67122800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
6	chr11:67121200-67122800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
7	chr11:67121200-67123000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
8	chr11:67121200-67125000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr11:67121200-67125000	Enhancers	Lung	lung
10	chr11:67121200-67125000	Enhancers	Sigmoid Colon	Sigmoid Colon
11	chr11:67121400-67122600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr11:67121400-67122600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr11:67121400-67122600	Flanking Active TSS	NHLF	lung
14	chr11:67121400-67122800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
15	chr11:67121400-67122800	Flanking Active TSS	Stomach Smooth Muscle	stomach
16	chr11:67121400-67122800	Flanking Active TSS	Osteobl	bone
17	chr11:67121400-67123000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
18	chr11:67121400-67123400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr11:67121400-67125400	Flanking Active TSS	Hela-S3	cervix
20	chr11:67121600-67122600	Enhancers	Primary T cells from cord blood	blood
21	chr11:67121600-67122600	Enhancers	Primary hematopoietic stem cells	blood
22	chr11:67121600-67122600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
23	chr11:67121600-67122800	Enhancers	Primary T helper cells fromperipheralblood	blood
24	chr11:67121600-67122800	Enhancers	Primary T killer memory cells from peripheral blood	blood
25	chr11:67121600-67122800	Enhancers	Fetal Lung	lung
26	chr11:67121600-67122800	Flanking Active TSS	K562	blood
27	chr11:67121600-67123000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr11:67121600-67123000	Flanking Active TSS	Duodenum Mucosa	Duodenum
29	chr11:67121600-67123000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr11:67121600-67123000	Flanking Active TSS	Rectal Smooth Muscle	rectum
31	chr11:67121600-67123400	Enhancers	Brain Substantia Nigra	brain
32	chr11:67121600-67123400	Enhancers	Placenta Amnion	Placenta Amnion
33	chr11:67121600-67124000	Enhancers	Fetal Thymus	thymus
34	chr11:67121600-67124400	Flanking Active TSS	HepG2	liver
35	chr11:67121600-67125000	Enhancers	Primary T cells fromperipheralblood	blood
36	chr11:67121600-67125000	Enhancers	Gastric	stomach
37	chr11:67121600-67125200	Flanking Active TSS	A549	lung
38	chr11:67121600-67125800	Enhancers	Fetal Muscle Trunk	muscle
39	chr11:67121600-67126200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
40	chr11:67121600-67126400	Enhancers	Placenta	Placenta
41	chr11:67121600-67132600	Weak transcription	Fetal Brain Female	brain
42	chr11:67121800-67122600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr11:67121800-67122600	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr11:67121800-67122600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
45	chr11:67121800-67122600	Enhancers	Brain Angular Gyrus	brain
46	chr11:67121800-67122800	Enhancers	H1 Cell Line	embryonic stem cell
47	chr11:67121800-67122800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr11:67121800-67122800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
49	chr11:67121800-67123000	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr11:67121800-67123000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood

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