Variant report

Variant	rs7943191
Chromosome Location	chr11:62328551-62328552
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	RAD21	chr11:62327890-62328598	MCF-7	breast:	n/a	chr11:62328188-62328207 chr11:62328192-62328202 chr11:62328191-62328204 chr11:62328194-62328203
2	POLR2A	chr11:62327831-62328765	PANC-1	pancreas:	n/a	n/a
3	TCF7L2	chr11:62328179-62328616	PANC-1	pancreas:	n/a	n/a
4	NR2F2	chr11:62327727-62328650	K562	blood:	n/a	n/a
5	POLR2A	chr11:62327962-62328579	HCT-116	colon:	n/a	n/a
6	BRCA1	chr11:62327977-62328618	Hela-S3	cervix:	n/a	n/a
7	POLR2A	chr11:62327469-62328801	PFSK-1	brain:	n/a	n/a
8	MYBL2	chr11:62327917-62328571	HepG2	liver:	n/a	n/a
9	SIN3AK20	chr11:62327917-62328679	PANC-1	pancreas:	n/a	n/a
10	POLR2A	chr11:62328142-62328695	GM12878	blood:	n/a	n/a
11	RXRA	chr11:62327936-62328783	SK-N-SH	brain:	n/a	chr11:62328188-62328208
12	MAZ	chr11:62328019-62328590	Hela-S3	cervix:	n/a	n/a
13	RAD21	chr11:62327845-62328791	SK-N-SH	brain:	n/a	chr11:62328188-62328207 chr11:62328192-62328202 chr11:62328191-62328204 chr11:62328194-62328203
14	GATA3	chr11:62328266-62328651	MCF-7	breast:	n/a	n/a
15	TCF12	chr11:62327885-62328896	SK-N-SH	brain:	n/a	n/a
16	MXI1	chr11:62327925-62328599	Hela-S3	cervix:	n/a	n/a
17	TCF12	chr11:62327951-62328851	SK-N-SH	brain:	n/a	n/a
18	EP300	chr11:62328020-62328631	Hela-S3	cervix:	n/a	n/a
19	POLR2A	chr11:62326857-62328682	GM12892	blood:	n/a	n/a
20	MAX	chr11:62327841-62328642	A549	lung:	n/a	n/a
21	TBP	chr11:62328017-62328567	Hela-S3	cervix:	n/a	n/a
22	ZKSCAN1	chr11:62328009-62328557	Hela-S3	cervix:	n/a	n/a
23	FOSL2	chr11:62327856-62328568	A549	lung:	n/a	chr11:62328156-62328167 chr11:62328269-62328279 chr11:62328276-62328288 chr11:62328278-62328286 chr11:62328269-62328279
24	GATA3	chr11:62327989-62328644	T-47D	breast:	n/a	chr11:62328021-62328031
25	GATA3	chr11:62327940-62328732	MCF-7	breast:	n/a	chr11:62328021-62328031
26	POLR2A	chr11:62327811-62328621	HUVEC	blood vessel:	n/a	n/a
27	CHD2	chr11:62328015-62328556	Hela-S3	cervix:	n/a	n/a
28	SIN3AK20	chr11:62327943-62328670	SK-N-SH	brain:	n/a	n/a
29	TCF7L2	chr11:62328021-62328657	Hela-S3	cervix:	n/a	n/a
30	POLR2A	chr11:62328022-62328639	Hela-S3	cervix:	n/a	n/a
31	FOS	chr11:62327956-62328579	MCF10A-Er-Src	breast:	n/a	chr11:62328156-62328167 chr11:62328276-62328287 chr11:62328269-62328279 chr11:62328276-62328288 chr11:62328278-62328286 chr11:62328269-62328279
32	MAX	chr11:62327941-62328603	ECC-1	luminal epithelium:	n/a	n/a
33	RCOR1	chr11:62328011-62328716	Hela-S3	cervix:	n/a	n/a
34	RAD21	chr11:62327962-62328569	MCF-7	breast:	n/a	chr11:62328188-62328207 chr11:62328192-62328202 chr11:62328191-62328204 chr11:62328194-62328203
35	MAFK	chr11:62328090-62328563	K562	blood:	n/a	n/a
36	POLR2A	chr11:62327998-62328674	GM12892	blood:	n/a	n/a
37	CEBPB	chr11:62327974-62328690	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr11:62328025-62329123	HepG2	liver:	n/a	n/a
39	NR3C1	chr11:62327981-62328627	A549	lung:	n/a	chr11:62328278-62328287
40	SP1	chr11:62327838-62328759	HCT-116	colon:	n/a	n/a
41	TEAD4	chr11:62327868-62328562	HepG2	liver:	n/a	n/a
42	FOXA1	chr11:62328012-62328625	T-47D	breast:	n/a	n/a
43	CTCF	chr11:62327850-62328593	HCT-116	colon:	n/a	chr11:62328190-62328208 chr11:62328192-62328205 chr11:62328196-62328205
44	FOS	chr11:62328024-62328574	MCF10A-Er-Src	breast:	n/a	chr11:62328156-62328167 chr11:62328276-62328287 chr11:62328269-62328279 chr11:62328276-62328288 chr11:62328278-62328286 chr11:62328269-62328279
45	MAZ	chr11:62327836-62328665	IMR90	lung:	n/a	n/a
46	FOXA2	chr11:62328019-62328609	A549	lung:	n/a	n/a
47	GATA3	chr11:62327898-62328781	SK-N-SH	brain:	n/a	chr11:62328021-62328031
48	JUN	chr11:62327967-62328640	K562	blood:	n/a	chr11:62328156-62328167 chr11:62328269-62328279 chr11:62328276-62328288 chr11:62328278-62328286 chr11:62328269-62328279
49	USF2	chr11:62328003-62328588	Hela-S3	cervix:	n/a	n/a
50	POLR2A	chr11:62327895-62328579	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:62328062..62329768-chr11:62438392..62441181,2	K562	blood:
2	chr11:62312620..62313831-chr11:62327711..62328644,5	MCF-7	breast:
3	chr11:62320231..62322469-chr11:62326560..62328980,3	MCF-7	breast:
4	chr11:62326694..62329016-chr11:62431691..62434096,3	K562	blood:
5	chr11:62191885..62193096-chr11:62327580..62328641,7	K562	blood:
6	chr11:62326831..62332617-chr11:62337718..62342722,6	MCF-7	breast:
7	chr11:62264317..62265342-chr11:62327741..62328654,8	MCF-7	breast:
8	chr11:62326922..62329969-chr11:62332380..62335184,3	MCF-7	breast:
9	chr11:62309955..62311757-chr11:62327769..62328678,8	MCF-7	breast:
10	chr11:62162213..62162907-chr11:62327773..62328564,5	MCF-7	breast:
11	chr11:62328251..62329774-chr11:62605498..62607870,2	MCF-7	breast:
12	chr11:62319256..62325692-chr11:62326835..62334390,9	K562	blood:
13	chr11:62326979..62329934-chr11:62331462..62336636,5	K562	blood:
14	chr11:62328044..62331009-chr11:62411420..62414056,2	MCF-7	breast:
15	chr11:62275811..62278092-chr11:62326912..62329535,2	MCF-7	breast:
16	chr11:62275619..62276391-chr11:62327954..62328806,2	MCF-7	breast:
17	chr11:62328251..62330018-chr11:62332722..62335121,2	MCF-7	breast:
18	chr11:62191881..62192461-chr11:62327872..62328955,3	MCF-7	breast:
19	chr11:62326681..62329872-chr11:62430433..62433667,3	MCF-7	breast:
20	chr11:62328388..62330000-chr11:62343095..62344668,2	K562	blood:
21	chr11:62328250..62330762-chr11:62331688..62334513,2	K562	blood:

Variant related genes	Relation type
AHNAK	TF binding region
ENSG00000254772	Chromatin interaction
ENSG00000206597	Chromatin interaction
ENSG00000214756	Chromatin interaction
ENSG00000255432	Chromatin interaction
ENSG00000257058	Chromatin interaction
ENSG00000124942	Chromatin interaction
ENSG00000204922	Chromatin interaction
ENSG00000255508	Chromatin interaction
ENSG00000133316	Chromatin interaction
ENSG00000162194	Chromatin interaction

Extended variants
information (count: 62 )
Associated
traits (count: 12 )

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs1061093	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11231137	0.97[ASN][1000 genomes]
rs11231138	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11231141	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11231144	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11231145	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11231150	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11231151	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11231152	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11231154	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11231155	0.90[ASW][hapmap];0.96[CEU][hapmap];0.88[CHB][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11231156	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11231161	0.96[CEU][hapmap];0.84[GIH][hapmap];0.92[MEX][hapmap];0.88[TSI][hapmap];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11231176	1.00[JPT][hapmap]
rs11553576	0.96[CEU][hapmap];0.81[GIH][hapmap];0.92[MEX][hapmap];0.83[TSI][hapmap];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12049914	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12223627	0.83[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs12225213	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12226821	0.81[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs12808829	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17773169	0.92[CEU][hapmap];1.00[CHB][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.98[TSI][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1801144	0.92[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2428548	0.87[CEU][hapmap];1.00[CHB][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2428549	0.87[CEU][hapmap];1.00[CHB][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2428551	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2509961	0.87[CEU][hapmap];1.00[CHB][hapmap];0.92[MEX][hapmap];0.86[TSI][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2509967	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2509982	0.87[CEU][hapmap];1.00[CHB][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2512562	0.87[CEU][hapmap];1.00[CHB][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2512563	0.91[CEU][hapmap];1.00[CHB][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2516633	0.88[CHB][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.84[TSI][hapmap]
rs2516634	0.89[EUR][1000 genomes]
rs2849030	0.96[CEU][hapmap];0.88[CHB][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.90[TSI][hapmap];0.87[EUR][1000 genomes]
rs2849031	0.96[CEU][hapmap];0.88[CHB][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.93[TSI][hapmap];0.88[EUR][1000 genomes]
rs34065644	0.80[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs34894392	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35156678	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.81[MKK][hapmap];0.93[TSI][hapmap]
rs35587183	1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.88[TSI][hapmap];0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs35880596	0.96[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs58720921	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs60098285	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61296092	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7124057	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71490390	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71490392	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs71490394	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs72927213	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7928833	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7930896	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7937146	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7942154	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7942991	0.89[ASW][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.91[TSI][hapmap];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv915636	chr11:62016992-62713565	Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1441 gene(s)	inside rSNPs	diseases
2	nsv532283	chr11:62201358-62863475	Enhancers Flanking Active TSS Genic enhancers Strong transcription Weak transcription Active TSS Bivalent/Poised 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 miRNA target site	1433 gene(s)	inside rSNPs	diseases
3	nsv832180	chr11:62201605-62364828	Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Weak 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 miRNA miRNA target site	138 gene(s)	inside rSNPs	diseases
4	nsv532284	chr11:62220043-62630253	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers Active TSS Strong transcription 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	1401 gene(s)	inside rSNPs	diseases
5	esv3584599	chr11:62262742-62398050	Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
6	esv1801128	chr11:62276347-62329897	Flanking Active TSS Strong transcription Active TSS Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	62 gene(s)	inside rSNPs	diseases
7	esv1831183	chr11:62276347-62329897	Transcr. at gene 5' and 3' Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	62 gene(s)	inside rSNPs	diseases
8	nsv832182	chr11:62295575-62462848	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	245 gene(s)	inside rSNPs	diseases
9	nsv347	chr11:62297068-62338927	Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Genic 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	65 gene(s)	inside rSNPs	diseases
10	nsv825939	chr11:62326083-62410577	Flanking Active TSS Genic enhancers Strong transcription Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	122 gene(s)	inside rSNPs	diseases

mRNA abundance (count:12)

SNP	Gene	Cis/trans	Tissue	Source
rs7943191	EEF1G///LOC729998	N/A	lymphoblastoid	RTeQTL
rs7943191	MTA2	cis	Esophagus Mucosa	GTEx
rs7943191	EML3	cis	Whole Blood	GTEx
rs7943191	C11orf48	cis	cerebellum	SCAN
rs7943191	SCYL1	cis	parietal	SCAN
rs7943191	EEF1G	cis	multi-tissue	Pritchard
rs7943191	ROM1	cis	Thyroid	GTEx
rs7943191	CFL1	cis	parietal	SCAN
rs7943191	SLC22A25	cis	parietal	SCAN
rs7943191	TUT1	cis	parietal	SCAN
rs7943191	EML3	cis	cerebellum	SCAN
rs7943191	EML3	cis	Esophagus Mucosa	GTEx

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:62322400-62340000	Strong transcription	Fetal Brain Female	brain
2	chr11:62322600-62331200	Weak transcription	Ovary	ovary
3	chr11:62324200-62329000	Genic enhancers	Fetal Muscle Leg	muscle
4	chr11:62324400-62328600	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr11:62324400-62328800	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr11:62324600-62331600	Genic enhancers	Placenta	Placenta
7	chr11:62324800-62329000	Strong transcription	Cortex derived primary cultured neurospheres	brain
8	chr11:62324800-62329600	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr11:62324800-62330000	Genic enhancers	HMEC	breast
10	chr11:62324800-62333600	Weak transcription	Small Intestine	intestine
11	chr11:62324800-62338800	Strong transcription	Brain Germinal Matrix	brain
12	chr11:62324800-62339600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr11:62325000-62329000	Strong transcription	Fetal Stomach	stomach
14	chr11:62325000-62331200	Weak transcription	Psoas Muscle	Psoas
15	chr11:62325000-62331800	Genic enhancers	A549	lung
16	chr11:62325000-62338600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr11:62325000-62338800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr11:62325200-62329800	Strong transcription	Thymus	Thymus
19	chr11:62325200-62339600	Strong transcription	Primary neutrophils fromperipheralblood	blood
20	chr11:62325400-62328800	Strong transcription	Spleen	Spleen
21	chr11:62325600-62328600	Strong transcription	Brain Inferior Temporal Lobe	brain
22	chr11:62325600-62328600	Genic enhancers	Dnd41	blood
23	chr11:62325600-62329400	Strong transcription	Brain Cingulate Gyrus	brain
24	chr11:62325800-62329200	Genic enhancers	Rectal Mucosa Donor 29	rectum
25	chr11:62326000-62328600	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
26	chr11:62326000-62328600	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
27	chr11:62326000-62328600	Genic enhancers	NHDF-Ad	bronchial
28	chr11:62326000-62329800	Genic enhancers	HUVEC	blood vessel
29	chr11:62326000-62330000	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr11:62326200-62328600	Genic enhancers	Primary T cells fromperipheralblood	blood
31	chr11:62326200-62328600	Genic enhancers	Primary hematopoietic stem cells	blood
32	chr11:62326200-62328600	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
33	chr11:62326200-62328600	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
34	chr11:62326200-62328600	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
35	chr11:62326200-62328600	Genic enhancers	Primary T killer naive cells fromperipheralblood	blood
36	chr11:62326200-62328600	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr11:62326200-62328600	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr11:62326200-62328800	Genic enhancers	H1 Cell Line	embryonic stem cell
39	chr11:62326200-62328800	Genic enhancers	Primary T helper cells PMA-I stimulated	--
40	chr11:62326200-62328800	Genic enhancers	Duodenum Mucosa	Duodenum
41	chr11:62326200-62329400	Genic enhancers	K562	blood
42	chr11:62326200-62329400	Genic enhancers	NH-A	brain
43	chr11:62326200-62330400	Strong transcription	Fetal Kidney	kidney
44	chr11:62326400-62328600	Genic enhancers	Primary T helper cells fromperipheralblood	blood
45	chr11:62326400-62328600	Genic enhancers	Primary T killer memory cells from peripheral blood	blood
46	chr11:62326400-62330200	Strong transcription	Primary T cells from cord blood	blood
47	chr11:62326400-62339200	Strong transcription	Fetal Thymus	thymus
48	chr11:62326600-62328800	Genic enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr11:62326800-62328800	Genic enhancers	HSMMtube	muscle
50	chr11:62326800-62329000	Genic enhancers	HUES64 Cell Line	embryonic stem cell

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