Variant report

Variant	rs11231144
Chromosome Location	chr11:62328038-62328039
allele	C/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	SIN3AK20	chr11:62327934-62328464	A549	lung:	n/a	n/a
2	HNF4A	chr11:62328019-62328288	HepG2	liver:	n/a	n/a
3	RAD21	chr11:62327890-62328598	MCF-7	breast:	n/a	chr11:62328188-62328207 chr11:62328192-62328202 chr11:62328191-62328204 chr11:62328194-62328203
4	CTCF	chr11:62327984-62328419	H1-hESC	embryonic stem cell:	n/a	chr11:62328190-62328208 chr11:62328192-62328205 chr11:62328196-62328205
5	POLR2A	chr11:62327831-62328765	PANC-1	pancreas:	n/a	n/a
6	FOXM1	chr11:62327817-62328457	GM12878	blood:	n/a	chr11:62328404-62328412
7	NR2F2	chr11:62327727-62328650	K562	blood:	n/a	n/a
8	FOXA2	chr11:62328014-62328439	HepG2	liver:	n/a	n/a
9	POLR2A	chr11:62327962-62328579	HCT-116	colon:	n/a	n/a
10	BRCA1	chr11:62327977-62328618	Hela-S3	cervix:	n/a	n/a
11	POLR2A	chr11:62327469-62328801	PFSK-1	brain:	n/a	n/a
12	MYBL2	chr11:62327917-62328571	HepG2	liver:	n/a	n/a
13	SIN3AK20	chr11:62327917-62328679	PANC-1	pancreas:	n/a	n/a
14	RXRA	chr11:62327936-62328783	SK-N-SH	brain:	n/a	chr11:62328188-62328208
15	MAX	chr11:62327908-62328533	SK-N-SH	brain:	n/a	n/a
16	MAZ	chr11:62328019-62328590	Hela-S3	cervix:	n/a	n/a
17	POLR2A	chr11:62328011-62328326	A549	lung:	n/a	n/a
18	SMC3	chr11:62328013-62328447	K562	blood:	n/a	chr11:62328192-62328206
19	RAD21	chr11:62327845-62328791	SK-N-SH	brain:	n/a	chr11:62328188-62328207 chr11:62328192-62328202 chr11:62328191-62328204 chr11:62328194-62328203
20	MYC	chr11:62328001-62328519	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr11:62327917-62328490	U87	brain:	n/a	n/a
22	TCF12	chr11:62327885-62328896	SK-N-SH	brain:	n/a	n/a
23	MAX	chr11:62328030-62328373	K562	blood:	n/a	n/a
24	POLR2A	chr11:62327982-62328446	ECC-1	luminal epithelium:	n/a	n/a
25	MXI1	chr11:62327925-62328599	Hela-S3	cervix:	n/a	n/a
26	SP1	chr11:62327868-62328387	H1-hESC	embryonic stem cell:	n/a	n/a
27	RAD21	chr11:62327989-62328454	A549	lung:	n/a	chr11:62328188-62328207 chr11:62328192-62328202 chr11:62328191-62328204 chr11:62328194-62328203
28	NFIC	chr11:62328024-62328421	HepG2	liver:	n/a	n/a
29	TCF12	chr11:62327951-62328851	SK-N-SH	brain:	n/a	n/a
30	RAD21	chr11:62327989-62328400	GM12878	blood:	n/a	chr11:62328188-62328207 chr11:62328192-62328202 chr11:62328191-62328204 chr11:62328194-62328203
31	EP300	chr11:62328020-62328631	Hela-S3	cervix:	n/a	n/a
32	RAD21	chr11:62328020-62328414	K562	blood:	n/a	chr11:62328188-62328207 chr11:62328192-62328202 chr11:62328191-62328204 chr11:62328194-62328203
33	POLR2A	chr11:62326857-62328682	GM12892	blood:	n/a	n/a
34	MAX	chr11:62327841-62328642	A549	lung:	n/a	n/a
35	RAD21	chr11:62327989-62328379	H1-hESC	embryonic stem cell:	n/a	chr11:62328188-62328207 chr11:62328192-62328202 chr11:62328191-62328204 chr11:62328194-62328203
36	EP300	chr11:62327905-62328370	H1-hESC	embryonic stem cell:	n/a	n/a
37	TBP	chr11:62328017-62328567	Hela-S3	cervix:	n/a	n/a
38	JUN	chr11:62328022-62328463	H1-hESC	embryonic stem cell:	n/a	chr11:62328156-62328167 chr11:62328269-62328279 chr11:62328276-62328288 chr11:62328278-62328286 chr11:62328269-62328279
39	ZKSCAN1	chr11:62328009-62328557	Hela-S3	cervix:	n/a	n/a
40	MXI1	chr11:62328027-62328340	GM12878	blood:	n/a	n/a
41	FOSL2	chr11:62327856-62328568	A549	lung:	n/a	chr11:62328156-62328167 chr11:62328269-62328279 chr11:62328276-62328288 chr11:62328278-62328286 chr11:62328269-62328279
42	GATA3	chr11:62327989-62328644	T-47D	breast:	n/a	chr11:62328021-62328031
43	POU2F2	chr11:62328031-62328292	GM12878	blood:	n/a	n/a
44	SIN3A	chr11:62328026-62328445	H1-hESC	embryonic stem cell:	n/a	n/a
45	GATA3	chr11:62327940-62328732	MCF-7	breast:	n/a	chr11:62328021-62328031
46	MAX	chr11:62328038-62328383	K562	blood:	n/a	n/a
47	POLR2A	chr11:62327811-62328621	HUVEC	blood vessel:	n/a	n/a
48	POLR2A	chr11:62327796-62328475	HUVEC	blood vessel:	n/a	n/a
49	CHD2	chr11:62328015-62328556	Hela-S3	cervix:	n/a	n/a
50	RCOR1	chr11:62328020-62328472	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:62312620..62313831-chr11:62327711..62328644,5	MCF-7	breast:
2	chr11:62326694..62328330-chr11:62431691..62433227,2	K562	blood:
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	chr11:62191933..62192862-chr11:62327773..62328477,2	MCF-7	breast:
12	chr11:62319256..62325692-chr11:62326835..62334390,9	K562	blood:
13	chr11:62326979..62329934-chr11:62331462..62336636,5	K562	blood:
14	chr11:62326740..62328480-chr11:62359230..62362126,2	K562	blood:
15	chr11:62275811..62278092-chr11:62326912..62329535,2	MCF-7	breast:
16	chr11:62275619..62276391-chr11:62327954..62328806,2	MCF-7	breast:
17	chr11:62191881..62192461-chr11:62327872..62328955,3	MCF-7	breast:
18	chr11:62166890..62167441-chr11:62327708..62328242,2	K562	blood:
19	chr11:62309977..62310808-chr11:62327801..62328330,2	MCF-7	breast:
20	chr11:62326681..62329872-chr11:62430433..62433667,3	MCF-7	breast:
21	chr11:62162075..62162962-chr11:62327729..62328506,4	K562	blood:

Variant related genes	Relation type
AHNAK	TF binding region
ENSG00000206597	Chromatin interaction
ENSG00000214756	Chromatin interaction
ENSG00000254772	Chromatin interaction
ENSG00000257058	Chromatin interaction
ENSG00000149016	Chromatin interaction
ENSG00000255432	Chromatin interaction
ENSG00000124942	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];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11231137	0.80[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs11231138	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[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];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11231145	0.96[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];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11231151	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11231152	0.93[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];0.93[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];0.87[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];0.93[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];0.85[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[EUR][1000 genomes]
rs12049914	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12223627	0.80[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs12225213	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12226821	0.80[ASN][1000 genomes]
rs12808829	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];0.89[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];0.86[EUR][1000 genomes]
rs2428548	0.87[CEU][hapmap];1.00[CHB][hapmap];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2428549	0.87[CEU][hapmap];1.00[CHB][hapmap];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2428551	0.83[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];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2509967	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2509982	0.87[CEU][hapmap];1.00[CHB][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2512562	0.87[CEU][hapmap];1.00[CHB][hapmap];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2512563	0.91[CEU][hapmap];1.00[CHB][hapmap];0.84[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[ASN][1000 genomes]
rs34894392	0.83[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];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs35880596	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs58720921	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs60098285	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61296092	0.97[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];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71490390	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71490392	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs71490394	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs72927213	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7928833	0.94[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];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7937146	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7942154	0.80[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];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7943191	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]

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
rs11231144	TUT1	cis	parietal	SCAN
rs11231144	EML3	cis	multi-tissue	Pritchard
rs11231144	SLC22A25	cis	parietal	SCAN
rs11231144	ROM1	cis	Thyroid	GTEx
rs11231144	CFL1	cis	parietal	SCAN
rs11231144	C11orf48	cis	cerebellum	SCAN
rs11231144	MTA2	cis	Esophagus Mucosa	GTEx
rs11231144	EML3	cis	Esophagus Mucosa	GTEx
rs11231144	EML3	cis	cerebellum	SCAN
rs11231144	SCYL1	cis	parietal	SCAN
rs11231144	EML3	cis	Whole Blood	GTEx
rs11231144	EEF1G	cis	multi-tissue	Pritchard

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:62322400-62328200	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr11:62322400-62340000	Strong transcription	Fetal Brain Female	brain
3	chr11:62322600-62331200	Weak transcription	Ovary	ovary
4	chr11:62324200-62329000	Genic enhancers	Fetal Muscle Leg	muscle
5	chr11:62324400-62328200	Genic enhancers	HSMM	muscle
6	chr11:62324400-62328600	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr11:62324400-62328800	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr11:62324600-62331600	Genic enhancers	Placenta	Placenta
9	chr11:62324800-62328200	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr11:62324800-62329000	Strong transcription	Cortex derived primary cultured neurospheres	brain
11	chr11:62324800-62329600	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr11:62324800-62330000	Genic enhancers	HMEC	breast
13	chr11:62324800-62333600	Weak transcription	Small Intestine	intestine
14	chr11:62324800-62338800	Strong transcription	Brain Germinal Matrix	brain
15	chr11:62324800-62339600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr11:62325000-62328400	Genic enhancers	Hela-S3	cervix
17	chr11:62325000-62329000	Strong transcription	Fetal Stomach	stomach
18	chr11:62325000-62331200	Weak transcription	Psoas Muscle	Psoas
19	chr11:62325000-62331800	Genic enhancers	A549	lung
20	chr11:62325000-62338600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr11:62325000-62338800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr11:62325200-62329800	Strong transcription	Thymus	Thymus
23	chr11:62325200-62339600	Strong transcription	Primary neutrophils fromperipheralblood	blood
24	chr11:62325400-62328800	Strong transcription	Spleen	Spleen
25	chr11:62325600-62328600	Strong transcription	Brain Inferior Temporal Lobe	brain
26	chr11:62325600-62328600	Genic enhancers	Dnd41	blood
27	chr11:62325600-62329400	Strong transcription	Brain Cingulate Gyrus	brain
28	chr11:62325800-62329200	Genic enhancers	Rectal Mucosa Donor 29	rectum
29	chr11:62326000-62328600	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
30	chr11:62326000-62328600	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
31	chr11:62326000-62328600	Genic enhancers	NHDF-Ad	bronchial
32	chr11:62326000-62329800	Genic enhancers	HUVEC	blood vessel
33	chr11:62326000-62330000	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr11:62326200-62328200	Genic enhancers	H9 Cell Line	embryonic stem cell
35	chr11:62326200-62328200	Genic enhancers	NHLF	lung
36	chr11:62326200-62328400	Strong transcription	Brain Angular Gyrus	brain
37	chr11:62326200-62328400	Strong transcription	Gastric	stomach
38	chr11:62326200-62328600	Genic enhancers	Primary T cells fromperipheralblood	blood
39	chr11:62326200-62328600	Genic enhancers	Primary hematopoietic stem cells	blood
40	chr11:62326200-62328600	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
41	chr11:62326200-62328600	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chr11:62326200-62328600	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
43	chr11:62326200-62328600	Genic enhancers	Primary T killer naive cells fromperipheralblood	blood
44	chr11:62326200-62328600	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr11:62326200-62328600	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr11:62326200-62328800	Genic enhancers	H1 Cell Line	embryonic stem cell
47	chr11:62326200-62328800	Genic enhancers	Primary T helper cells PMA-I stimulated	--
48	chr11:62326200-62328800	Genic enhancers	Duodenum Mucosa	Duodenum
49	chr11:62326200-62329400	Genic enhancers	K562	blood
50	chr11:62326200-62329400	Genic enhancers	NH-A	brain

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