Variant report

Variant	rs6591825
Chromosome Location	chr11:63655122-63655123
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:9)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:9 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	E2F6	chr11:63654935-63655603	H1-hESC	embryonic stem cell:	n/a	n/a
2	E2F6	chr11:63655037-63655419	H1-hESC	embryonic stem cell:	n/a	n/a
3	MAX	chr11:63655015-63655479	H1-hESC	embryonic stem cell:	n/a	n/a
4	MAX	chr11:63654891-63655536	H1-hESC	embryonic stem cell:	n/a	n/a
5	POLR2A	chr11:63655032-63656617	HepG2	liver:	n/a	n/a
6	MAX	chr11:63654901-63656419	NB4	blood:	n/a	n/a
7	TEAD4	chr11:63655009-63656251	K562	blood:	n/a	chr11:63655606-63655615
8	MAX	chr11:63655070-63655453	H1-hESC	embryonic stem cell:	n/a	n/a
9	MAX	chr11:63655047-63655466	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:63655087-63655137	SKMC	muscle:	n/a
2	chr11:63655087-63655137	SK-N-MC	brain:	n/a
3	chr11:63655087-63655137	AG04450	lung:	fetal
4	chr11:63655087-63655137	GM12891	blood:	n/a
5	chr11:63655087-63655137	H1-hESC	embryonic stem cell:	embryo
6	chr11:63655087-63655137	LNCaP	prostate:	n/a
7	chr11:63655087-63655137	NB4	blood:	n/a
8	chr11:63655087-63655137	Caco-2	colon:	n/a
9	chr11:63655087-63655137	IMR90	lung:	fetal
10	chr11:63655087-63655137	RPTEC	kidney:	n/a
11	chr11:63655087-63655137	AG04449	skin:	fetal
12	chr11:63655087-63655137	ECC-1	luminal epithelium:	n/a
13	chr11:63655087-63655137	GM06990	blood:	n/a
14	chr11:63655087-63655137	AG10803	skin:	n/a
15	chr11:63655087-63655137	SK-N-SH	brain:	n/a
16	chr11:63655087-63655137	HEK293	kidney:	embryo
17	chr11:63655087-63655137	CMK	blood:	n/a
18	chr11:63655087-63655137	HAEpiC	amniotic membrane:	n/a
19	chr11:63655087-63655137	NT2-D1	testis:	n/a
20	chr11:63655087-63655137	MCF10A-Er-Src	breast:	n/a
21	chr11:63655087-63655137	NHBE	bronchial:	n/a
22	chr11:63655087-63655137	ProgFib	skin:	n/a
23	chr11:63655087-63655137	HCT-116	colon:	n/a
24	chr11:63655087-63655137	PANC-1	pancreas:	n/a
25	chr11:63655087-63655137	GM19239	blood:	n/a
26	chr11:63655087-63655137	BE2_C	brain:	n/a
27	chr11:63655087-63655137	BJ	skin:	n/a
28	chr11:63655087-63655137	HUVEC	blood vessel:	n/a
29	chr11:63655087-63655137	HRCEpiC	kidney:	n/a
30	chr11:63655087-63655137	AG09319	gingival:	n/a
31	chr11:63655087-63655137	Jurkat	blood:	n/a
32	chr11:63655087-63655137	U87	brain:	n/a
33	chr11:63655087-63655137	AG09309	skin:	n/a
34	chr11:63655087-63655137	SK-N-SH_RA	brain:	n/a
35	chr11:63655087-63655137	Hela-S3	cervix:	n/a
36	chr11:63655087-63655137	HPAEpiC	pulmonary alveolar:	n/a
37	chr11:63655087-63655137	HL-60	blood:	n/a
38	chr11:63655087-63655137	SAEC	small airway:	n/a
39	chr11:63655087-63655137	NHDF-neo	bronchial:	n/a
40	chr11:63655087-63655137	ovcar-3	ovarian:	n/a
41	chr11:63655087-63655137	HCF	heart:	n/a
42	chr11:63655087-63655137	AoSMC	blood vessel:	n/a
43	chr11:63655087-63655137	K562	blood:	n/a
44	chr11:63655087-63655137	T-47D	breast:	n/a
45	chr11:63655087-63655137	Hepatocyte	liver:	n/a
46	chr11:63655087-63655137	A549	lung:	n/a
47	chr11:63655087-63655137	HMEC	breast:	n/a
48	chr11:63655087-63655137	PrEC	prostate:	n/a
49	chr11:63655087-63655137	HNPCEpiC	eye:	n/a
50	chr11:63655087-63655137	HIPEpiC	eye:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:63639315..63642041-chr11:63653506..63655587,2	K562	blood:
2	chr11:63654599..63657425-chr11:63952225..63954812,2	K562	blood:
3	chr11:63653210..63656003-chr11:63665435..63667701,2	MCF-7	breast:
4	chr11:63581060..63583015-chr11:63654229..63655873,2	MCF-7	breast:

No data

Variant related genes	Relation type
RNU6-1306P	TF binding region
MARK2	TF binding region
MARK2	CpG island
RNU6-1306P	CpG island
ENSG00000168439	Chromatin interaction

Extended variants
information (count: 54 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10736731	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10751001	0.83[ASN][1000 genomes]
rs10792421	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.92[LWK][hapmap];0.94[MEX][hapmap];0.81[MKK][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10792422	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10792423	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10897452	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10897453	0.87[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];0.82[GIH][hapmap];0.90[JPT][hapmap];0.92[LWK][hapmap];0.98[MKK][hapmap];0.95[TSI][hapmap];0.86[YRI][hapmap];0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10897454	0.87[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.80[GIH][hapmap];1.00[JPT][hapmap];0.92[LWK][hapmap];0.83[MEX][hapmap];0.98[MKK][hapmap];0.98[TSI][hapmap];0.88[YRI][hapmap];0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11231600	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11231606	0.84[EUR][1000 genomes]
rs11231624	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11231628	0.86[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs11231637	1.00[CEU][hapmap];0.98[GIH][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11231640	0.80[ASW][hapmap];0.89[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.84[LWK][hapmap];0.94[MEX][hapmap];0.95[TSI][hapmap];0.81[YRI][hapmap];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11231646	0.86[CHB][hapmap]
rs11605500	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12277481	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12576275	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1486936	1.00[CEU][hapmap];0.98[GIH][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1872772	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];0.98[TSI][hapmap];0.89[YRI][hapmap];0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2840079	0.89[CEU][hapmap];0.87[CHB][hapmap];0.80[CHD][hapmap];0.88[GIH][hapmap];0.90[JPT][hapmap];0.81[LWK][hapmap];0.94[MEX][hapmap];0.95[TSI][hapmap];0.81[YRI][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs320109	1.00[CEU][hapmap];0.98[GIH][hapmap];0.94[MEX][hapmap];0.93[TSI][hapmap];0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3802941	1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];0.93[GIH][hapmap];0.81[JPT][hapmap];0.96[LWK][hapmap];0.94[MEX][hapmap];0.89[MKK][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3850943	0.83[ASN][1000 genomes]
rs4143327	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4963433	0.83[ASN][1000 genomes]
rs4980503	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4980505	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4980507	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4980528	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4980529	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.94[YRI][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4980532	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4980533	0.94[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61604723	0.81[EUR][1000 genomes]
rs6421686	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7102006	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7105288	1.00[CEU][hapmap];0.98[GIH][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7108375	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7110843	0.94[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7118913	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7121067	0.90[EUR][1000 genomes]
rs7937314	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7939351	0.82[EUR][1000 genomes]
rs7944519	0.87[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.80[GIH][hapmap];1.00[JPT][hapmap];0.92[LWK][hapmap];0.94[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];0.88[YRI][hapmap];0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7946503	0.81[EUR][1000 genomes]
rs7948656	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs923247	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs928948	0.86[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051171	chr11:62987064-63835715	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	100 gene(s)	inside rSNPs	diseases
2	nsv468589	chr11:63515752-63713239	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv555180	chr11:63515752-63713239	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	esv1839119	chr11:63615554-63680052	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	8 gene(s)	inside rSNPs	diseases
5	nsv468590	chr11:63639881-63783352	Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
6	nsv555181	chr11:63639881-63783352	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs6591825	ZBTB3	cis	parietal	SCAN
rs6591825	NAALADL1	cis	cerebellum	SCAN
rs6591825	DPF2	cis	parietal	SCAN
rs6591825	SLC22A11	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:63643600-63655800	Weak transcription	Aorta	Aorta
2	chr11:63644600-63655200	Enhancers	Primary T helper cells fromperipheralblood	blood
3	chr11:63648400-63655200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr11:63650600-63655600	Weak transcription	Fetal Muscle Trunk	muscle
5	chr11:63650800-63656000	Weak transcription	Brain Germinal Matrix	brain
6	chr11:63650800-63657600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr11:63651200-63655600	Genic enhancers	Fetal Intestine Small	intestine
8	chr11:63652000-63659600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr11:63652200-63659400	Weak transcription	Fetal Brain Female	brain
10	chr11:63652600-63655200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr11:63653600-63655200	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr11:63653600-63655200	Enhancers	Dnd41	blood
13	chr11:63653600-63655400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
14	chr11:63653600-63655600	Enhancers	Primary T cells fromperipheralblood	blood
15	chr11:63653600-63655800	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr11:63653800-63655200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
17	chr11:63653800-63655200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
18	chr11:63653800-63655200	Enhancers	K562	blood
19	chr11:63653800-63655600	Enhancers	Primary B cells from peripheral blood	blood
20	chr11:63653800-63655600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
21	chr11:63653800-63655600	Enhancers	Left Ventricle	heart
22	chr11:63653800-63656000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr11:63653800-63656000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr11:63654200-63655200	Enhancers	Primary T helper naive cells from peripheral blood	blood
25	chr11:63654200-63655200	Enhancers	Thymus	Thymus
26	chr11:63654200-63655600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr11:63654200-63655600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
28	chr11:63654200-63656000	Enhancers	Brain Hippocampus Middle	brain
29	chr11:63654200-63656000	Enhancers	Sigmoid Colon	Sigmoid Colon
30	chr11:63654200-63656400	Enhancers	A549	lung
31	chr11:63654200-63658000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr11:63654200-63658400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
33	chr11:63654400-63655200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
34	chr11:63654400-63655200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr11:63654400-63655200	Enhancers	Muscle Satellite Cultured Cells	--
36	chr11:63654400-63655400	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr11:63654400-63655400	Enhancers	Small Intestine	intestine
38	chr11:63654400-63655600	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr11:63654400-63655600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
40	chr11:63654400-63655600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr11:63654400-63655600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr11:63654400-63655600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
43	chr11:63654400-63655600	Enhancers	Adipose Nuclei	Adipose
44	chr11:63654400-63655600	Enhancers	Liver	Liver
45	chr11:63654400-63655600	Enhancers	Duodenum Smooth Muscle	Duodenum
46	chr11:63654400-63655600	Enhancers	Fetal Intestine Large	intestine
47	chr11:63654400-63655600	Enhancers	Pancreas	Pancrea
48	chr11:63654400-63655600	Enhancers	Skeletal Muscle Female	skeletal muscle
49	chr11:63654400-63655600	Enhancers	Stomach Mucosa	stomach
50	chr11:63654400-63655600	Enhancers	Stomach Smooth Muscle	stomach

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