Variant report

Variant	rs7641224
Chromosome Location	chr3:50307111-50307112
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:22)
CpG islands
(count:0)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:22 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MXI1	chr3:50306280-50307826	HepG2	liver:	n/a	chr3:50307004-50307019
2	POLR2A	chr3:50306407-50307549	HepG2	liver:	n/a	n/a
3	ZBTB7A	chr3:50305971-50307182	ECC-1	luminal epithelium:	n/a	n/a
4	SMARCB1	chr3:50305961-50309446	Hela-S3	cervix:	n/a	n/a
5	MAZ	chr3:50304153-50308532	IMR90	lung:	n/a	chr3:50306954-50306964
6	POLR2A	chr3:50305179-50309393	HepG2	liver:	n/a	n/a
7	POLR2A	chr3:50305651-50309364	Hela-S3	cervix:	n/a	n/a
8	GTF2F1	chr3:50306961-50307347	Hela-S3	cervix:	n/a	n/a
9	MAX	chr3:50305764-50309483	HepG2	liver:	n/a	chr3:50307440-50307450 chr3:50306954-50306964
10	HCFC1	chr3:50305717-50309480	Hela-S3	cervix:	n/a	n/a
11	POLR2A	chr3:50306412-50307180	HepG2	liver:	n/a	n/a
12	ZBTB7A	chr3:50306125-50307257	ECC-1	luminal epithelium:	n/a	n/a
13	MAX	chr3:50306070-50307954	Hela-S3	cervix:	n/a	chr3:50307440-50307450 chr3:50306954-50306964
14	POLR2A	chr3:50305532-50313853	HepG2	liver:	n/a	n/a
15	POLR2A	chr3:50305989-50309086	MCF-7	breast:	n/a	n/a
16	TFAP2C	chr3:50305566-50307587	Hela-S3	cervix:	n/a	n/a
17	RFX5	chr3:50307102-50307176	HepG2	liver:	n/a	chr3:50307139-50307154
18	POLR2A	chr3:50305961-50307411	Hela-S3	cervix:	n/a	n/a
19	MAX	chr3:50305555-50307825	Hela-S3	cervix:	n/a	chr3:50307440-50307450 chr3:50306954-50306964
20	POLR2A	chr3:50305828-50309562	Hela-S3	cervix:	n/a	n/a
21	POLR2A	chr3:50301468-50308558	ECC-1	luminal epithelium:	n/a	n/a
22	CHD2	chr3:50307105-50307190	HepG2	liver:	n/a	n/a

No data

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:50281584..50285263-chr3:50304924..50308731,5	MCF-7	breast:
2	chr3:50305661..50309418-chr3:50646590..50649218,4	MCF-7	breast:
3	chr3:50303839..50307896-chr3:50307992..50312285,6	K562	blood:
4	chr3:50229772..50232477-chr3:50306774..50308819,2	K562	blood:
5	chr3:50288326..50289923-chr3:50306596..50308969,2	MCF-7	breast:
6	chr3:50305641..50310504-chr3:50314554..50317584,4	K562	blood:
7	chr3:50263554..50267133-chr3:50306867..50310561,4	K562	blood:
8	chr3:50305234..50312110-chr3:50326257..50332221,8	MCF-7	breast:
9	chr3:50296030..50318456-chr3:50318822..50339499,66	MCF-7	breast:
10	chr3:50230717..50232832-chr3:50306481..50309139,3	MCF-7	breast:
11	chr3:50220929..50223103-chr3:50305394..50307626,2	K562	blood:
12	chr3:50300460..50314689-chr3:50349154..50363682,34	MCF-7	breast:
13	chr3:50263019..50266611-chr3:50304390..50308892,11	MCF-7	breast:
14	chr3:50266814..50271565-chr3:50304984..50308896,4	MCF-7	breast:
15	chr3:50271706..50275857-chr3:50303511..50313889,17	MCF-7	breast:

No data

Variant related genes	Relation type
SEMA3B-AS1	TF binding region
SEMA3B	TF binding region
ENSG00000214706	Chromatin interaction
ENSG00000114378	Chromatin interaction
ENSG00000186792	Chromatin interaction
ENSG00000114353	Chromatin interaction
ENSG00000114737	Chromatin interaction
ENSG00000179564	Chromatin interaction
ENSG00000114738	Chromatin interaction
ENSG00000012171	Chromatin interaction
ENSG00000114349	Chromatin interaction
ENSG00000243477	Chromatin interaction
ENSG00000068001	Chromatin interaction
ENSG00000001617	Chromatin interaction

Extended variants
information (count: 85 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs1034408	1.00[CEU][hapmap]
rs1034409	1.00[CEU][hapmap]
rs11914549	0.82[EUR][1000 genomes]
rs11916258	1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.85[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11928538	1.00[GIH][hapmap]
rs1894324	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.95[EUR][1000 genomes]
rs2157328	1.00[CEU][hapmap]
rs2187815	1.00[CEU][hapmap]
rs2236944	1.00[CEU][hapmap];0.85[GIH][hapmap];1.00[TSI][hapmap]
rs2236969	1.00[CEU][hapmap]
rs2236972	1.00[CEU][hapmap]
rs2236977	1.00[CEU][hapmap]
rs2236978	1.00[CEU][hapmap]
rs2236982	1.00[CEU][hapmap]
rs2282754	0.82[YRI][hapmap]
rs2282757	1.00[CEU][hapmap]
rs2298953	1.00[CEU][hapmap];0.85[GIH][hapmap];1.00[TSI][hapmap]
rs2298954	1.00[CEU][hapmap];0.85[GIH][hapmap];1.00[TSI][hapmap]
rs35742391	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3774753	1.00[CEU][hapmap];0.85[GIH][hapmap]
rs56287038	0.82[EUR][1000 genomes]
rs57453427	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58415636	0.82[EUR][1000 genomes]
rs61382127	0.82[EUR][1000 genomes]
rs6446203	1.00[CEU][hapmap];1.00[GIH][hapmap];0.82[EUR][1000 genomes]
rs6767505	1.00[CEU][hapmap]
rs6768830	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6770258	1.00[CEU][hapmap]
rs6770669	1.00[CEU][hapmap]
rs743754	1.00[CEU][hapmap]
rs743755	1.00[CEU][hapmap]
rs743859	1.00[CEU][hapmap]
rs7626470	1.00[CEU][hapmap]
rs7629917	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7634307	1.00[CEU][hapmap]
rs7636862	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.95[EUR][1000 genomes]
rs7647409	1.00[CEU][hapmap]
rs7649603	1.00[CEU][hapmap]
rs886075	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9817768	1.00[CEU][hapmap]
rs9828829	1.00[CEU][hapmap]
rs9830408	1.00[CEU][hapmap]
rs9836046	0.95[EUR][1000 genomes]
rs9837658	1.00[CEU][hapmap]
rs9851719	1.00[EUR][1000 genomes]
rs9854585	1.00[CEU][hapmap]
rs9863307	1.00[CEU][hapmap]
rs9875873	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][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];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9878345	1.00[EUR][1000 genomes]
rs9883222	1.00[CEU][hapmap];0.85[GIH][hapmap];1.00[TSI][hapmap]
rs9883635	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:34 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1001775	chr3:50129479-50311666	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv523662	chr3:50144951-50584999	Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
3	nsv1013949	chr3:50151712-50339163	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
4	nsv590250	chr3:50153356-50332697	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active 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 miRNA target site	43 gene(s)	inside rSNPs	diseases
5	nsv876769	chr3:50155468-50408398	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription 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	94 gene(s)	inside rSNPs	diseases
6	esv1821728	chr3:50156142-50657253	Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
7	esv1793751	chr3:50157364-50476363	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
8	esv1828162	chr3:50157364-50506151	Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription 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	98 gene(s)	inside rSNPs	diseases
9	nsv590251	chr3:50158774-50337422	Active TSS Strong transcription Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
10	nsv470561	chr3:50158774-50584999	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Bivalent Enhancer Strong transcription 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 miRNA target site	99 gene(s)	inside rSNPs	diseases
11	nsv876770	chr3:50158774-50609624	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
12	nsv523560	chr3:50172397-50339163	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
13	nsv460529	chr3:50178011-50324672	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
14	nsv460530	chr3:50178011-50324672	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
15	nsv590252	chr3:50178011-50324672	Enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
16	nsv1002916	chr3:50187646-50311666	Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
17	nsv536564	chr3:50187646-50311666	Flanking Active TSS Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
18	nsv1014256	chr3:50187646-50339163	Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Bivalent/Poised TSS Flanking 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 miRNA target site	53 gene(s)	inside rSNPs	diseases
19	nsv536565	chr3:50187646-50339163	Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Enhancers Weak transcription Genic enhancers 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 miRNA target site	53 gene(s)	inside rSNPs	diseases
20	nsv1001993	chr3:50187646-50640808	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
21	nsv590253	chr3:50196418-50337422	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
22	esv2757870	chr3:50198478-50371377	Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
23	esv2759148	chr3:50198478-50371377	Enhancers Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
24	nsv834692	chr3:50198485-50393464	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
25	nsv590254	chr3:50243510-50388607	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
26	nsv460531	chr3:50247824-50436827	Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
27	nsv590255	chr3:50247824-50436827	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
28	nsv876772	chr3:50255305-50436827	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
29	nsv590257	chr3:50302830-50393640	Genic enhancers Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
30	nsv590256	chr3:50302830-50420554	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS 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	83 gene(s)	inside rSNPs	diseases
31	nsv876774	chr3:50302830-50436827	Enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak 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	83 gene(s)	inside rSNPs	diseases
32	nsv876773	chr3:50302830-50480131	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
33	nsv834693	chr3:50302830-50507964	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
34	esv3404854	chr3:50305373-50307921	Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:50300600-50307800	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr3:50300800-50307400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr3:50300800-50307600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr3:50301000-50307200	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr3:50301000-50307600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr3:50301000-50308200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr3:50301200-50307600	Enhancers	H1 Cell Line	embryonic stem cell
8	chr3:50301600-50307600	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr3:50302400-50307800	Flanking Active TSS	Stomach Smooth Muscle	stomach
10	chr3:50302600-50309600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr3:50303600-50307800	Enhancers	Sigmoid Colon	Sigmoid Colon
12	chr3:50303600-50307800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
13	chr3:50304000-50308000	Flanking Active TSS	Colonic Mucosa	Colon
14	chr3:50304000-50308000	Flanking Active TSS	NHLF	lung
15	chr3:50304000-50308600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr3:50304200-50307800	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr3:50304400-50307600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr3:50304400-50307600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
19	chr3:50304600-50307600	Enhancers	Spleen	Spleen
20	chr3:50304800-50307600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr3:50304800-50309000	Weak transcription	K562	blood
22	chr3:50305000-50307600	Enhancers	Brain Germinal Matrix	brain
23	chr3:50305000-50307800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr3:50305200-50307400	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
25	chr3:50305200-50309000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr3:50305400-50307200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
27	chr3:50305400-50308000	Flanking Active TSS	Brain Hippocampus Middle	brain
28	chr3:50305400-50308600	Enhancers	Esophagus	oesophagus
29	chr3:50305600-50307200	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr3:50305600-50307800	Flanking Active TSS	Brain Anterior Caudate	brain
31	chr3:50305600-50308400	Enhancers	NH-A	brain
32	chr3:50305600-50308600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr3:50305600-50310600	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr3:50305800-50307200	Flanking Active TSS	Rectal Smooth Muscle	rectum
35	chr3:50305800-50308000	Enhancers	Fetal Heart	heart
36	chr3:50305800-50308400	Enhancers	NHEK	skin
37	chr3:50305800-50308600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr3:50305800-50309800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr3:50306000-50307800	Flanking Active TSS	Duodenum Mucosa	Duodenum
40	chr3:50306000-50307800	Flanking Active TSS	Fetal Muscle Trunk	muscle
41	chr3:50306000-50307800	Flanking Active TSS	Osteobl	bone
42	chr3:50306000-50308200	Flanking Active TSS	Pancreas	Pancrea
43	chr3:50306000-50309000	Weak transcription	Liver	Liver
44	chr3:50306000-50309200	Enhancers	Fetal Lung	lung
45	chr3:50306000-50309400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr3:50306200-50307800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr3:50306200-50308000	Enhancers	Fetal Brain Male	brain
48	chr3:50306200-50308200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
49	chr3:50306200-50308200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr3:50306200-50308400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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