Variant report

Variant	rs3757423
Chromosome Location	chr7:150067714-150067715
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:43)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:43 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr7:150064930-150072034	GM12878	blood:	n/a	n/a
2	POLR2A	chr7:150067350-150067987	Hela-S3	cervix:	n/a	n/a
3	POLR2A	chr7:150065018-150068478	GM12878	blood:	n/a	n/a
4	POLR2A	chr7:150067686-150068008	H1-hESC	embryonic stem cell:	n/a	n/a
5	POLR2A	chr7:150065024-150068774	GM12892	blood:	n/a	n/a
6	POLR2A	chr7:150065045-150069575	GM18526	blood:	n/a	n/a
7	TBP	chr7:150067651-150068054	HepG2	liver:	n/a	n/a
8	POLR2A	chr7:150065010-150072093	GM12878	blood:	n/a	n/a
9	POLR2A	chr7:150064939-150068709	GM12878	blood:	n/a	n/a
10	CTCF	chr7:150067640-150067790	HRE	kidney:	n/a	n/a
11	TEAD4	chr7:150067697-150068174	HepG2	liver:	n/a	n/a
12	POLR2A	chr7:150065058-150068789	K562	blood:	n/a	n/a
13	POLR2A	chr7:150064808-150069359	K562	blood:	n/a	n/a
14	POLR2A	chr7:150065044-150070916	GM19193	blood:	n/a	n/a
15	POLR2A	chr7:150064841-150068822	HL-60	blood:	n/a	n/a
16	MXI1	chr7:150064165-150068175	SK-N-SH	brain:	n/a	chr7:150068088-150068103 chr7:150065688-150065703 chr7:150065860-150065869 chr7:150068090-150068105 chr7:150065686-150065701
17	HEY1	chr7:150065020-150068404	K562	blood:	n/a	chr7:150065245-150065260 chr7:150065724-150065739
18	CEBPB	chr7:150067666-150068010	HepG2	liver:	n/a	n/a
19	POLR2A	chr7:150064968-150071009	K562	blood:	n/a	n/a
20	POLR2A	chr7:150067692-150068378	HepG2	liver:	n/a	n/a
21	POLR2A	chr7:150065515-150069259	HepG2	liver:	n/a	n/a
22	POLR2A	chr7:150065009-150070940	GM18505	blood:	n/a	n/a
23	POLR2A	chr7:150064860-150068447	GM12891	blood:	n/a	n/a
24	POLR2A	chr7:150064952-150072087	GM12892	blood:	n/a	n/a
25	POLR2A	chr7:150064808-150068782	HepG2	liver:	n/a	n/a
26	RCOR1	chr7:150067625-150067839	GM12878	blood:	n/a	n/a
27	RCOR1	chr7:150064690-150068362	IMR90	lung:	n/a	n/a
28	POLR2A	chr7:150067172-150068109	GM12891	blood:	n/a	n/a
29	NR2F2	chr7:150066080-150067747	K562	blood:	n/a	n/a
30	POLR2A	chr7:150067653-150068108	MCF10A-Er-Src	breast:	n/a	n/a
31	POLR2A	chr7:150064843-150076606	K562	blood:	n/a	n/a
32	POLR2A	chr7:150067691-150068104	SK-N-SH	brain:	n/a	n/a
33	POLR2A	chr7:150067303-150068123	K562	blood:	n/a	n/a
34	POLR2A	chr7:150065057-150067878	HepG2	liver:	n/a	n/a
35	POLR2A	chr7:150064982-150072072	HL-60	blood:	n/a	n/a
36	POLR2A	chr7:150065008-150067946	GM19099	blood:	n/a	n/a
37	POLR2A	chr7:150064898-150068261	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr7:150067688-150068137	IMR90	lung:	n/a	n/a
39	SMC3	chr7:150067704-150068140	HepG2	liver:	n/a	n/a
40	POLR2A	chr7:150067691-150068958	GM12891	blood:	n/a	n/a
41	POLR2A	chr7:150064851-150069341	GM12892	blood:	n/a	n/a
42	WRNIP1	chr7:150066188-150067994	GM12878	blood:	n/a	n/a
43	RCOR1	chr7:150067644-150067951	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150067712-150067762	AG10803	skin:	n/a
2	chr7:150067712-150067762	Jurkat	blood:	n/a
3	chr7:150067712-150067762	GM12891	blood:	n/a
4	chr7:150067712-150067762	HepG2	liver:	n/a
5	chr7:150067712-150067762	HUVEC	blood vessel:	n/a
6	chr7:150067712-150067762	Hepatocyte	liver:	n/a
7	chr7:150067712-150067762	HCPEpiC	choroid plexus:	n/a
8	chr7:150067712-150067762	ovcar-3	ovarian:	n/a
9	chr7:150067712-150067762	AG04450	lung:	fetal
10	chr7:150067712-150067762	GM12878	blood:	n/a
11	chr7:150067712-150067762	SK-N-MC	brain:	n/a
12	chr7:150067712-150067762	ProgFib	skin:	n/a
13	chr7:150067712-150067762	PrEC	prostate:	n/a
14	chr7:150067712-150067762	ECC-1	luminal epithelium:	n/a
15	chr7:150067712-150067762	NHDF-neo	bronchial:	n/a
16	chr7:150067712-150067762	K562	blood:	n/a
17	chr7:150067712-150067762	HL-60	blood:	n/a
18	chr7:150067712-150067762	NH-A	brain:	n/a
19	chr7:150067712-150067762	SK-N-SH	brain:	n/a
20	chr7:150067712-150067762	GM12892	blood:	n/a
21	chr7:150067712-150067762	HCF	heart:	n/a
22	chr7:150067712-150067762	MCF-7	breast:	n/a
23	chr7:150067712-150067762	AoSMC	blood vessel:	n/a
24	chr7:150067712-150067762	HCT-116	colon:	n/a
25	chr7:150067712-150067762	A549	lung:	n/a
26	chr7:150067712-150067762	NB4	blood:	n/a
27	chr7:150067712-150067762	MCF10A-Er-Src	breast:	n/a
28	chr7:150067712-150067762	Caco-2	colon:	n/a
29	chr7:150067712-150067762	BJ	skin:	n/a
30	chr7:150067712-150067762	U87	brain:	n/a
31	chr7:150067712-150067762	NHBE	bronchial:	n/a
32	chr7:150067712-150067762	LNCaP	prostate:	n/a
33	chr7:150067712-150067762	PANC-1	pancreas:	n/a
34	chr7:150067712-150067762	PFSK-1	brain:	n/a
35	chr7:150067712-150067762	HEEpiC	esophagus:	n/a
36	chr7:150067712-150067762	T-47D	breast:	n/a
37	chr7:150067712-150067762	NT2-D1	testis:	n/a
38	chr7:150067712-150067762	AG04449	skin:	fetal
39	chr7:150067712-150067762	CMK	blood:	n/a
40	chr7:150067712-150067762	SKMC	muscle:	n/a
41	chr7:150067712-150067762	HEK293	kidney:	embryo
42	chr7:150067712-150067762	HIPEpiC	eye:	n/a
43	chr7:150067712-150067762	HCM	heart:	n/a
44	chr7:150067712-150067762	BE2_C	brain:	n/a
45	chr7:150067712-150067762	HRCEpiC	kidney:	n/a
46	chr7:150067712-150067762	HRPEpiC	eye:	n/a
47	chr7:150067712-150067762	HPAEpiC	pulmonary alveolar:	n/a
48	chr7:150067712-150067762	AG09309	skin:	n/a
49	chr7:150067712-150067762	AG09319	gingival:	n/a
50	chr7:150067712-150067762	GM19239	blood:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:150063876..150080670-chr7:150093696..150109118,65	MCF-7	breast:
2	chr7:150016171..150021897-chr7:150062899..150068795,19	MCF-7	breast:
3	chr7:150018458..150023402-chr7:150064103..150067772,7	MCF-7	breast:
4	chr7:150066102..150068231-chr7:150757822..150759698,2	MCF-7	breast:
5	chr7:150063752..150069023-chr7:150095376..150104764,21	MCF-7	breast:
6	chr7:150017186..150022141-chr7:150063447..150068849,12	K562	blood:
7	chr7:149570954..149573807-chr7:150065336..150068583,3	MCF-7	breast:
8	chr7:150065484..150068056-chr7:150811875..150813765,2	MCF-7	breast:

No data

Variant related genes	Relation type
REPIN1	TF binding region
REPIN1	CpG island
ENSG00000196456	Chromatin interaction
ENSG00000106526	Chromatin interaction
ENSG00000127399	Chromatin interaction
ENSG00000133612	Chromatin interaction
ENSG00000171130	Chromatin interaction
ENSG00000164889	Chromatin interaction

Extended variants
information (count: 63 )
Associated
traits (count: 15 )

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10248975	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10259796	0.85[CEU][hapmap]
rs10264443	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10271869	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10278277	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10282458	0.90[CEU][hapmap]
rs1047575	0.89[CEU][hapmap]
rs1051760	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1051764	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1051823	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10952250	0.90[CEU][hapmap]
rs10952251	0.87[ASN][1000 genomes]
rs1132261	0.90[CEU][hapmap]
rs11764936	0.90[CEU][hapmap]
rs11769348	0.90[CEU][hapmap]
rs11771677	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11771693	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11972067	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11974980	0.84[MEX][hapmap]
rs17173617	0.84[CEU][hapmap]
rs17173681	0.95[CEU][hapmap]
rs17173682	0.95[CEU][hapmap]
rs1983440	0.90[CEU][hapmap]
rs1983441	0.85[EUR][1000 genomes]
rs28398138	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3735165	0.80[JPT][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3735166	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3735167	0.84[CEU][hapmap]
rs3735169	0.94[CEU][hapmap]
rs3735170	0.94[CEU][hapmap]
rs3735171	0.94[CEU][hapmap]
rs3735172	0.90[CEU][hapmap]
rs3757424	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3757425	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4554381	0.90[CEU][hapmap]
rs6722	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6946097	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6946153	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6964110	0.90[CEU][hapmap]
rs71537958	0.86[EUR][1000 genomes]
rs7800196	0.95[CEU][hapmap];0.90[CHB][hapmap];0.90[JPT][hapmap];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9640161	0.95[CHB][hapmap];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034409	chr7:149844639-150447071	Flanking Active TSS Active TSS Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
2	nsv608990	chr7:149961274-150707488	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
3	nsv1015582	chr7:149967986-150285104	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
4	nsv889453	chr7:150009838-150104410	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers 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	50 gene(s)	inside rSNPs	diseases
5	nsv889454	chr7:150009838-150115183	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
6	nsv889455	chr7:150013393-150104410	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
7	nsv889456	chr7:150013393-150115183	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
8	nsv1017368	chr7:150016952-150655773	Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
9	nsv539195	chr7:150016952-150655773	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
10	nsv889457	chr7:150020295-150104410	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers 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	50 gene(s)	inside rSNPs	diseases
11	nsv889458	chr7:150020295-150115183	Enhancers Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
12	nsv521407	chr7:150020295-150118590	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
13	nsv465211	chr7:150035526-150104410	Flanking Active TSS Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
14	nsv608991	chr7:150035526-150104410	Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
15	nsv889459	chr7:150041610-150071464	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
16	nsv608992	chr7:150045910-150115183	Transcr. at gene 5' and 3' Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
17	esv1819714	chr7:150055837-150154944	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
18	nsv889460	chr7:150060163-150079459	Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers Weak transcription Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
19	nsv889461	chr7:150060163-150081485	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
20	nsv889462	chr7:150060163-150108536	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
21	esv1814724	chr7:150067445-150070663	Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

mRNA abundance (count:15)

SNP	Gene	Cis/trans	Tissue	Source
rs3757423	REPIN1	cis	Muscle Skeletal	GTEx
rs3757423	RARRES2	cis	lymphoblastoid	seeQTL
rs3757423	LRRC61	cis	lymphoblastoid	seeQTL
rs3757423	LRRC61	cis	Thyroid	GTEx
rs3757423	MGC3036	cis	multi-tissue	Pritchard
rs3757423	LRRC61	cis	Muscle Skeletal	GTEx
rs3757423	C7orf29	Cis_1M	lymphoblastoid	RTeQTL
rs3757423	LRRC61	cis	Skin Sun Exposed Lower leg	GTEx
rs3757423	RARRES2	cis	brain	seeQTL
rs3757423	C7orf29	cis	cerebellum	SCAN
rs3757423	LRRC61	cis	cerebellum	SCAN
rs3757423	GIMAP6	cis	cerebellum	SCAN
rs3757423	LRRC61	cis	parietal	SCAN
rs3757423	RARRES2	cis	multi-tissue	Pritchard
rs3757423	C7orf29	cis	lymphoblastoid	seeQTL

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150064600-150067800	Flanking Active TSS	Primary hematopoietic stem cells	blood
2	chr7:150065000-150068400	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr7:150065400-150073600	Transcr. at gene 5' and 3'	Dnd41	blood
4	chr7:150066200-150067800	Flanking Active TSS	Primary B cells from cord blood	blood
5	chr7:150066200-150067800	Flanking Active TSS	Fetal Thymus	thymus
6	chr7:150066200-150068000	Flanking Active TSS	Colonic Mucosa	Colon
7	chr7:150066200-150069200	Transcr. at gene 5' and 3'	Rectal Mucosa Donor 31	rectum
8	chr7:150066400-150067800	Flanking Active TSS	NH-A	brain
9	chr7:150066400-150068400	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
10	chr7:150066400-150068600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr7:150066600-150067800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr7:150066600-150067800	Flanking Active TSS	Brain Cingulate Gyrus	brain
13	chr7:150066600-150067800	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
14	chr7:150066600-150067800	Transcr. at gene 5' and 3'	K562	blood
15	chr7:150066600-150068000	Flanking Active TSS	Osteobl	bone
16	chr7:150066600-150068400	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
17	chr7:150066800-150067800	Transcr. at gene 5' and 3'	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr7:150066800-150067800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr7:150066800-150067800	Flanking Active TSS	Fetal Intestine Large	intestine
20	chr7:150066800-150067800	Enhancers	Placenta Amnion	Placenta Amnion
21	chr7:150066800-150067800	Flanking Active TSS	HSMMtube	muscle
22	chr7:150066800-150067800	Flanking Active TSS	NHLF	lung
23	chr7:150066800-150068000	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr7:150066800-150068000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
25	chr7:150066800-150068000	Flanking Active TSS	Fetal Heart	heart
26	chr7:150066800-150068200	Weak transcription	Aorta	Aorta
27	chr7:150066800-150068200	Transcr. at gene 5' and 3'	Thymus	Thymus
28	chr7:150066800-150068200	Enhancers	HMEC	breast
29	chr7:150066800-150068400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr7:150067000-150067800	Transcr. at gene 5' and 3'	iPS-18 Cell Line	embryonic stem cell
31	chr7:150067000-150067800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
32	chr7:150067000-150068000	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr7:150067000-150068000	Transcr. at gene 5' and 3'	HUES64 Cell Line	embryonic stem cell
34	chr7:150067000-150068000	Transcr. at gene 5' and 3'	iPS-20b Cell Line	embryonic stem cell
35	chr7:150067000-150068000	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
36	chr7:150067000-150068000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
37	chr7:150067000-150068000	Transcr. at gene 5' and 3'	Skeletal Muscle Female	skeletal muscle
38	chr7:150067000-150068000	Transcr. at gene 5' and 3'	A549	lung
39	chr7:150067000-150068000	Transcr. at gene 5' and 3'	Hela-S3	cervix
40	chr7:150067000-150068600	Weak transcription	Ovary	ovary
41	chr7:150067000-150070400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
42	chr7:150067000-150070800	Genic enhancers	Spleen	Spleen
43	chr7:150067200-150067800	Genic enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr7:150067200-150067800	Enhancers	Primary T cells from cord blood	blood
45	chr7:150067200-150067800	Flanking Active TSS	HepG2	liver
46	chr7:150067200-150068000	Enhancers	Primary T cells fromperipheralblood	blood
47	chr7:150067200-150068000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
48	chr7:150067200-150068000	Enhancers	Primary T killer memory cells from peripheral blood	blood
49	chr7:150067200-150068000	Transcr. at gene 5' and 3'	Brain Anterior Caudate	brain
50	chr7:150067200-150068000	Flanking Active TSS	HSMM	muscle

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