Variant report

Variant	rs1051764
Chromosome Location	chr7:150070663-150070664
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:58)
CpG islands
(count:0)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:58 , 50 per page) page: 1 2

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	chr7:150070092-150070802	HepG2	liver:	n/a	n/a
3	POLR2A	chr7:150069798-150072038	GM12878	blood:	n/a	n/a
4	MAZ	chr7:150070653-150070797	GM12878	blood:	n/a	n/a
5	POLR2A	chr7:150069962-150070969	K562	blood:	n/a	n/a
6	POLR2A	chr7:150069346-150072105	GM12892	blood:	n/a	n/a
7	MAZ	chr7:150070573-150070921	K562	blood:	n/a	n/a
8	POLR2A	chr7:150069466-150070970	GM12878	blood:	n/a	n/a
9	YY1	chr7:150070639-150070919	K562	blood:	n/a	n/a
10	RCOR1	chr7:150070465-150070858	GM12878	blood:	n/a	n/a
11	USF2	chr7:150070607-150070759	GM12878	blood:	n/a	n/a
12	POLR2A	chr7:150069579-150070974	K562	blood:	n/a	n/a
13	POLR2A	chr7:150065010-150072093	GM12878	blood:	n/a	n/a
14	RCOR1	chr7:150070648-150070919	K562	blood:	n/a	n/a
15	POLR2A	chr7:150070641-150070952	ECC-1	luminal epithelium:	n/a	n/a
16	TBL1XR1	chr7:150070575-150070862	K562	blood:	n/a	n/a
17	POLR2A	chr7:150070179-150070992	GM19099	blood:	n/a	n/a
18	POLR2A	chr7:150065044-150070916	GM19193	blood:	n/a	n/a
19	POLR2A	chr7:150070405-150070946	H1-hESC	embryonic stem cell:	n/a	n/a
20	POLR2A	chr7:150070139-150070730	Hela-S3	cervix:	n/a	n/a
21	POLR2A	chr7:150070004-150070724	A549	lung:	n/a	n/a
22	POLR2A	chr7:150064968-150071009	K562	blood:	n/a	n/a
23	POLR2A	chr7:150070458-150070897	GM12878	blood:	n/a	n/a
24	POLR2A	chr7:150069743-150070753	PANC-1	pancreas:	n/a	n/a
25	POLR2A	chr7:150068924-150072074	HL-60	blood:	n/a	n/a
26	POLR2A	chr7:150069942-150070992	GM12891	blood:	n/a	n/a
27	SPI1	chr7:150070657-150070994	GM12878	blood:	n/a	n/a
28	POLR2A	chr7:150069990-150071018	K562	blood:	n/a	n/a
29	POLR2A	chr7:150068187-150072706	Hela-S3	cervix:	n/a	n/a
30	POLR2A	chr7:150069604-150071006	GM12891	blood:	n/a	n/a
31	POLR2A	chr7:150065009-150070940	GM18505	blood:	n/a	n/a
32	POLR2A	chr7:150069727-150071177	GM12878	blood:	n/a	n/a
33	POLR2A	chr7:150070645-150070845	HepG2	liver:	n/a	n/a
34	POLR2A	chr7:150064952-150072087	GM12892	blood:	n/a	n/a
35	POLR2A	chr7:150069785-150070972	K562	blood:	n/a	n/a
36	ZMIZ1	chr7:150070623-150070835	K562	blood:	n/a	n/a
37	ELF1	chr7:150070648-150070970	K562	blood:	n/a	n/a
38	POLR2A	chr7:150070459-150071056	GM12878	blood:	n/a	n/a
39	POLR2A	chr7:150069494-150072013	HepG2	liver:	n/a	n/a
40	POLR2A	chr7:150064843-150076606	K562	blood:	n/a	n/a
41	POLR2A	chr7:150070439-150070758	MCF-7	breast:	n/a	n/a
42	POLR2A	chr7:150069673-150072066	GM12892	blood:	n/a	n/a
43	RAD21	chr7:150070632-150070820	K562	blood:	n/a	n/a
44	CBX3	chr7:150070516-150070994	K562	blood:	n/a	n/a
45	NR2F2	chr7:150070435-150071301	K562	blood:	n/a	n/a
46	TEAD4	chr7:150070503-150070955	K562	blood:	n/a	n/a
47	ZBTB7A	chr7:150070662-150070869	K562	blood:	n/a	n/a
48	POLR2A	chr7:150064982-150072072	HL-60	blood:	n/a	n/a
49	POLR2A	chr7:150069477-150071032	GM12891	blood:	n/a	n/a
50	POLR2A	chr7:150069643-150070742	H1-hESC	embryonic stem cell:	n/a	n/a

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:150063876..150080670-chr7:150093696..150109118,65	MCF-7	breast:
2	chr7:149552909..149554975-chr7:150070039..150072542,2	MCF-7	breast:
3	chr7:150019286..150021465-chr7:150069323..150073240,4	MCF-7	breast:
4	chr7:150026034..150028099-chr7:150070313..150072987,2	K562	blood:
5	chr7:150019550..150021994-chr7:150069161..150070677,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000240449	TF binding region
ENSG00000106479	Chromatin interaction
ENSG00000127399	Chromatin interaction
ENSG00000106526	Chromatin interaction
ENSG00000188707	Chromatin interaction
ENSG00000196456	Chromatin interaction

Extended variants
information (count: 62 )
Associated
traits (count: 15 )

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10248975	0.80[AMR][1000 genomes];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	0.86[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];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];0.90[MEX][hapmap];0.92[MKK][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];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[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	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
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	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3735165	0.80[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3735166	0.88[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]
rs3757423	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]
rs3757424	0.94[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];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4554381	0.90[CEU][hapmap]
rs6722	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6946097	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs6946153	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
rs1051764	C7orf29	cis	Lymphoblastoid	GTEx
rs1051764	RARRES2	cis	lymphoblastoid	seeQTL
rs1051764	LRRC61	cis	Muscle Skeletal	GTEx
rs1051764	C7orf29	cis	lymphoblastoid	seeQTL
rs1051764	REPIN1	cis	Muscle Skeletal	GTEx
rs1051764	RARRES2	cis	multi-tissue	Pritchard
rs1051764	C7orf29	Cis_1M	lymphoblastoid	RTeQTL
rs1051764	LRRC61	cis	cerebellum	SCAN
rs1051764		cis	Lymphoblastoid	GTEx
rs1051764	LRRC61	cis	lymphoblastoid	seeQTL
rs1051764	LRRC61	cis	Thyroid	GTEx
rs1051764	LRRC61	cis	Skin Sun Exposed Lower leg	GTEx
rs1051764	C7orf29	cis	cerebellum	SCAN
rs1051764	ZBED6CL	cis	Esophagus Muscularis	GTEx
rs1051764	LRRC61	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150065400-150073600	Transcr. at gene 5' and 3'	Dnd41	blood
2	chr7:150067000-150070800	Genic enhancers	Spleen	Spleen
3	chr7:150067200-150071000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr7:150067200-150072000	Transcr. at gene 5' and 3'	Rectal Mucosa Donor 29	rectum
5	chr7:150067400-150071200	Genic enhancers	Right Ventricle	heart
6	chr7:150067400-150071400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr7:150067400-150072000	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr7:150067600-150070800	Genic enhancers	Gastric	stomach
9	chr7:150067600-150070800	Genic enhancers	Stomach Smooth Muscle	stomach
10	chr7:150067600-150071600	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr7:150067600-150071800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr7:150067600-150071800	Genic enhancers	Liver	Liver
13	chr7:150067600-150072000	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr7:150067600-150072000	Genic enhancers	Pancreas	Pancrea
15	chr7:150067800-150071200	Strong transcription	HUES48 Cell Line	embryonic stem cell
16	chr7:150067800-150071400	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr7:150067800-150071800	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr7:150067800-150071800	Strong transcription	Primary monocytes fromperipheralblood	blood
19	chr7:150067800-150072000	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr7:150068000-150070800	Transcr. at gene 5' and 3'	Colonic Mucosa	Colon
21	chr7:150068000-150071600	Strong transcription	HUES64 Cell Line	embryonic stem cell
22	chr7:150068000-150071800	Strong transcription	H9 Cell Line	embryonic stem cell
23	chr7:150068000-150072000	Strong transcription	Cortex derived primary cultured neurospheres	brain
24	chr7:150068000-150072000	Enhancers	Fetal Heart	heart
25	chr7:150068000-150072000	Strong transcription	A549	lung
26	chr7:150068000-150073000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr7:150068000-150073000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
28	chr7:150068000-150073000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr7:150068200-150071400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
30	chr7:150068200-150071600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr7:150068200-150071800	Strong transcription	Monocytes-CD14+_RO01746	blood
32	chr7:150068200-150072000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr7:150068200-150073400	Weak transcription	Fetal Kidney	kidney
34	chr7:150068200-150075400	Weak transcription	HMEC	breast
35	chr7:150068400-150071200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr7:150068400-150071200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr7:150068400-150071800	Strong transcription	Osteobl	bone
38	chr7:150068400-150074000	Genic enhancers	Fetal Intestine Small	intestine
39	chr7:150068600-150071600	Strong transcription	HUVEC	blood vessel
40	chr7:150068600-150072000	Strong transcription	NHLF	lung
41	chr7:150068800-150071200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr7:150068800-150072000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr7:150068800-150072400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr7:150068800-150075200	Weak transcription	NH-A	brain
45	chr7:150069000-150072000	Strong transcription	Brain Germinal Matrix	brain
46	chr7:150069000-150075200	Weak transcription	Fetal Brain Male	brain
47	chr7:150069200-150072200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr7:150069400-150071000	Transcr. at gene 5' and 3'	Rectal Mucosa Donor 31	rectum
49	chr7:150069400-150071800	Strong transcription	HSMMtube	muscle
50	chr7:150069600-150071200	Strong transcription	Primary T helper cells fromperipheralblood	blood

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