Variant report

Variant	rs10272641
Chromosome Location	chr7:40089932-40089933
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:39987621..39991955-chr7:40089379..40093722,6	MCF-7	breast:
2	chr7:39989128..39990851-chr7:40089712..40092117,2	K562	blood:
3	chr7:39988782..39993568-chr7:40089798..40094373,7	MCF-7	breast:

Variant related genes	Relation type
ENSG00000065883	Chromatin interaction
ENSG00000259826	Chromatin interaction

Extended variants
information (count: 166 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:148)

rs_ID	r²[population]
rs10046564	0.81[CEU][hapmap]
rs10081308	0.87[EUR][1000 genomes]
rs10156182	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10227386	0.84[CEU][hapmap]
rs10233552	0.95[ASN][1000 genomes]
rs10234693	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10243494	0.80[EUR][1000 genomes]
rs10243593	0.81[CEU][hapmap]
rs10246466	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1024680	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10252631	0.95[ASN][1000 genomes]
rs10254394	0.94[ASN][1000 genomes]
rs10259565	0.80[EUR][1000 genomes]
rs10261251	0.84[CEU][hapmap]
rs10267954	0.82[EUR][1000 genomes]
rs10268288	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10269349	0.85[CEU][hapmap];0.83[MEX][hapmap]
rs10275761	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1082028	0.96[EUR][1000 genomes]
rs1082030	0.88[EUR][1000 genomes]
rs10951624	0.95[ASN][1000 genomes]
rs10951625	0.95[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs10951626	0.92[CEU][hapmap]
rs10951627	0.81[CEU][hapmap]
rs11760739	0.85[CEU][hapmap];0.82[EUR][1000 genomes]
rs11763047	0.85[CEU][hapmap];0.81[EUR][1000 genomes]
rs11767697	0.80[EUR][1000 genomes]
rs11768464	0.81[CEU][hapmap]
rs11768838	0.85[CEU][hapmap]
rs11769327	0.80[EUR][1000 genomes]
rs11972983	0.94[ASN][1000 genomes]
rs11980745	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11983287	0.95[ASN][1000 genomes]
rs12333929	0.85[CEU][hapmap];0.88[MEX][hapmap]
rs12334141	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12530776	0.82[EUR][1000 genomes]
rs12531761	0.95[ASN][1000 genomes]
rs12531774	0.90[ASN][1000 genomes]
rs12533272	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12534074	0.84[CEU][hapmap];0.83[MEX][hapmap];0.86[TSI][hapmap];0.89[EUR][1000 genomes]
rs12535524	0.83[EUR][1000 genomes]
rs12536190	0.93[ASN][1000 genomes]
rs12536726	0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs12537125	0.95[ASN][1000 genomes]
rs12537320	0.92[ASN][1000 genomes]
rs1257698	0.95[ASN][1000 genomes]
rs1257699	1.00[CEU][hapmap];0.85[CHB][hapmap];0.96[EUR][1000 genomes]
rs12666454	0.85[ASN][1000 genomes]
rs12669872	0.93[ASN][1000 genomes]
rs13231777	0.85[CEU][hapmap];0.83[MEX][hapmap];0.80[EUR][1000 genomes]
rs13239106	0.81[CEU][hapmap]
rs13310449	0.81[CEU][hapmap]
rs1403381	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1534675	0.89[CEU][hapmap]
rs1568645	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17171637	0.90[CHD][hapmap]
rs17171645	0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs17171646	0.95[ASN][1000 genomes]
rs17171658	0.96[CEU][hapmap];0.95[CHB][hapmap];0.92[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.89[TSI][hapmap]
rs17496429	0.93[ASN][1000 genomes]
rs17496670	0.95[ASN][1000 genomes]
rs17496733	0.93[ASN][1000 genomes]
rs17538125	0.96[ASN][1000 genomes]
rs1874233	0.84[CEU][hapmap];0.82[EUR][1000 genomes]
rs1881684	0.82[EUR][1000 genomes]
rs1989589	0.80[EUR][1000 genomes]
rs2015842	0.92[ASN][1000 genomes]
rs2024200	0.85[CEU][hapmap];0.88[MEX][hapmap];0.83[EUR][1000 genomes]
rs2036041	0.81[CEU][hapmap]
rs2052097	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2056775	0.84[CEU][hapmap];0.88[MEX][hapmap];0.80[EUR][1000 genomes]
rs2077124	0.94[ASN][1000 genomes]
rs2109339	0.96[ASN][1000 genomes]
rs2109340	0.89[EUR][1000 genomes]
rs2159488	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2159489	0.97[ASN][1000 genomes]
rs2302341	0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2329611	0.81[CEU][hapmap]
rs2329693	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2329695	0.85[CEU][hapmap];0.88[MEX][hapmap]
rs28742222	0.88[EUR][1000 genomes]
rs33999222	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3800799	0.95[CHB][hapmap];0.95[CHD][hapmap];0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs3800802	0.89[ASN][1000 genomes]
rs3801238	0.95[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs3847019	0.90[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs3847020	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3847021	0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3911836	0.92[ASN][1000 genomes]
rs3911889	0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs3966459	0.84[CEU][hapmap]
rs4720347	0.94[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs4720348	0.97[ASN][1000 genomes]
rs4720349	0.95[ASN][1000 genomes]
rs4720354	0.80[EUR][1000 genomes]
rs4723925	0.90[ASN][1000 genomes]
rs4723927	0.95[ASN][1000 genomes]
rs4723928	0.95[ASN][1000 genomes]
rs4723929	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4723931	0.88[EUR][1000 genomes]
rs6462961	0.84[CEU][hapmap];0.80[EUR][1000 genomes]
rs6462962	0.85[CEU][hapmap];0.83[MEX][hapmap]
rs6462963	0.85[CEU][hapmap];0.83[MEX][hapmap];0.80[EUR][1000 genomes]
rs6462965	0.81[CEU][hapmap];0.88[MEX][hapmap]
rs6944166	0.81[CEU][hapmap];0.83[MEX][hapmap]
rs6948982	0.85[CEU][hapmap]
rs6951375	0.85[CEU][hapmap]
rs6952597	0.96[CEU][hapmap];0.95[CHB][hapmap];0.87[CHD][hapmap];0.93[GIH][hapmap];0.89[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6954096	0.85[CEU][hapmap];0.83[MEX][hapmap]
rs6960111	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6962410	0.80[EUR][1000 genomes]
rs6963804	0.89[EUR][1000 genomes]
rs6966917	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6974493	0.92[CEU][hapmap];0.81[TSI][hapmap]
rs6975853	0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6979628	0.83[CEU][hapmap];0.80[EUR][1000 genomes]
rs71560176	0.80[EUR][1000 genomes]
rs731847	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs731848	1.00[ASW][hapmap];0.96[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];0.93[GIH][hapmap];0.90[JPT][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];0.90[YRI][hapmap];0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73394665	0.85[ASN][1000 genomes]
rs758696	0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs773379	0.89[EUR][1000 genomes]
rs773381	0.90[EUR][1000 genomes]
rs773382	0.81[CEU][hapmap]
rs773385	0.96[EUR][1000 genomes]
rs773386	0.96[EUR][1000 genomes]
rs773393	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap];0.90[YRI][hapmap];0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs773397	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs773402	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs773403	0.96[EUR][1000 genomes]
rs773410	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs773411	0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs773413	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs773414	0.96[EUR][1000 genomes]
rs773415	0.88[EUR][1000 genomes]
rs773424	1.00[CEU][hapmap];0.85[CHB][hapmap];0.92[CHD][hapmap];0.98[GIH][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.96[EUR][1000 genomes]
rs7776964	0.80[EUR][1000 genomes]
rs7779663	0.93[ASN][1000 genomes]
rs7780858	0.80[EUR][1000 genomes]
rs7797041	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7799846	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7802584	0.80[EUR][1000 genomes]
rs7808529	0.85[CEU][hapmap]
rs7810509	0.88[EUR][1000 genomes]
rs887445	0.80[EUR][1000 genomes]
rs887447	0.88[CEU][hapmap];0.80[EUR][1000 genomes]
rs9639818	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9690188	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv887973	chr7:39772654-40110720	Strong transcription Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	58 gene(s)	inside rSNPs	diseases
2	nsv887975	chr7:39858378-40124137	Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
3	nsv1015322	chr7:40006195-40141195	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	esv2761319	chr7:40006195-40142139	Strong transcription Enhancers Weak transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
5	nsv464436	chr7:40018693-40133044	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv606706	chr7:40018693-40133044	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
7	nsv606707	chr7:40021044-40133044	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	nsv606708	chr7:40021044-40157040	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
9	nsv887978	chr7:40030488-40124137	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
10	nsv429748	chr7:40054760-40140660	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
11	esv2756801	chr7:40060180-40269583	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
12	esv2759525	chr7:40060180-40269583	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
13	nsv887979	chr7:40067021-40193535	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
14	nsv887980	chr7:40067021-40203356	Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
15	nsv887981	chr7:40075461-40203356	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
16	nsv971193	chr7:40075881-40197955	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
17	esv34547	chr7:40077032-40230965	Strong transcription Enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
18	nsv824080	chr7:40077089-40198644	Weak transcription Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs10272641	CDK13	cis	lymphoblastoid	seeQTL
rs10272641	C7orf36	cis	parietal	SCAN

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:40026600-40096800	Weak transcription	Right Ventricle	heart
2	chr7:40028000-40127800	Weak transcription	Colonic Mucosa	Colon
3	chr7:40043600-40095200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr7:40043600-40127800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr7:40044400-40096000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr7:40047600-40102600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr7:40048000-40102400	Weak transcription	HMEC	breast
8	chr7:40048000-40102400	Weak transcription	NHEK	skin
9	chr7:40049000-40096200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr7:40055600-40126400	Weak transcription	Aorta	Aorta
11	chr7:40055800-40092200	Weak transcription	Colon Smooth Muscle	Colon
12	chr7:40055800-40097000	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr7:40055800-40102400	Weak transcription	NHLF	lung
14	chr7:40055800-40110000	Weak transcription	Gastric	stomach
15	chr7:40055800-40127600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr7:40055800-40127600	Weak transcription	Rectal Smooth Muscle	rectum
17	chr7:40056000-40092200	Weak transcription	Brain Substantia Nigra	brain
18	chr7:40056000-40097000	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr7:40056000-40097800	Weak transcription	Brain Hippocampus Middle	brain
20	chr7:40056000-40097800	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr7:40056000-40105400	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr7:40056000-40112200	Weak transcription	HepG2	liver
23	chr7:40056200-40128600	Weak transcription	A549	lung
24	chr7:40058400-40101800	Weak transcription	Fetal Brain Male	brain
25	chr7:40058600-40126800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr7:40059000-40125200	Weak transcription	Fetal Kidney	kidney
27	chr7:40059400-40092800	Weak transcription	HSMMtube	muscle
28	chr7:40060200-40102400	Weak transcription	NHDF-Ad	bronchial
29	chr7:40060400-40098800	Weak transcription	Brain Anterior Caudate	brain
30	chr7:40067400-40096000	Weak transcription	NH-A	brain
31	chr7:40067600-40096800	Weak transcription	Left Ventricle	heart
32	chr7:40067800-40095600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr7:40070600-40104000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr7:40072000-40096000	Weak transcription	Stomach Smooth Muscle	stomach
35	chr7:40072000-40098800	Weak transcription	Ovary	ovary
36	chr7:40072000-40104000	Weak transcription	Duodenum Mucosa	Duodenum
37	chr7:40072000-40130400	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr7:40072600-40101000	Weak transcription	Primary hematopoietic stem cells	blood
39	chr7:40074000-40097000	Weak transcription	Right Atrium	heart
40	chr7:40074000-40102600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
41	chr7:40074600-40097000	Weak transcription	Adipose Nuclei	Adipose
42	chr7:40075200-40092400	Weak transcription	Dnd41	blood
43	chr7:40075200-40093200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr7:40075200-40096000	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr7:40075800-40096600	Weak transcription	Lung	lung
46	chr7:40075800-40102400	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr7:40076200-40102400	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr7:40076200-40106800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr7:40076400-40096000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr7:40077200-40098800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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