Variant report

Variant	rs10156182
Chromosome Location	chr7:40126603-40126604
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 180 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:161)

rs_ID	r²[population]
rs10046564	0.81[CEU][hapmap]
rs10081308	0.88[EUR][1000 genomes]
rs10227386	0.85[CEU][hapmap];0.80[EUR][1000 genomes]
rs10228020	0.80[EUR][1000 genomes]
rs10229517	0.81[EUR][1000 genomes]
rs10230530	0.81[EUR][1000 genomes]
rs10233552	0.93[ASN][1000 genomes]
rs10234693	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10242519	0.80[EUR][1000 genomes]
rs10243494	0.81[EUR][1000 genomes]
rs10243593	0.81[CEU][hapmap]
rs10246466	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1024680	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10252631	0.93[ASN][1000 genomes]
rs10254394	0.96[ASN][1000 genomes]
rs10259565	0.81[EUR][1000 genomes]
rs10261251	0.85[CEU][hapmap];0.81[EUR][1000 genomes]
rs10267954	0.83[EUR][1000 genomes]
rs10268288	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10269349	0.85[CEU][hapmap]
rs10272641	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10275761	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1082028	0.97[EUR][1000 genomes]
rs1082030	0.89[EUR][1000 genomes]
rs10951624	0.97[ASN][1000 genomes]
rs10951625	0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs10951626	0.92[CEU][hapmap]
rs10951627	0.81[CEU][hapmap]
rs11760739	0.85[CEU][hapmap];0.83[EUR][1000 genomes]
rs11763047	0.85[CEU][hapmap];1.00[YRI][hapmap];0.82[EUR][1000 genomes]
rs11767697	0.81[EUR][1000 genomes]
rs11768464	0.81[CEU][hapmap]
rs11768838	0.85[CEU][hapmap]
rs11769327	0.81[EUR][1000 genomes]
rs11972983	0.96[ASN][1000 genomes]
rs11977756	0.80[CHB][hapmap]
rs11980745	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11983287	0.93[ASN][1000 genomes]
rs12333929	0.85[CEU][hapmap]
rs12334141	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12530776	0.83[EUR][1000 genomes]
rs12531761	0.93[ASN][1000 genomes]
rs12531774	0.88[ASN][1000 genomes]
rs12532714	0.80[CHB][hapmap]
rs12533272	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12534074	0.84[CEU][hapmap];0.90[EUR][1000 genomes]
rs12535524	0.84[EUR][1000 genomes]
rs12536190	0.95[ASN][1000 genomes]
rs12536349	0.81[ASN][1000 genomes]
rs12536726	0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs12537125	0.97[ASN][1000 genomes]
rs12537320	0.93[ASN][1000 genomes]
rs1257698	0.93[ASN][1000 genomes]
rs1257699	1.00[CEU][hapmap];0.86[CHB][hapmap];0.97[EUR][1000 genomes]
rs12666454	0.86[ASN][1000 genomes]
rs12669872	0.95[ASN][1000 genomes]
rs13231777	0.85[CEU][hapmap];0.81[EUR][1000 genomes]
rs13239106	0.82[CEU][hapmap]
rs13310449	0.81[CEU][hapmap]
rs1403381	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1406566	0.80[EUR][1000 genomes]
rs1534675	0.90[CEU][hapmap]
rs1568645	0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17171645	0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs17171646	0.93[ASN][1000 genomes]
rs17171658	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs17496429	0.92[ASN][1000 genomes]
rs17496670	0.97[ASN][1000 genomes]
rs17496733	0.94[ASN][1000 genomes]
rs17538125	0.94[ASN][1000 genomes]
rs1874233	0.85[CEU][hapmap];0.92[YRI][hapmap];0.82[EUR][1000 genomes]
rs1881683	0.80[EUR][1000 genomes]
rs1881684	0.83[EUR][1000 genomes]
rs1989589	0.81[EUR][1000 genomes]
rs2015842	0.93[ASN][1000 genomes]
rs2024200	0.85[CEU][hapmap];0.92[YRI][hapmap];0.84[EUR][1000 genomes]
rs2036041	0.82[CEU][hapmap];0.81[EUR][1000 genomes]
rs2052097	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2056775	0.84[CEU][hapmap];0.81[EUR][1000 genomes]
rs2077124	0.96[ASN][1000 genomes]
rs2109339	0.97[ASN][1000 genomes]
rs2109340	0.90[EUR][1000 genomes]
rs2140254	0.80[CEU][hapmap]
rs2159488	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2159489	0.95[ASN][1000 genomes]
rs2302341	0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs2329611	0.82[CEU][hapmap]
rs2329693	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2329695	0.85[CEU][hapmap]
rs28742222	0.89[EUR][1000 genomes]
rs33999222	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3800799	0.90[CHB][hapmap];0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs3800802	0.88[ASN][1000 genomes]
rs3801238	0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs3847019	0.90[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs3847020	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3847021	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3911836	0.93[ASN][1000 genomes]
rs3911889	0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs3966459	0.84[CEU][hapmap]
rs4720347	0.94[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs4720348	0.99[ASN][1000 genomes]
rs4720349	0.97[ASN][1000 genomes]
rs4720352	0.81[ASN][1000 genomes]
rs4720354	0.81[EUR][1000 genomes]
rs4723925	0.88[ASN][1000 genomes]
rs4723927	0.93[ASN][1000 genomes]
rs4723928	0.93[ASN][1000 genomes]
rs4723929	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4723931	0.89[EUR][1000 genomes]
rs6462961	0.85[CEU][hapmap];0.81[EUR][1000 genomes]
rs6462962	0.85[CEU][hapmap]
rs6462963	0.85[CEU][hapmap];0.81[EUR][1000 genomes]
rs6462965	0.81[CEU][hapmap]
rs6944166	0.81[CEU][hapmap]
rs6948982	0.85[CEU][hapmap];0.80[EUR][1000 genomes]
rs6951375	0.85[CEU][hapmap]
rs6952597	0.96[CEU][hapmap];0.95[CHB][hapmap];0.89[JPT][hapmap];0.92[YRI][hapmap];0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6954096	0.85[CEU][hapmap]
rs6957766	0.80[EUR][1000 genomes]
rs6960111	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6962410	0.81[EUR][1000 genomes]
rs6963804	0.90[EUR][1000 genomes]
rs6966917	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6974493	0.92[CEU][hapmap];0.92[YRI][hapmap]
rs6975853	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6979628	0.83[CEU][hapmap];0.81[EUR][1000 genomes]
rs71560176	0.81[EUR][1000 genomes]
rs731847	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs731848	0.96[CEU][hapmap];0.95[CHB][hapmap];0.89[JPT][hapmap];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73394665	0.87[ASN][1000 genomes]
rs758696	0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs773379	0.90[EUR][1000 genomes]
rs773381	0.91[EUR][1000 genomes]
rs773382	0.82[CEU][hapmap]
rs773385	0.97[EUR][1000 genomes]
rs773386	0.97[EUR][1000 genomes]
rs773393	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs773397	0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs773402	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs773403	0.97[EUR][1000 genomes]
rs773410	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs773411	0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs773413	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs773414	0.97[EUR][1000 genomes]
rs773415	0.89[EUR][1000 genomes]
rs773424	1.00[CEU][hapmap];0.85[CHB][hapmap];0.97[EUR][1000 genomes]
rs7776964	0.81[EUR][1000 genomes]
rs7778061	0.81[EUR][1000 genomes]
rs7779663	0.94[ASN][1000 genomes]
rs7780858	0.81[EUR][1000 genomes]
rs7796371	0.80[EUR][1000 genomes]
rs7797041	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.89[AFR][1000 genomes];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7799846	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.82[AFR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7802584	0.81[EUR][1000 genomes]
rs7808529	0.85[CEU][hapmap];0.80[EUR][1000 genomes]
rs7810509	0.89[EUR][1000 genomes]
rs887445	0.81[EUR][1000 genomes]
rs887447	0.88[CEU][hapmap];0.81[EUR][1000 genomes]
rs9639818	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9690188	0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	nsv464437	chr7:40094641-40197168	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
17	nsv606709	chr7:40094641-40197168	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
18	nsv1032278	chr7:40097371-40396300	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS 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
19	nsv887982	chr7:40098787-40193535	Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:40028000-40127800	Weak transcription	Colonic Mucosa	Colon
2	chr7:40043600-40127800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr7:40055800-40127600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr7:40055800-40127600	Weak transcription	Rectal Smooth Muscle	rectum
5	chr7:40056200-40128600	Weak transcription	A549	lung
6	chr7:40058600-40126800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr7:40072000-40130400	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr7:40077200-40127800	Weak transcription	Esophagus	oesophagus
9	chr7:40080200-40132400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr7:40082000-40127800	Weak transcription	Pancreas	Pancrea
11	chr7:40082600-40128200	Weak transcription	Spleen	Spleen
12	chr7:40083400-40127400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
13	chr7:40086400-40127800	Weak transcription	Thymus	Thymus
14	chr7:40092600-40127600	Weak transcription	Brain Substantia Nigra	brain
15	chr7:40093800-40127600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr7:40094800-40127800	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr7:40095800-40127800	Weak transcription	Fetal Brain Female	brain
18	chr7:40097200-40127600	Weak transcription	HSMMtube	muscle
19	chr7:40097200-40132600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr7:40097200-40132600	Weak transcription	Right Ventricle	heart
21	chr7:40098200-40132400	Weak transcription	Psoas Muscle	Psoas
22	chr7:40098600-40127600	Weak transcription	Brain Hippocampus Middle	brain
23	chr7:40099800-40132600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr7:40103000-40127600	Weak transcription	Stomach Smooth Muscle	stomach
25	chr7:40103000-40127600	Weak transcription	NHEK	skin
26	chr7:40103000-40131400	Weak transcription	NHLF	lung
27	chr7:40103200-40126800	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr7:40104400-40127600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr7:40106000-40127600	Weak transcription	Hela-S3	cervix
30	chr7:40106000-40127800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr7:40106000-40131400	Weak transcription	HMEC	breast
32	chr7:40106800-40127800	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr7:40107000-40127800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
34	chr7:40112600-40127800	Weak transcription	HepG2	liver
35	chr7:40116000-40127400	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr7:40116400-40136000	Weak transcription	Fetal Brain Male	brain
37	chr7:40117600-40138000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr7:40118000-40127800	Weak transcription	Colon Smooth Muscle	Colon
39	chr7:40118200-40126800	Weak transcription	Primary neutrophils fromperipheralblood	blood
40	chr7:40118600-40136600	Strong transcription	Primary monocytes fromperipheralblood	blood
41	chr7:40119400-40127800	Weak transcription	Fetal Lung	lung
42	chr7:40119600-40127800	Weak transcription	Brain Germinal Matrix	brain
43	chr7:40119600-40132600	Weak transcription	Small Intestine	intestine
44	chr7:40119800-40127600	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr7:40119800-40135600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr7:40120000-40127400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr7:40120200-40127400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr7:40120200-40127800	Weak transcription	Brain Anterior Caudate	brain
49	chr7:40120400-40126800	Weak transcription	Osteobl	bone
50	chr7:40120400-40127800	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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