Variant report

Variant	nsv1031309
Chromosome Location	chr7:150171651-150222230
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:184)
CpG islands
(count:1282)
Chromatin interactive
region (count:8)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:184 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:150214006-150214042	K562	blood:	n/a	n/a
2	BHLHE40	chr7:150174446-150174521	K562	blood:	n/a	n/a
3	BRCA1	chr7:150212081-150212213	GM12878	blood:	n/a	n/a
4	CBX3	chr7:150174282-150174708	K562	blood:	n/a	n/a
5	CBX3	chr7:150174152-150174771	K562	blood:	n/a	n/a
6	CEBPB	chr7:150174473-150174613	K562	blood:	n/a	n/a
7	CHD1	chr7:150212027-150212511	GM12878	blood:	n/a	n/a
8	CTCF	chr7:150221240-150221390	GM06990	blood:	n/a	n/a
9	CTCF	chr7:150187425-150187463	GM10248	blood:	n/a	n/a
10	CTCF	chr7:150220083-150220229	Lung_OC	lung:	n/a	n/a
11	CTCF	chr7:150188931-150188975	Pancreas_OC	pancreas:	n/a	n/a
12	CTCF	chr7:150201060-150201210	GM12873	blood:	n/a	n/a
13	CTCF	chr7:150182037-150182045	GM10266	blood:	n/a	n/a
14	CTCF	chr7:150221260-150221410	HepG2	liver:	n/a	n/a
15	CTCF	chr7:150221320-150221348	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr7:150209790-150209854	GM13976	blood:	n/a	n/a
17	CTCF	chr7:150221200-150221350	GM12875	blood:	n/a	n/a
18	CTCF	chr7:150221280-150221430	GM12873	blood:	n/a	n/a
19	CTCF	chr7:150221240-150221390	GM12866	blood:	n/a	n/a
20	CTCF	chr7:150221260-150221410	GM12864	blood:	n/a	n/a
21	CTCF	chr7:150211900-150212050	GM12864	blood:	n/a	n/a
22	CTCF	chr7:150175200-150175350	GM12867	blood:	n/a	n/a
23	CTCF	chr7:150221125-150221401	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr7:150212020-150212170	GM12875	blood:	n/a	n/a
25	CTCF	chr7:150197166-150197218	LNCaP	prostate:	n/a	n/a
26	CUX1	chr7:150174420-150174584	K562	blood:	n/a	n/a
27	CUX1	chr7:150174075-150174080	K562	blood:	n/a	n/a
28	E2F4	chr7:150219047-150219110	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F4	chr7:150215187-150215560	MCF10A-Er-Src	breast:	n/a	n/a
30	EGR1	chr7:150174493-150174722	K562	blood:	n/a	n/a
31	EGR1	chr7:150174521-150174789	K562	blood:	n/a	n/a
32	ELF1	chr7:150174299-150174804	K562	blood:	n/a	n/a
33	EP300	chr7:150174503-150174687	K562	blood:	n/a	n/a
34	FOS	chr7:150176115-150176673	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr7:150213926-150214680	HUVEC	blood vessel:	n/a	chr7:150214252-150214263
36	FOS	chr7:150176162-150176627	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr7:150183163-150183515	HUVEC	blood vessel:	n/a	chr7:150183363-150183374
38	FOS	chr7:150173353-150173679	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr7:150175983-150176677	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr7:150214132-150214400	MCF10A-Er-Src	breast:	n/a	chr7:150214252-150214263
41	FOS	chr7:150176178-150176579	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr7:150173404-150173747	MCF10A-Er-Src	breast:	n/a	n/a
43	FOXA1	chr7:150173976-150174165	HepG2	liver:	n/a	chr7:150174076-150174091
44	FOXA2	chr7:150173918-150174126	HepG2	liver:	n/a	n/a
45	GABPA	chr7:150174306-150174713	K562	blood:	n/a	n/a
46	GABPA	chr7:150174463-150174714	K562	blood:	n/a	n/a
47	GATA2	chr7:150180802-150181606	HUVEC	blood vessel:	n/a	chr7:150181074-150181083 chr7:150181294-150181305
48	GATA2	chr7:150202896-150203094	K562	blood:	n/a	n/a
49	GATA3	chr7:150216101-150216239	SH-SY5Y	brain:	n/a	n/a
50	HCFC1	chr7:150174534-150174547	K562	blood:	n/a	n/a

(count:1282 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150211855-150211905	ovcar-3	ovarian:	n/a
2	chr7:150211855-150211905	ovcar-3	ovarian:	n/a
3	chr7:150211855-150211905	LNCaP	prostate:	n/a
4	chr7:150210785-150210835	HPAEpiC	pulmonary alveolar:	n/a
5	chr7:150210980-150211030	HRPEpiC	eye:	n/a
6	chr7:150216489-150216539	HRE	kidney:	n/a
7	chr7:150216489-150216539	NT2-D1	testis:	n/a
8	chr7:150174632-150174682	HCF	heart:	n/a
9	chr7:150211855-150211905	HCPEpiC	choroid plexus:	n/a
10	chr7:150174632-150174682	BJ	skin:	n/a
11	chr7:150217030-150217080	LNCaP	prostate:	n/a
12	chr7:150212707-150212757	AoSMC	blood vessel:	n/a
13	chr7:150210980-150211030	SK-N-SH_RA	brain:	n/a
14	chr7:150216489-150216539	PANC-1	pancreas:	n/a
15	chr7:150217030-150217080	HL-60	blood:	n/a
16	chr7:150217056-150217106	MCF10A-Er-Src	breast:	n/a
17	chr7:150174540-150174590	CMK	blood:	n/a
18	chr7:150217030-150217080	HPAEpiC	pulmonary alveolar:	n/a
19	chr7:150211939-150211989	LNCaP	prostate:	n/a
20	chr7:150174540-150174590	U87	brain:	n/a
21	chr7:150216872-150216922	HAEpiC	amniotic membrane:	n/a
22	chr7:150174507-150174557	ovcar-3	ovarian:	n/a
23	chr7:150217030-150217080	SK-N-MC	brain:	n/a
24	chr7:150211761-150211811	HCT-116	colon:	n/a
25	chr7:150210785-150210835	HMEC	breast:	n/a
26	chr7:150211152-150211202	HepG2	liver:	n/a
27	chr7:150174507-150174557	GM12892	blood:	n/a
28	chr7:150211855-150211905	HNPCEpiC	eye:	n/a
29	chr7:150210785-150210835	RPTEC	kidney:	n/a
30	chr7:150210980-150211030	NHDF-neo	bronchial:	n/a
31	chr7:150211152-150211202	GM12892	blood:	n/a
32	chr7:150174540-150174590	ovcar-3	ovarian:	n/a
33	chr7:150211811-150211861	HCT-116	colon:	n/a
34	chr7:150216872-150216922	U87	brain:	n/a
35	chr7:150175800-150175850	PANC-1	pancreas:	n/a
36	chr7:150174632-150174682	IMR90	lung:	fetal
37	chr7:150216489-150216539	GM19239	blood:	n/a
38	chr7:150216872-150216922	HCF	heart:	n/a
39	chr7:150211152-150211202	ovcar-3	ovarian:	n/a
40	chr7:150174507-150174557	HPAEpiC	pulmonary alveolar:	n/a
41	chr7:150174507-150174557	ProgFib	skin:	n/a
42	chr7:150217056-150217106	IMR90	lung:	fetal
43	chr7:150217081-150217131	SAEC	small airway:	n/a
44	chr7:150217056-150217106	GM06990	blood:	n/a
45	chr7:150217056-150217106	HRCEpiC	kidney:	n/a
46	chr7:150211152-150211202	AoSMC	blood vessel:	n/a
47	chr7:150217056-150217106	BJ	skin:	n/a
48	chr7:150174507-150174557	MCF-7	breast:	n/a
49	chr7:150211820-150211870	ProgFib	skin:	n/a
50	chr7:150174632-150174682	PANC-1	pancreas:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:150208954..150212624-chr7:150214367..150216129,3	K562	blood:
2	chr7:150168329..150170733-chr7:150189795..150191535,2	K562	blood:
3	chr7:150172387..150174291-chr7:150178480..150181498,3	K562	blood:
4	chr7:150168756..150171646-chr7:150175506..150177582,2	MCF-7	breast:
5	chr7:150029707..150031662-chr7:150170902..150172966,2	K562	blood:
6	chr7:150221183..150223870-chr7:150226440..150228746,2	K562	blood:
7	chr7:150172387..150174291-chr7:150178480..150181498,3	K562	blood:
8	chr7:150164063..150168544-chr7:150171397..150173219,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GIMAP6-5	chr7:150181149-150182223	NONHSAT124141
2	lnc-GIMAP6-4	chr7:150209647-150210927	NONHSAT124142

No data

Variant related genes	Relation type
ENSG00000271582	TF binding region
GIMAP7	TF binding region
STRADBP1	TF binding region
ENSG00000271582	CpG island
GIMAP7	CpG island
STRADBP1	CpG island
ENSG00000213205	chromatin interactions
ENSG00000179144	chromatin interactions

Extended variants
information (count: 2325 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:2325 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549450438	chr7:150171652-150171653	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs149276246	chr7:150171653-150171654	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs190925921	chr7:150171656-150171657	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs376570927	chr7:150171686-150171687	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs60114833	chr7:150171710-150171711	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs201613876	chr7:150171719-150171720	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs534907419	chr7:150171732-150171733	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs567749757	chr7:150171807-150171808	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs183254857	chr7:150171810-150171811	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs367882588	chr7:150171815-150171816	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs566253011	chr7:150171816-150171817	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577888139	chr7:150171824-150171825	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs374108635	chr7:150171837-150171838	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs71537965	chr7:150171901-150171902	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs186347968	chr7:150171936-150171937	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs190469485	chr7:150171969-150171970	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs562074568	chr7:150171974-150171975	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs183084956	chr7:150172036-150172037	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs187778850	chr7:150172041-150172042	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564474941	chr7:150172058-150172059	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs148567867	chr7:150172102-150172103	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs549933416	chr7:150172139-150172140	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs59777480	chr7:150172160-150172161	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs146647087	chr7:150172178-150172179	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs548843288	chr7:150172190-150172191	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs116283182	chr7:150172194-150172195	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs534628201	chr7:150172246-150172247	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs368725858	chr7:150172263-150172264	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs192449115	chr7:150172273-150172274	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs140021553	chr7:150172349-150172350	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs184038264	chr7:150172425-150172426	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs117489378	chr7:150172426-150172427	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs542300453	chr7:150172433-150172434	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs555627609	chr7:150172572-150172573	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs143536804	chr7:150172671-150172672	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs187833515	chr7:150172677-150172678	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs28535865	chr7:150172682-150172683	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs533399159	chr7:150172722-150172723	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs199558249	chr7:150172728-150172729	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs534699362	chr7:150172735-150172736	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs74521423	chr7:150172796-150172797	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs151249845	chr7:150172814-150172815	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs140480554	chr7:150172817-150172818	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs549038590	chr7:150172841-150172842	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs565669706	chr7:150172849-150172850	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs528213829	chr7:150172872-150172873	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs551369499	chr7:150172931-150172932	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs571268332	chr7:150172934-150172935	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs372700659	chr7:150172938-150172939	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs150434802	chr7:150172941-150172942	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Heart disease	21282601	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Liver carcinoma	19366792	CNVD
Long-qt syndrome	17576883	CNVD
Bradycardia syndrome	17576883	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:971 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150158400-150174200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr7:150161200-150175200	Weak transcription	Small Intestine	intestine
3	chr7:150161200-150178400	Weak transcription	Esophagus	oesophagus
4	chr7:150162200-150176600	Weak transcription	Colonic Mucosa	Colon
5	chr7:150163600-150176600	Weak transcription	Primary B cells from cord blood	blood
6	chr7:150164200-150175400	Weak transcription	Gastric	stomach
7	chr7:150164400-150178000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr7:150165600-150175000	Genic enhancers	Primary T helper cells PMA-I stimulated	--
9	chr7:150165600-150176600	Weak transcription	Fetal Intestine Small	intestine
10	chr7:150165600-150179200	Weak transcription	Brain Hippocampus Middle	brain
11	chr7:150166400-150172600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr7:150166400-150176600	Weak transcription	Fetal Thymus	thymus
13	chr7:150166600-150172600	Weak transcription	Duodenum Mucosa	Duodenum
14	chr7:150166600-150172800	Weak transcription	Right Ventricle	heart
15	chr7:150166600-150173000	Weak transcription	Placenta	Placenta
16	chr7:150166600-150175200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr7:150166600-150175400	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
18	chr7:150166600-150178800	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr7:150166600-150179200	Weak transcription	Fetal Muscle Leg	muscle
20	chr7:150167400-150172800	Genic enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr7:150167800-150171800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr7:150167800-150173800	Weak transcription	Right Atrium	heart
23	chr7:150167800-150176200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr7:150168000-150175200	Strong transcription	HUVEC	blood vessel
25	chr7:150168000-150177400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr7:150168200-150174800	Strong transcription	Monocytes-CD14+_RO01746	blood
27	chr7:150168400-150174200	Strong transcription	Primary monocytes fromperipheralblood	blood
28	chr7:150168600-150176800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr7:150169000-150173600	Weak transcription	Primary hematopoietic stem cells	blood
30	chr7:150169600-150172200	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
31	chr7:150169600-150175200	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr7:150169600-150176800	Weak transcription	Liver	Liver
33	chr7:150169600-150177600	Weak transcription	Fetal Muscle Trunk	muscle
34	chr7:150169800-150173800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr7:150170400-150172400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
36	chr7:150170800-150172600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr7:150171000-150171800	Strong transcription	Primary T helper naive cells from peripheral blood	blood
38	chr7:150171000-150172400	Strong transcription	Primary T cells from cord blood	blood
39	chr7:150171200-150175200	Weak transcription	Adipose Nuclei	Adipose
40	chr7:150171400-150172400	Weak transcription	GM12878-XiMat	blood
41	chr7:150171400-150172600	Weak transcription	Left Ventricle	heart
42	chr7:150171400-150173600	Strong transcription	Primary T cells fromperipheralblood	blood
43	chr7:150171400-150173800	Weak transcription	Lung	lung
44	chr7:150171400-150175200	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr7:150171600-150172200	Strong transcription	Primary T helper cells fromperipheralblood	blood
46	chr7:150171600-150172200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr7:150171600-150172600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr7:150171600-150173800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr7:150171600-150173800	Weak transcription	Spleen	Spleen
50	chr7:150171800-150172400	Weak transcription	Primary T helper naive cells from peripheral blood	blood

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