Variant report

Variant	nsv1034308
Chromosome Location	chr7:70190293-70230601
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:70217669-70218032	HepG2	liver:	n/a	n/a
2	ATF2	chr7:70226427-70227404	GM12878	blood:	n/a	n/a
3	ATF2	chr7:70193730-70194787	GM12878	blood:	n/a	n/a
4	ATF2	chr7:70226556-70227409	GM12878	blood:	n/a	n/a
5	ATF2	chr7:70191802-70192414	GM12878	blood:	n/a	n/a
6	ATF2	chr7:70194222-70194708	GM12878	blood:	n/a	n/a
7	ATF2	chr7:70191740-70192428	GM12878	blood:	n/a	n/a
8	ATF2	chr7:70228852-70229895	GM12878	blood:	n/a	n/a
9	ATF2	chr7:70228752-70229755	GM12878	blood:	n/a	n/a
10	BATF	chr7:70192129-70192402	GM12878	blood:	n/a	n/a
11	BATF	chr7:70195779-70196118	GM12878	blood:	n/a	chr7:70195970-70195981
12	BATF	chr7:70195849-70196064	GM12878	blood:	n/a	chr7:70195970-70195981
13	BATF	chr7:70226797-70227424	GM12878	blood:	n/a	chr7:70227126-70227136 chr7:70227125-70227136
14	BATF	chr7:70226780-70227411	GM12878	blood:	n/a	chr7:70227126-70227136 chr7:70227125-70227136
15	BATF	chr7:70229142-70229667	GM12878	blood:	n/a	n/a
16	BATF	chr7:70229244-70229678	GM12878	blood:	n/a	n/a
17	BATF	chr7:70191842-70192464	GM12878	blood:	n/a	n/a
18	BCL11A	chr7:70229020-70229654	GM12878	blood:	n/a	chr7:70229064-70229072
19	BCL11A	chr7:70192090-70192386	GM12878	blood:	n/a	n/a
20	BCL11A	chr7:70226689-70227260	GM12878	blood:	n/a	chr7:70226852-70226861 chr7:70226921-70226930
21	BCL11A	chr7:70194287-70194666	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:70191921-70192224	GM12878	blood:	n/a	chr7:70191981-70191990
23	BCL11A	chr7:70193763-70194026	H1-hESC	embryonic stem cell:	n/a	n/a
24	BCL11A	chr7:70229154-70229733	GM12878	blood:	n/a	n/a
25	BCL11A	chr7:70226751-70227076	GM12878	blood:	n/a	chr7:70226852-70226861 chr7:70226921-70226930
26	BCL3	chr7:70228999-70229661	GM12878	blood:	n/a	chr7:70229064-70229072
27	BCL3	chr7:70191976-70192347	GM12878	blood:	n/a	chr7:70191981-70191990
28	BCL3	chr7:70226630-70227241	GM12878	blood:	n/a	chr7:70226852-70226861 chr7:70226921-70226930
29	BCL3	chr7:70191822-70192406	GM12878	blood:	n/a	chr7:70191981-70191990
30	BCL3	chr7:70228934-70229775	GM12878	blood:	n/a	chr7:70229064-70229072
31	BCL3	chr7:70194233-70194787	GM12878	blood:	n/a	n/a
32	BCLAF1	chr7:70228851-70229760	GM12878	blood:	n/a	chr7:70228879-70228888 chr7:70229064-70229072
33	BCLAF1	chr7:70191843-70192358	GM12878	blood:	n/a	chr7:70191981-70191990
34	BCLAF1	chr7:70226582-70227292	GM12878	blood:	n/a	chr7:70226852-70226861 chr7:70226921-70226930
35	BCLAF1	chr7:70228896-70229709	GM12878	blood:	n/a	chr7:70229064-70229072
36	BCLAF1	chr7:70194201-70194815	GM12878	blood:	n/a	n/a
37	BCLAF1	chr7:70191621-70192431	GM12878	blood:	n/a	chr7:70191981-70191990
38	BHLHE40	chr7:70217731-70217842	HepG2	liver:	n/a	n/a
39	BHLHE40	chr7:70191415-70192356	GM12878	blood:	n/a	n/a
40	BHLHE40	chr7:70228638-70230174	GM12878	blood:	n/a	n/a
41	BHLHE40	chr7:70226684-70227274	GM12878	blood:	n/a	n/a
42	BHLHE40	chr7:70201669-70201693	GM12878	blood:	n/a	n/a
43	BHLHE40	chr7:70209600-70209763	GM12878	blood:	n/a	n/a
44	BHLHE40	chr7:70193857-70194815	GM12878	blood:	n/a	n/a
45	BHLHE40	chr7:70226125-70226429	GM12878	blood:	n/a	n/a
46	CEBPB	chr7:70201625-70202591	IMR90	lung:	n/a	chr7:70201840-70201851 chr7:70201841-70201850 chr7:70201841-70201850 chr7:70201839-70201850 chr7:70201841-70201850 chr7:70201839-70201852 chr7:70201841-70201850
47	CEBPB	chr7:70226572-70227419	GM12878	blood:	n/a	n/a
48	CEBPB	chr7:70201772-70201910	HepG2	liver:	n/a	chr7:70201840-70201851 chr7:70201841-70201850 chr7:70201841-70201850 chr7:70201839-70201850 chr7:70201841-70201850 chr7:70201839-70201852 chr7:70201841-70201850
49	CEBPB	chr7:70201715-70202034	H1-hESC	embryonic stem cell:	n/a	chr7:70201840-70201851 chr7:70201841-70201850 chr7:70201841-70201850 chr7:70201839-70201850 chr7:70201841-70201850 chr7:70201839-70201852 chr7:70201841-70201850
50	CEBPB	chr7:70229106-70229751	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:70194602-70194652	SAEC	small airway:	n/a
2	chr7:70194602-70194652	SAEC	small airway:	n/a
3	chr7:70216208-70216258	U87	brain:	n/a
4	chr7:70203221-70203271	H1-hESC	embryonic stem cell:	embryo
5	chr7:70198123-70198173	HCM	heart:	n/a
6	chr7:70209588-70209638	PANC-1	pancreas:	n/a
7	chr7:70216208-70216258	NB4	blood:	n/a
8	chr7:70203221-70203271	GM12891	blood:	n/a
9	chr7:70198123-70198173	NH-A	brain:	n/a
10	chr7:70209588-70209638	HRPEpiC	eye:	n/a
11	chr7:70198123-70198173	MCF-7	breast:	n/a
12	chr7:70216208-70216258	HCM	heart:	n/a
13	chr7:70203221-70203271	Hela-S3	cervix:	n/a
14	chr7:70194602-70194652	NB4	blood:	n/a
15	chr7:70198123-70198173	HepG2	liver:	n/a
16	chr7:70198123-70198173	HIPEpiC	eye:	n/a
17	chr7:70203221-70203271	HNPCEpiC	eye:	n/a
18	chr7:70194602-70194652	PrEC	prostate:	n/a
19	chr7:70200532-70200582	NHBE	bronchial:	n/a
20	chr7:70200532-70200582	HPAEpiC	pulmonary alveolar:	n/a
21	chr7:70200532-70200582	HCF	heart:	n/a
22	chr7:70200532-70200582	SKMC	muscle:	n/a
23	chr7:70203221-70203271	GM06990	blood:	n/a
24	chr7:70198123-70198173	H1-hESC	embryonic stem cell:	embryo
25	chr7:70200532-70200582	SAEC	small airway:	n/a
26	chr7:70216208-70216258	GM12892	blood:	n/a
27	chr7:70200532-70200582	Hela-S3	cervix:	n/a
28	chr7:70209588-70209638	NT2-D1	testis:	n/a
29	chr7:70203221-70203271	NB4	blood:	n/a
30	chr7:70209588-70209638	HCPEpiC	choroid plexus:	n/a
31	chr7:70203221-70203271	HUVEC	blood vessel:	n/a
32	chr7:70216208-70216258	NHDF-neo	bronchial:	n/a
33	chr7:70216208-70216258	GM12878	blood:	n/a
34	chr7:70203221-70203271	AG09309	skin:	n/a
35	chr7:70198123-70198173	SKMC	muscle:	n/a
36	chr7:70209588-70209638	GM12878	blood:	n/a
37	chr7:70203221-70203271	AG04449	skin:	fetal
38	chr7:70209588-70209638	AoSMC	blood vessel:	n/a
39	chr7:70216208-70216258	PFSK-1	brain:	n/a
40	chr7:70203221-70203271	HCM	heart:	n/a
41	chr7:70216208-70216258	HPAEpiC	pulmonary alveolar:	n/a
42	chr7:70216208-70216258	HRPEpiC	eye:	n/a
43	chr7:70198123-70198173	Caco-2	colon:	n/a
44	chr7:70209588-70209638	NHDF-neo	bronchial:	n/a
45	chr7:70216208-70216258	ProgFib	skin:	n/a
46	chr7:70216208-70216258	SK-N-MC	brain:	n/a
47	chr7:70200532-70200582	HCT-116	colon:	n/a
48	chr7:70203221-70203271	HPAEpiC	pulmonary alveolar:	n/a
49	chr7:70198123-70198173	HMEC	breast:	n/a
50	chr7:70194602-70194652	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:70182197..70184832-chr7:70191535..70193515,2	MCF-7	breast:
2	chr7:70184183..70185798-chr7:70197589..70200298,2	MCF-7	breast:
3	chr7:70157661..70160081-chr7:70223262..70226171,2	MCF-7	breast:
4	chr6:39278169..39279933-chr7:70204739..70207119,2	MCF-7	breast:
5	chr7:70212124..70215899-chr7:70217656..70219621,3	K562	blood:
6	chr7:70212124..70215899-chr7:70217656..70219621,3	K562	blood:
7	chr7:70222449..70225424-chr7:70225544..70227809,2	MCF-7	breast:
8	chr7:70222449..70225424-chr7:70225544..70227809,2	MCF-7	breast:
9	chr7:70225764..70228069-chr7:70229252..70232083,2	K562	blood:

Variant related genes	Relation type
AUTS2	TF binding region
AUTS2	CpG island
ENSG00000158321	chromatin interactions

Extended variants
information (count: 1750 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1750 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187778541	chr7:70190301-70190302	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs142897041	chr7:70190323-70190324	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs567281573	chr7:70190354-70190355	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs7801472	chr7:70190384-70190385	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
5	rs556410638	chr7:70190400-70190401	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs192652678	chr7:70190404-70190405	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs75254148	chr7:70190408-70190409	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs538801619	chr7:70190448-70190449	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs370011089	chr7:70190455-70190456	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs76909467	chr7:70190503-70190504	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs184298746	chr7:70190552-70190553	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs572198206	chr7:70190560-70190561	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs556955155	chr7:70190578-70190579	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs367738574	chr7:70190605-70190606	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs187238086	chr7:70190632-70190633	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs562373443	chr7:70190665-70190666	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs541115178	chr7:70190707-70190708	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs75360622	chr7:70190712-70190713	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs560244387	chr7:70190718-70190719	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs191683323	chr7:70190817-70190818	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs73165392	chr7:70190873-70190874	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs567441691	chr7:70190878-70190879	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs7805679	chr7:70190880-70190881	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs549747256	chr7:70190963-70190964	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs149763494	chr7:70190966-70190967	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs147646442	chr7:70190995-70190996	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs374934368	chr7:70191125-70191126	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs10247394	chr7:70191186-70191187	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs566223844	chr7:70191195-70191196	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs563613468	chr7:70191227-70191228	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs73165396	chr7:70191244-70191245	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs533365119	chr7:70191329-70191330	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs371600890	chr7:70191341-70191342	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs370547506	chr7:70191420-70191421	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs184550785	chr7:70191447-70191448	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs7805642	chr7:70191538-70191539	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs577566458	chr7:70191561-70191562	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs76500555	chr7:70191562-70191563	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs560202259	chr7:70191619-70191620	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs190075824	chr7:70191624-70191625	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs542389882	chr7:70191674-70191675	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs559500465	chr7:70191741-70191742	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs560781188	chr7:70191744-70191745	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs17684191	chr7:70191801-70191802	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs550054666	chr7:70191840-70191841	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs571571628	chr7:70191851-70191852	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs76947681	chr7:70191920-70191921	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs548037980	chr7:70191932-70191933	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs146116582	chr7:70191949-70191950	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs568364541	chr7:70191992-70191993	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17170743	CNVD
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
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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16461572	CNVD
Acute monocytic leukemia	16498392	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neurodevelopmental disorder	22521361	CNVD
Renal cell carcinoma	18765545	CNVD
Chordoma	18071362	CNVD
Williams Syndrome	20824207	CNVD
Dyslexia	22102821	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1485 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:70161800-70191200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr7:70162200-70201600	Weak transcription	Primary B cells from cord blood	blood
3	chr7:70176200-70201600	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr7:70176400-70192000	Weak transcription	HMEC	breast
5	chr7:70176400-70193800	Weak transcription	NH-A	brain
6	chr7:70179800-70192000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr7:70179800-70201600	Weak transcription	Rectal Smooth Muscle	rectum
8	chr7:70180000-70192200	Weak transcription	Aorta	Aorta
9	chr7:70180200-70190400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr7:70180200-70193800	Weak transcription	Fetal Intestine Small	intestine
11	chr7:70182600-70190400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr7:70182600-70194000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr7:70183000-70194000	Weak transcription	Fetal Stomach	stomach
14	chr7:70183000-70201600	Weak transcription	Fetal Muscle Leg	muscle
15	chr7:70183200-70191800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr7:70183200-70193800	Weak transcription	Thymus	Thymus
17	chr7:70183200-70194000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr7:70183200-70200200	Weak transcription	Ovary	ovary
19	chr7:70183200-70201800	Weak transcription	Pancreas	Pancrea
20	chr7:70183400-70193800	Weak transcription	Fetal Muscle Trunk	muscle
21	chr7:70183400-70194000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr7:70183400-70195400	Weak transcription	HSMM	muscle
23	chr7:70183600-70197600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr7:70184400-70195200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr7:70184600-70193000	Enhancers	Liver	Liver
26	chr7:70185800-70191600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr7:70185800-70191600	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr7:70185800-70192000	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr7:70185800-70197600	Weak transcription	HSMMtube	muscle
30	chr7:70186000-70191400	Weak transcription	Fetal Heart	heart
31	chr7:70186000-70191600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr7:70186000-70195400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr7:70186400-70190400	Weak transcription	Fetal Brain Male	brain
34	chr7:70186400-70198200	Weak transcription	Dnd41	blood
35	chr7:70187000-70201200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr7:70187200-70191600	Weak transcription	Fetal Brain Female	brain
37	chr7:70187800-70191400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr7:70188400-70191400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr7:70188600-70192600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr7:70188600-70193000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr7:70188800-70191200	Weak transcription	Primary T cells from cord blood	blood
42	chr7:70189200-70193000	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr7:70189200-70193800	Weak transcription	Lung	lung
44	chr7:70189600-70190800	Enhancers	Skeletal Muscle Female	skeletal muscle
45	chr7:70189600-70191000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr7:70189800-70190400	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr7:70189800-70190800	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr7:70189800-70191000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr7:70189800-70191400	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr7:70189800-70191400	Enhancers	HUES64 Cell Line	embryonic stem cell

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