Variant report

Variant	esv1792357
Chromosome Location	chr7:124470044-124506088
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	chr7:124479750-124480129	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:124496343-124496696	HepG2	liver:	n/a	chr7:124496382-124496398
3	ARID3A	chr7:124480552-124480789	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:124496286-124496702	K562	blood:	n/a	chr7:124496382-124496398
5	ARID3A	chr7:124475378-124475473	K562	blood:	n/a	n/a
6	BACH1	chr7:124484942-124484968	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr7:124490304-124490368	K562	blood:	n/a	n/a
8	CEBPB	chr7:124480599-124480774	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr7:124496381-124496691	K562	blood:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
10	CTCF	chr7:124496640-124496790	A549	lung:	n/a	n/a
11	CTCF	chr7:124496351-124496659	SK-N-SH_RA	brain:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
12	CTCF	chr7:124496420-124496570	GM12871	blood:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
13	CTCF	chr7:124480592-124480794	HUVEC	blood vessel:	n/a	chr7:124480667-124480688
14	CTCF	chr7:124496440-124496590	HAc	cerebellar:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
15	CTCF	chr7:124496460-124496610	HMEC	breast:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
16	CTCF	chr7:124496500-124496650	RPTEC	kidney:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
17	CTCF	chr7:124496560-124496710	MCF-7	breast:	n/a	n/a
18	CTCF	chr7:124496440-124496590	GM12874	blood:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
19	CTCF	chr7:124496520-124496670	GM12864	blood:	n/a	chr7:124496528-124496536 chr7:124496523-124496541
20	CTCF	chr7:124496421-124496710	H1-hESC	embryonic stem cell:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
21	CTCF	chr7:124496420-124496570	K562	blood:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
22	CTCF	chr7:124496520-124496670	HUVEC	blood vessel:	n/a	chr7:124496528-124496536 chr7:124496523-124496541
23	CTCF	chr7:124480604-124480772	LNCaP	prostate:	n/a	chr7:124480667-124480688
24	CTCF	chr7:124496440-124496590	SK-N-SH_RA	brain:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
25	CTCF	chr7:124496139-124496901	SK-N-SH	brain:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
26	CTCF	chr7:124497680-124497830	GM12871	blood:	n/a	n/a
27	CTCF	chr7:124496440-124496590	HFF-Myc	foreskin:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
28	CTCF	chr7:124496136-124496958	A549	lung:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
29	CTCF	chr7:124496500-124496650	GM12870	blood:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
30	CTCF	chr7:124496420-124496570	NHEK	skin:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
31	CTCF	chr7:124496700-124496850	MCF-7	breast:	n/a	n/a
32	CTCF	chr7:124496417-124496635	Hela-S3	cervix:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
33	CTCF	chr7:124496480-124496630	NHLF	lung:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
34	CTCF	chr7:124496500-124496650	GM12875	blood:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
35	CTCF	chr7:124496440-124496590	HRE	kidney:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
36	CTCF	chr7:124496420-124496570	GM12874	blood:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
37	CTCF	chr7:124480421-124480923	SK-N-SH	brain:	n/a	chr7:124480667-124480688
38	CTCF	chr7:124496460-124496610	HA-sp	spinal cord:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
39	CTCF	chr7:124496460-124496610	AG04450	lung:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
40	CTCF	chr7:124480740-124480890	BE2_C	brain:	n/a	n/a
41	CTCF	chr7:124496460-124496610	HepG2	liver:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
42	CTCF	chr7:124496466-124496663	MCF-7	breast:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
43	CTCF	chr7:124496500-124496650	SAEC	small airway:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
44	CTCF	chr7:124496460-124496610	AG09309	skin:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
45	CTCF	chr7:124496480-124496630	Hela-S3	cervix:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
46	CTCF	chr7:124496440-124496590	NHDF-neo	bronchial:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
47	CTCF	chr7:124496440-124496590	HRPEpiC	eye:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
48	CTCF	chr7:124496460-124496610	HEK293	kidney:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
49	CTCF	chr7:124496460-124496610	HEEpiC	esophagus:	n/a	chr7:124496518-124496539 chr7:124496528-124496536 chr7:124496523-124496541
50	CTCF	chr7:124480580-124480730	HCPEpiC	choroid plexus:	n/a	chr7:124480667-124480688

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:124498272-124498322	Caco-2	colon:	n/a
2	chr7:124498272-124498322	SK-N-SH_RA	brain:	n/a
3	chr7:124498272-124498322	H1-hESC	embryonic stem cell:	embryo
4	chr7:124498272-124498322	HIPEpiC	eye:	n/a
5	chr7:124498272-124498322	MCF-7	breast:	n/a
6	chr7:124498272-124498322	ovcar-3	ovarian:	n/a
7	chr7:124498272-124498322	GM12878	blood:	n/a
8	chr7:124498272-124498322	HepG2	liver:	n/a
9	chr7:124498272-124498322	NT2-D1	testis:	n/a
10	chr7:124498272-124498322	IMR90	lung:	fetal
11	chr7:124498272-124498322	GM19239	blood:	n/a
12	chr7:124498272-124498322	AG04449	skin:	fetal
13	chr7:124498272-124498322	HPAEpiC	pulmonary alveolar:	n/a
14	chr7:124498272-124498322	HEK293	kidney:	embryo
15	chr7:124498272-124498322	HCPEpiC	choroid plexus:	n/a
16	chr7:124498272-124498322	NHDF-neo	bronchial:	n/a
17	chr7:124498272-124498322	LNCaP	prostate:	n/a
18	chr7:124498272-124498322	HCM	heart:	n/a
19	chr7:124498272-124498322	PrEC	prostate:	n/a
20	chr7:124498272-124498322	HRCEpiC	kidney:	n/a
21	chr7:124498272-124498322	ProgFib	skin:	n/a
22	chr7:124498272-124498322	SAEC	small airway:	n/a
23	chr7:124498272-124498322	CMK	blood:	n/a
24	chr7:124498272-124498322	HCT-116	colon:	n/a
25	chr7:124498272-124498322	NHBE	bronchial:	n/a
26	chr7:124498272-124498322	BJ	skin:	n/a
27	chr7:124498272-124498322	HL-60	blood:	n/a
28	chr7:124498272-124498322	AG10803	skin:	n/a
29	chr7:124498272-124498322	HRE	kidney:	n/a
30	chr7:124498272-124498322	HAEpiC	amniotic membrane:	n/a
31	chr7:124498272-124498322	GM12892	blood:	n/a
32	chr7:124498272-124498322	K562	blood:	n/a
33	chr7:124498272-124498322	AoSMC	blood vessel:	n/a
34	chr7:124498272-124498322	SKMC	muscle:	n/a
35	chr7:124498272-124498322	SK-N-SH	brain:	n/a
36	chr7:124498272-124498322	GM06990	blood:	n/a
37	chr7:124498272-124498322	NB4	blood:	n/a
38	chr7:124498272-124498322	ECC-1	luminal epithelium:	n/a
39	chr7:124498272-124498322	GM12891	blood:	n/a
40	chr7:124498272-124498322	PFSK-1	brain:	n/a
41	chr7:124498272-124498322	A549	lung:	n/a
42	chr7:124498272-124498322	MCF10A-Er-Src	breast:	n/a
43	chr7:124498272-124498322	T-47D	breast:	n/a
44	chr7:124498272-124498322	AG09309	skin:	n/a
45	chr7:124498272-124498322	HCF	heart:	n/a
46	chr7:124498272-124498322	AG04450	lung:	fetal
47	chr7:124498272-124498322	U87	brain:	n/a
48	chr7:124498272-124498322	NH-A	brain:	n/a
49	chr7:124498272-124498322	Hepatocyte	liver:	n/a
50	chr7:124498272-124498322	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:124481779..124483829-chr7:124493463..124496248,2	K562	blood:
2	chr7:124481779..124483829-chr7:124493463..124496248,2	K562	blood:
3	chr7:124490021..124491780-chr7:124492747..124495202,2	K562	blood:
4	chr7:124495485..124496005-chr7:124636684..124637532,2	MCF-7	breast:
5	chr7:123811047..123811686-chr7:124496461..124497015,2	MCF-7	breast:
6	chr7:124504726..124507196-chr7:124509584..124511156,2	K562	blood:
7	chr7:123795289..123796073-chr7:124496029..124496841,2	MCF-7	breast:
8	chr7:123795257..123796091-chr7:124480511..124481123,2	MCF-7	breast:
9	chr7:124477918..124479751-chr7:124480118..124483103,2	MCF-7	breast:
10	chr7:123793036..123793586-chr7:124480618..124481248,2	MCF-7	breast:
11	chr7:124477564..124479634-chr7:124483679..124485417,2	K562	blood:
12	chr7:123792601..123793517-chr7:124480532..124481197,4	MCF-7	breast:
13	chr7:124482329..124484831-chr7:124493791..124496248,2	K562	blood:
14	chr7:123607226..123607809-chr7:124496082..124496837,2	MCF-7	breast:
15	chr7:124484767..124486833-chr7:124496762..124499630,2	K562	blood:
16	chr7:123383491..123385633-chr7:124494665..124496750,2	K562	blood:
17	chr7:124477564..124479634-chr7:124483679..124485417,2	K562	blood:
18	chr7:124485031..124486587-chr7:124492605..124494106,2	MCF-7	breast:

Variant related genes	Relation type
POT1	TF binding region
POT1	CpG island
ENSG00000128513	chromatin interactions

Extended variants
information (count: 1319 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1319 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549294608	chr7:124470065-124470066	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs553238738	chr7:124470094-124470095	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs17147583	chr7:124470125-124470126	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs73223541	chr7:124470139-124470140	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs561579069	chr7:124470148-124470149	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs558259322	chr7:124470278-124470279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs575203893	chr7:124470290-124470291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs57891354	chr7:124470391-124470392	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs557656361	chr7:124470394-124470395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531984884	chr7:124470512-124470513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs185304542	chr7:124470544-124470545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs189420268	chr7:124470589-124470590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs538093643	chr7:124470656-124470657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559545703	chr7:124470658-124470659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs540793389	chr7:124470660-124470661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs550204435	chr7:124470708-124470709	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs559144543	chr7:124470732-124470733	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs371780760	chr7:124470734-124470735	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs75799727	chr7:124470867-124470868	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
20	rs4728009	chr7:124470961-124470962	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs143001766	chr7:124470999-124471000	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs181460019	chr7:124471036-124471037	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs375865792	chr7:124471048-124471049	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs184878747	chr7:124471080-124471081	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs564935384	chr7:124471239-124471240	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs538764862	chr7:124471272-124471273	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs534256240	chr7:124471352-124471353	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs546815200	chr7:124471354-124471355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs566713940	chr7:124471416-124471417	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs538316801	chr7:124471429-124471430	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370466260	chr7:124471432-124471433	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568729891	chr7:124471486-124471487	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs372453472	chr7:124471582-124471583	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200370932	chr7:124471587-124471588	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs537862268	chr7:124471588-124471589	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs148199364	chr7:124471589-124471590	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs573969679	chr7:124471595-124471596	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536592095	chr7:124471604-124471605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs79931811	chr7:124471657-124471658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs150385087	chr7:124471663-124471664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369614747	chr7:124471691-124471692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs4141073	chr7:124471754-124471755	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs577559057	chr7:124471840-124471841	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs565397384	chr7:124471843-124471844	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs114988988	chr7:124471853-124471854	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs189381508	chr7:124471854-124471855	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs561313600	chr7:124471884-124471885	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs4731217	chr7:124471889-124471890	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs556703624	chr7:124471900-124471901	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs531996506	chr7:124471959-124471960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	21635232	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myxofibrosarcoma	20639860	CNVD

Chromatin state (count:541 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:124452800-124475000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr7:124454400-124497600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr7:124454600-124501400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr7:124457600-124497600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr7:124459000-124497800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr7:124459200-124497600	Weak transcription	Pancreas	Pancrea
7	chr7:124459200-124499400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr7:124459400-124497600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr7:124459400-124497600	Weak transcription	Brain Anterior Caudate	brain
10	chr7:124460200-124483400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr7:124460400-124488600	Weak transcription	HSMMtube	muscle
12	chr7:124460600-124486200	Weak transcription	Brain Substantia Nigra	brain
13	chr7:124460800-124476200	Weak transcription	Fetal Brain Male	brain
14	chr7:124461000-124499200	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr7:124461000-124499600	Weak transcription	Stomach Smooth Muscle	stomach
16	chr7:124461400-124530800	Weak transcription	NHDF-Ad	bronchial
17	chr7:124461600-124490600	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr7:124461600-124493400	Weak transcription	Primary neutrophils fromperipheralblood	blood
19	chr7:124461600-124499800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr7:124462200-124474600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr7:124462200-124495000	Weak transcription	Brain Cingulate Gyrus	brain
22	chr7:124462200-124498200	Weak transcription	Psoas Muscle	Psoas
23	chr7:124462200-124510200	Weak transcription	Brain Angular Gyrus	brain
24	chr7:124462200-124568200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr7:124462400-124475000	Weak transcription	Thymus	Thymus
26	chr7:124462400-124488200	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr7:124462400-124497400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr7:124462600-124479800	Weak transcription	HepG2	liver
29	chr7:124462600-124504000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr7:124464000-124470600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr7:124464000-124506400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr7:124464000-124510400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
33	chr7:124464200-124475000	Weak transcription	Left Ventricle	heart
34	chr7:124464200-124480200	Weak transcription	HUVEC	blood vessel
35	chr7:124464200-124487000	Weak transcription	Primary hematopoietic stem cells	blood
36	chr7:124464200-124519400	Weak transcription	Brain Hippocampus Middle	brain
37	chr7:124464400-124475000	Weak transcription	Fetal Kidney	kidney
38	chr7:124464400-124497200	Weak transcription	Brain Germinal Matrix	brain
39	chr7:124464400-124497600	Weak transcription	Lung	lung
40	chr7:124464400-124508800	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr7:124464600-124486000	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr7:124464600-124487800	Weak transcription	Primary B cells from cord blood	blood
43	chr7:124464600-124530600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr7:124465000-124489400	Weak transcription	Hela-S3	cervix
45	chr7:124465400-124473200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr7:124465400-124479000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr7:124466000-124491000	Weak transcription	Fetal Intestine Small	intestine
48	chr7:124466200-124486200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr7:124466400-124474800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr7:124466400-124479400	Weak transcription	HUES48 Cell Line	embryonic stem cell

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