Variant report

Variant	nsv523632
Chromosome Location	chr7:121754695-121802068
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:571)
CpG islands
(count:1159)
Chromatin interactive
region (count:13)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:571 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:121784246-121784741	HepG2	liver:	n/a	n/a
2	ATF1	chr7:121768589-121768594	K562	blood:	n/a	n/a
3	ATF2	chr7:121759596-121760262	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr7:121784316-121785029	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr7:121781923-121782552	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr7:121758615-121759301	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr7:121783455-121784234	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr7:121794769-121794802	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr7:121789070-121789555	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr7:121758296-121758564	GM12878	blood:	n/a	n/a
11	BHLHE40	chr7:121784303-121784745	GM12878	blood:	n/a	n/a
12	BHLHE40	chr7:121784076-121784880	HepG2	liver:	n/a	n/a
13	BRCA1	chr7:121758940-121759186	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr7:121759804-121759975	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr7:121784395-121784506	GM12878	blood:	n/a	n/a
16	BRCA1	chr7:121780652-121780798	H1-hESC	embryonic stem cell:	n/a	n/a
17	BRCA1	chr7:121783968-121784127	HepG2	liver:	n/a	n/a
18	BRCA1	chr7:121783534-121783659	GM12878	blood:	n/a	n/a
19	BRCA1	chr7:121784350-121784466	H1-hESC	embryonic stem cell:	n/a	n/a
20	CCNT2	chr7:121784518-121784548	K562	blood:	n/a	n/a
21	CEBPB	chr7:121766838-121767094	H1-hESC	embryonic stem cell:	n/a	chr7:121766964-121766975
22	CEBPB	chr7:121784079-121784630	A549	lung:	n/a	chr7:121784372-121784380
23	CEBPB	chr7:121766820-121767124	Hela-S3	cervix:	n/a	chr7:121766964-121766975
24	CEBPB	chr7:121784168-121784532	H1-hESC	embryonic stem cell:	n/a	chr7:121784372-121784380
25	CEBPB	chr7:121788852-121789288	H1-hESC	embryonic stem cell:	n/a	chr7:121789046-121789059
26	CEBPB	chr7:121784136-121784744	HepG2	liver:	n/a	chr7:121784372-121784380
27	CEBPB	chr7:121784148-121784794	A549	lung:	n/a	chr7:121784372-121784380
28	CEBPB	chr7:121770414-121770673	HepG2	liver:	n/a	n/a
29	CEBPB	chr7:121766837-121767140	HepG2	liver:	n/a	chr7:121766964-121766975
30	CEBPB	chr7:121770335-121770502	A549	lung:	n/a	n/a
31	CEBPB	chr7:121783663-121784532	IMR90	lung:	n/a	chr7:121784372-121784380
32	CEBPB	chr7:121784209-121784494	A549	lung:	n/a	chr7:121784372-121784380
33	CEBPB	chr7:121775451-121775693	H1-hESC	embryonic stem cell:	n/a	chr7:121775569-121775580 chr7:121775571-121775580
34	CEBPB	chr7:121775501-121775696	HepG2	liver:	n/a	chr7:121775569-121775580 chr7:121775571-121775580
35	CEBPB	chr7:121768220-121768571	HepG2	liver:	n/a	chr7:121768467-121768478
36	CEBPB	chr7:121784211-121784471	HepG2	liver:	n/a	chr7:121784372-121784380
37	CEBPB	chr7:121783961-121784745	HepG2	liver:	n/a	chr7:121784372-121784380
38	CEBPB	chr7:121784162-121784630	MCF-7	breast:	n/a	chr7:121784372-121784380
39	CEBPB	chr7:121784129-121784552	HepG2	liver:	n/a	chr7:121784372-121784380
40	CEBPB	chr7:121758782-121759370	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr7:121792113-121792301	A549	lung:	n/a	n/a
42	CEBPB	chr7:121784074-121784565	ECC-1	luminal epithelium:	n/a	chr7:121784372-121784380
43	CEBPB	chr7:121788185-121788286	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr7:121777560-121778807	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD1	chr7:121780072-121785040	H1-hESC	embryonic stem cell:	n/a	chr7:121783398-121783408 chr7:121783519-121783529
46	CHD1	chr7:121776148-121776349	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD1	chr7:121783368-121784984	IMR90	lung:	n/a	chr7:121783398-121783408 chr7:121783519-121783529
48	CHD1	chr7:121774120-121774209	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD1	chr7:121779100-121779666	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr7:121784120-121784651	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1159 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:121783544-121783594	RPTEC	kidney:	n/a
2	chr7:121783496-121783546	HNPCEpiC	eye:	n/a
3	chr7:121784564-121784614	ProgFib	skin:	n/a
4	chr7:121784249-121784299	LNCaP	prostate:	n/a
5	chr7:121787774-121787824	PFSK-1	brain:	n/a
6	chr7:121773889-121773939	AG10803	skin:	n/a
7	chr7:121783377-121783427	HCPEpiC	choroid plexus:	n/a
8	chr7:121784504-121784554	NT2-D1	testis:	n/a
9	chr7:121781778-121781828	HAEpiC	amniotic membrane:	n/a
10	chr7:121783496-121783546	T-47D	breast:	n/a
11	chr7:121783377-121783427	Hela-S3	cervix:	n/a
12	chr7:121784249-121784299	HepG2	liver:	n/a
13	chr7:121755577-121755627	MCF-7	breast:	n/a
14	chr7:121796366-121796416	HL-60	blood:	n/a
15	chr7:121784369-121784419	SAEC	small airway:	n/a
16	chr7:121784386-121784436	A549	lung:	n/a
17	chr7:121784356-121784406	Hepatocyte	liver:	n/a
18	chr7:121784102-121784152	HEEpiC	esophagus:	n/a
19	chr7:121784249-121784299	ovcar-3	ovarian:	n/a
20	chr7:121784596-121784646	BE2_C	brain:	n/a
21	chr7:121784386-121784436	NB4	blood:	n/a
22	chr7:121784249-121784299	HCM	heart:	n/a
23	chr7:121784369-121784419	HCM	heart:	n/a
24	chr7:121784369-121784419	GM12892	blood:	n/a
25	chr7:121784369-121784419	NT2-D1	testis:	n/a
26	chr7:121781778-121781828	HCT-116	colon:	n/a
27	chr7:121785331-121785381	HUVEC	blood vessel:	n/a
28	chr7:121784386-121784436	HIPEpiC	eye:	n/a
29	chr7:121785331-121785381	ovcar-3	ovarian:	n/a
30	chr7:121784351-121784401	T-47D	breast:	n/a
31	chr7:121781778-121781828	AoSMC	blood vessel:	n/a
32	chr7:121787774-121787824	HL-60	blood:	n/a
33	chr7:121784596-121784646	HepG2	liver:	n/a
34	chr7:121773889-121773939	GM06990	blood:	n/a
35	chr7:121767187-121767237	LNCaP	prostate:	n/a
36	chr7:121755577-121755627	SK-N-SH_RA	brain:	n/a
37	chr7:121783544-121783594	Caco-2	colon:	n/a
38	chr7:121784369-121784419	HL-60	blood:	n/a
39	chr7:121784369-121784419	HUVEC	blood vessel:	n/a
40	chr7:121784102-121784152	LNCaP	prostate:	n/a
41	chr7:121783496-121783546	GM06990	blood:	n/a
42	chr7:121784356-121784406	AG09319	gingival:	n/a
43	chr7:121784504-121784554	AG09309	skin:	n/a
44	chr7:121783496-121783546	Caco-2	colon:	n/a
45	chr7:121767187-121767237	Hela-S3	cervix:	n/a
46	chr7:121784504-121784554	SAEC	small airway:	n/a
47	chr7:121784351-121784401	LNCaP	prostate:	n/a
48	chr7:121784386-121784436	T-47D	breast:	n/a
49	chr7:121781778-121781828	HEK293	kidney:	embryo
50	chr7:121796366-121796416	AG04450	lung:	fetal

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:121755276..121758622-chr7:121759872..121762000,3	K562	blood:
2	chr7:121766737..121769191-chr7:121770279..121772578,2	K562	blood:
3	chr7:121766737..121769191-chr7:121770279..121772578,2	K562	blood:
4	chr7:121777883..121779429-chr7:121782207..121783905,2	K562	blood:
5	chr7:121768771..121771920-chr7:121774258..121777646,3	K562	blood:
6	chr7:121786887..121788984-chr7:121791394..121792980,2	MCF-7	breast:
7	chr7:121777883..121779429-chr7:121782207..121783905,2	K562	blood:
8	chr7:121768771..121771920-chr7:121774258..121777646,3	K562	blood:
9	chr7:121755276..121758622-chr7:121759872..121762000,3	K562	blood:
10	chr7:121779239..121781681-chr7:121799360..121802322,2	K562	blood:
11	chr7:121779239..121781681-chr7:121799360..121802322,2	K562	blood:
12	chr7:121777186..121779429-chr7:121782405..121785136,2	K562	blood:
13	chr7:121786887..121788984-chr7:121791394..121792980,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTPRZ1-7	chr7:121800542-121801007	NONHSAT123021
2	lnc-PTPRZ1-7	chr7:121801388-121802297	NONHSAT123021
3	lnc-PTPRZ1-7	chr7:121799354-121799831	NONHSAT123021

No data

Variant related genes	Relation type
ENSG00000226636	TF binding region
AASS	TF binding region
ENSG00000226636	CpG island
AASS	CpG island
ENSG00000008311	chromatin interactions

Extended variants
information (count: 1599 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1599 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4140745	chr7:121754695-121754696	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs576274196	chr7:121754720-121754721	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs188295361	chr7:121754733-121754734	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531732811	chr7:121754758-121754759	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs180812446	chr7:121754765-121754766	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs548261707	chr7:121754780-121754781	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs555852819	chr7:121754798-121754799	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs386717345	chr7:121754810-121754811	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572457150	chr7:121754880-121754881	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541555664	chr7:121754883-121754884	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs71571060	chr7:121754947-121754948	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs200164682	chr7:121754954-121754955	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs111846129	chr7:121754957-121754958	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs56052527	chr7:121754958-121754959	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543693025	chr7:121754959-121754960	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs529924347	chr7:121754982-121754983	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563654320	chr7:121755056-121755057	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs529344831	chr7:121755079-121755080	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs550970873	chr7:121755107-121755108	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146596013	chr7:121755136-121755137	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs141055314	chr7:121755140-121755141	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200905106	chr7:121755155-121755156	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs368840723	chr7:121755159-121755160	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs149832034	chr7:121755179-121755180	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs548570072	chr7:121755219-121755220	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201997703	chr7:121755225-121755226	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs145752623	chr7:121755226-121755227	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs148964986	chr7:121755263-121755264	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373480282	chr7:121755282-121755283	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs373940096	chr7:121755285-121755286	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369300181	chr7:121755305-121755306	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551484807	chr7:121755337-121755338	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs6947355	chr7:121755376-121755377	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs546446373	chr7:121755383-121755384	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs566770110	chr7:121755395-121755396	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs190994122	chr7:121755463-121755464	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376500510	chr7:121755519-121755520	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs71571061	chr7:121755530-121755531	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs71571062	chr7:121755569-121755570	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550868213	chr7:121755578-121755579	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182010595	chr7:121755583-121755584	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs538891165	chr7:121755587-121755588	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73426013	chr7:121755605-121755606	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs566111426	chr7:121755606-121755607	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534785353	chr7:121755626-121755627	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191746155	chr7:121755669-121755670	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs578085125	chr7:121755740-121755741	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372631953	chr7:121755751-121755752	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs543627971	chr7:121755754-121755755	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs183518577	chr7:121755760-121755761	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Glioblastoma multiforme	21922591	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute monocytic leukemia	16498392	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1305 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:121685000-121772000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr7:121703400-121755800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr7:121716000-121772000	Weak transcription	Osteobl	bone
4	chr7:121716000-121775600	Weak transcription	Colon Smooth Muscle	Colon
5	chr7:121716200-121758200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr7:121718000-121754800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr7:121718000-121756200	Weak transcription	Pancreas	Pancrea
8	chr7:121718200-121755000	Weak transcription	NHDF-Ad	bronchial
9	chr7:121722000-121755000	Weak transcription	HUVEC	blood vessel
10	chr7:121725800-121758400	Weak transcription	HSMMtube	muscle
11	chr7:121726000-121774400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
12	chr7:121726000-121776000	Weak transcription	Fetal Stomach	stomach
13	chr7:121731800-121770400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr7:121732000-121773600	Strong transcription	H1 Cell Line	embryonic stem cell
15	chr7:121739800-121760400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr7:121742600-121756200	Weak transcription	Right Ventricle	heart
17	chr7:121743000-121770200	Strong transcription	HUES48 Cell Line	embryonic stem cell
18	chr7:121743800-121776200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
19	chr7:121744600-121783200	Weak transcription	Lung	lung
20	chr7:121744800-121760400	Strong transcription	Liver	Liver
21	chr7:121744800-121775200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr7:121744800-121776800	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr7:121745600-121774000	Strong transcription	HUES6 Cell Line	embryonic stem cell
24	chr7:121747200-121757000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr7:121747200-121762400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr7:121747800-121755000	Weak transcription	Primary hematopoietic stem cells	blood
27	chr7:121747800-121756200	Weak transcription	Brain Angular Gyrus	brain
28	chr7:121747800-121756200	Weak transcription	Brain Cingulate Gyrus	brain
29	chr7:121747800-121760000	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr7:121747800-121760000	Weak transcription	Rectal Smooth Muscle	rectum
31	chr7:121747800-121775800	Strong transcription	HUES64 Cell Line	embryonic stem cell
32	chr7:121747800-121776200	Weak transcription	Fetal Brain Male	brain
33	chr7:121748000-121755400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr7:121748000-121755600	Weak transcription	Brain Anterior Caudate	brain
35	chr7:121748200-121763600	Weak transcription	HMEC	breast
36	chr7:121749600-121755000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr7:121749800-121756200	Weak transcription	Brain Germinal Matrix	brain
38	chr7:121750000-121756200	Weak transcription	Fetal Heart	heart
39	chr7:121750000-121776600	Weak transcription	Psoas Muscle	Psoas
40	chr7:121750200-121754800	Weak transcription	Fetal Intestine Small	intestine
41	chr7:121750200-121773600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr7:121750200-121775400	Weak transcription	Gastric	stomach
43	chr7:121750400-121775800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr7:121750600-121756200	Weak transcription	Spleen	Spleen
45	chr7:121750800-121769000	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr7:121750800-121775400	Weak transcription	Small Intestine	intestine
47	chr7:121751000-121757400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr7:121751000-121758800	Strong transcription	Skeletal Muscle Female	skeletal muscle
49	chr7:121751000-121759000	Strong transcription	Adipose Nuclei	Adipose
50	chr7:121751400-121758800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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