Variant report

Variant	nsv1026722
Chromosome Location	chr4:129801602-129929219
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:470)
CpG islands
(count:62)
Chromatin interactive
region (count:39)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:470 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:129866424-129866624	K562	blood:	n/a	n/a
2	ARID3A	chr4:129879403-129879765	HepG2	liver:	n/a	n/a
3	ATF2	chr4:129838788-129839413	GM12878	blood:	n/a	n/a
4	ATF2	chr4:129838782-129839408	GM12878	blood:	n/a	n/a
5	ATF2	chr4:129834221-129834957	GM12878	blood:	n/a	n/a
6	ATF2	chr4:129834181-129834816	GM12878	blood:	n/a	n/a
7	ATF2	chr4:129837715-129838462	GM12878	blood:	n/a	n/a
8	ATF2	chr4:129837905-129838481	GM12878	blood:	n/a	n/a
9	BACH1	chr4:129902627-129902712	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:129901252-129901452	K562	blood:	n/a	n/a
11	BATF	chr4:129837910-129838268	GM12878	blood:	n/a	n/a
12	BATF	chr4:129827779-129828010	GM12878	blood:	n/a	chr4:129827877-129827888
13	BATF	chr4:129838911-129839317	GM12878	blood:	n/a	n/a
14	BATF	chr4:129838922-129839343	GM12878	blood:	n/a	n/a
15	BCL11A	chr4:129839033-129839295	GM12878	blood:	n/a	n/a
16	BCL11A	chr4:129838977-129839324	GM12878	blood:	n/a	n/a
17	BCL3	chr4:129834252-129834735	GM12878	blood:	n/a	n/a
18	BCL3	chr4:129834324-129834632	GM12878	blood:	n/a	n/a
19	BCL3	chr4:129838908-129839307	GM12878	blood:	n/a	n/a
20	BCLAF1	chr4:129838854-129839425	GM12878	blood:	n/a	n/a
21	BCLAF1	chr4:129837719-129838296	GM12878	blood:	n/a	n/a
22	BCLAF1	chr4:129837821-129838334	GM12878	blood:	n/a	n/a
23	BCLAF1	chr4:129838883-129839358	GM12878	blood:	n/a	n/a
24	BHLHE40	chr4:129838803-129839362	GM12878	blood:	n/a	n/a
25	BHLHE40	chr4:129838002-129838412	GM12878	blood:	n/a	n/a
26	BRCA1	chr4:129846236-129846257	GM12878	blood:	n/a	n/a
27	CBX3	chr4:129901088-129901449	HCT-116	colon:	n/a	n/a
28	CCNT2	chr4:129861639-129861803	K562	blood:	n/a	n/a
29	CEBPB	chr4:129801803-129802175	A549	lung:	n/a	chr4:129801978-129801989
30	CEBPB	chr4:129801797-129802171	IMR90	lung:	n/a	chr4:129801978-129801989
31	CEBPB	chr4:129862212-129862459	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr4:129862172-129862511	K562	blood:	n/a	n/a
33	CEBPB	chr4:129905387-129905697	HepG2	liver:	n/a	chr4:129905546-129905557
34	CEBPB	chr4:129801795-129802175	K562	blood:	n/a	chr4:129801978-129801989
35	CEBPB	chr4:129879417-129879725	MCF-7	breast:	n/a	chr4:129879570-129879581 chr4:129879569-129879582
36	CEBPB	chr4:129801800-129802160	H1-hESC	embryonic stem cell:	n/a	chr4:129801978-129801989
37	CEBPB	chr4:129862245-129862448	K562	blood:	n/a	n/a
38	CEBPB	chr4:129801778-129802181	ECC-1	luminal epithelium:	n/a	chr4:129801978-129801989
39	CEBPB	chr4:129801770-129802182	A549	lung:	n/a	chr4:129801978-129801989
40	CEBPB	chr4:129900239-129900408	IMR90	lung:	n/a	n/a
41	CEBPB	chr4:129924790-129925052	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr4:129862131-129862536	K562	blood:	n/a	n/a
43	CEBPB	chr4:129905491-129905623	K562	blood:	n/a	chr4:129905546-129905557
44	CEBPB	chr4:129879382-129879762	HepG2	liver:	n/a	chr4:129879570-129879581 chr4:129879569-129879582
45	CEBPB	chr4:129905450-129905683	IMR90	lung:	n/a	chr4:129905546-129905557
46	CEBPB	chr4:129801817-129802128	ECC-1	luminal epithelium:	n/a	chr4:129801978-129801989
47	CEBPB	chr4:129801840-129802139	Hela-S3	cervix:	n/a	chr4:129801978-129801989
48	CEBPB	chr4:129801795-129802172	HepG2	liver:	n/a	chr4:129801978-129801989
49	CEBPB	chr4:129918421-129918579	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr4:129879348-129879753	HepG2	liver:	n/a	chr4:129879570-129879581 chr4:129879569-129879582

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:129805520-129805570	NH-A	brain:	n/a
2	chr4:129805520-129805570	NH-A	brain:	n/a
3	chr4:129805520-129805570	HCM	heart:	n/a
4	chr4:129805520-129805570	AG04450	lung:	fetal
5	chr4:129805520-129805570	CMK	blood:	n/a
6	chr4:129805520-129805570	A549	lung:	n/a
7	chr4:129805520-129805570	AG09319	gingival:	n/a
8	chr4:129805520-129805570	HRPEpiC	eye:	n/a
9	chr4:129805520-129805570	K562	blood:	n/a
10	chr4:129805520-129805570	LNCaP	prostate:	n/a
11	chr4:129805520-129805570	HCPEpiC	choroid plexus:	n/a
12	chr4:129805520-129805570	NT2-D1	testis:	n/a
13	chr4:129805520-129805570	HIPEpiC	eye:	n/a
14	chr4:129805520-129805570	ProgFib	skin:	n/a
15	chr4:129805520-129805570	PANC-1	pancreas:	n/a
16	chr4:129805520-129805570	HPAEpiC	pulmonary alveolar:	n/a
17	chr4:129805520-129805570	SK-N-SH_RA	brain:	n/a
18	chr4:129805520-129805570	U87	brain:	n/a
19	chr4:129805520-129805570	SK-N-SH	brain:	n/a
20	chr4:129805520-129805570	MCF-7	breast:	n/a
21	chr4:129805520-129805570	GM12878	blood:	n/a
22	chr4:129805520-129805570	GM12891	blood:	n/a
23	chr4:129805520-129805570	ECC-1	luminal epithelium:	n/a
24	chr4:129805520-129805570	Jurkat	blood:	n/a
25	chr4:129805520-129805570	SKMC	muscle:	n/a
26	chr4:129805520-129805570	AoSMC	blood vessel:	n/a
27	chr4:129805520-129805570	BJ	skin:	n/a
28	chr4:129805520-129805570	HNPCEpiC	eye:	n/a
29	chr4:129805520-129805570	PFSK-1	brain:	n/a
30	chr4:129805520-129805570	HEK293	kidney:	embryo
31	chr4:129805520-129805570	BE2_C	brain:	n/a
32	chr4:129805520-129805570	HRCEpiC	kidney:	n/a
33	chr4:129805520-129805570	GM06990	blood:	n/a
34	chr4:129805520-129805570	IMR90	lung:	fetal
35	chr4:129805520-129805570	Hepatocyte	liver:	n/a
36	chr4:129805520-129805570	Caco-2	colon:	n/a
37	chr4:129805520-129805570	NHDF-neo	bronchial:	n/a
38	chr4:129805520-129805570	NB4	blood:	n/a
39	chr4:129805520-129805570	H1-hESC	embryonic stem cell:	embryo
40	chr4:129805520-129805570	AG09309	skin:	n/a
41	chr4:129805520-129805570	HL-60	blood:	n/a
42	chr4:129805520-129805570	RPTEC	kidney:	n/a
43	chr4:129805520-129805570	HCT-116	colon:	n/a
44	chr4:129805520-129805570	AG04449	skin:	fetal
45	chr4:129805520-129805570	HCF	heart:	n/a
46	chr4:129805520-129805570	ovcar-3	ovarian:	n/a
47	chr4:129805520-129805570	SK-N-MC	brain:	n/a
48	chr4:129805520-129805570	MCF10A-Er-Src	breast:	n/a
49	chr4:129805520-129805570	T-47D	breast:	n/a
50	chr4:129805520-129805570	GM19239	blood:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:129796835..129799070-chr4:129823245..129825174,2	K562	blood:
2	chr4:129919094..129920682-chr4:129924284..129926675,2	K562	blood:
3	chr4:129902026..129904676-chr4:129907660..129909341,2	K562	blood:
4	chr4:129918148..129920594-chr4:129924035..129926675,2	K562	blood:
5	chr4:129900386..129903021-chr4:129908411..129910284,2	MCF-7	breast:
6	chr4:129881359..129883041-chr4:129899761..129902463,2	K562	blood:
7	chr4:129869703..129871375-chr4:129874757..129876510,2	K562	blood:
8	chr4:129869703..129871375-chr4:129874757..129876510,2	K562	blood:
9	chr4:129893731..129895681-chr4:129897472..129899242,2	K562	blood:
10	chr4:129731505..129733452-chr4:129799174..129801929,2	MCF-7	breast:
11	chr4:129900386..129903021-chr4:129908411..129910284,2	MCF-7	breast:
12	chr4:129902026..129904676-chr4:129907660..129909341,2	K562	blood:
13	chr4:129863629..129866387-chr4:129870052..129872955,2	K562	blood:
14	chr4:129810865..129812723-chr4:129812841..129815400,2	K562	blood:
15	chr4:129883398..129885861-chr4:129887383..129889705,3	K562	blood:
16	chr4:129885302..129888048-chr4:129911143..129913987,2	K562	blood:
17	chr4:129830344..129833253-chr4:129837741..129840090,2	K562	blood:
18	chr4:129834048..129836614-chr4:129837936..129840499,3	K562	blood:
19	chr4:129834048..129836614-chr4:129837936..129840499,3	K562	blood:
20	chr4:129798920..129801366-chr4:129805840..129808673,2	K562	blood:
21	chr4:129896690..129899278-chr4:129899361..129901444,2	MCF-7	breast:
22	chr4:129896690..129899278-chr4:129899361..129901444,2	MCF-7	breast:
23	chr4:129886935..129889219-chr4:130012773..130015050,2	K562	blood:
24	chr4:129731039..129733137-chr4:129832126..129834778,3	K562	blood:
25	chr4:129810865..129812723-chr4:129812841..129815400,2	K562	blood:
26	chr4:129883398..129885861-chr4:129887383..129889506,2	K562	blood:
27	chr4:129732016..129733966-chr4:129800387..129802773,2	K562	blood:
28	chr4:129834245..129836614-chr4:129838172..129840499,2	K562	blood:
29	chr4:129834245..129836614-chr4:129838172..129840499,2	K562	blood:
30	chr4:129893731..129895681-chr4:129897472..129899242,2	K562	blood:
31	chr4:129919094..129920682-chr4:129924284..129926675,2	K562	blood:
32	chr4:129883398..129885861-chr4:129887383..129889705,3	K562	blood:
33	chr4:129881359..129883041-chr4:129899761..129902463,2	K562	blood:
34	chr4:129802100..129804907-chr4:129805391..129807043,2	K562	blood:
35	chr4:129885302..129888048-chr4:129911143..129913987,2	K562	blood:
36	chr4:129830344..129833253-chr4:129837741..129840090,2	K562	blood:
37	chr4:129802100..129804907-chr4:129805391..129807043,2	K562	blood:
38	chr4:129883398..129885861-chr4:129887383..129889506,2	K562	blood:
39	chr4:129863629..129866387-chr4:129870052..129872955,2	K562	blood:

No data

Variant related genes	Relation type
SCLT1	TF binding region
SCLT1	CpG island
ENSG00000151470	chromatin interactions
ENSG00000151466	chromatin interactions
ENSG00000077684	chromatin interactions

Extended variants
information (count: 4472 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:4472 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529218166	chr4:129801661-129801662	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs574343517	chr4:129801686-129801687	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs1648062	chr4:129801732-129801733	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs577951683	chr4:129801752-129801753	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs142906614	chr4:129801857-129801858	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs35439273	chr4:129801885-129801886	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs187918821	chr4:129801923-129801924	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs76790118	chr4:129801941-129801942	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs147725933	chr4:129801947-129801948	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs537936463	chr4:129801984-129801985	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs7675917	chr4:129802032-129802033	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs191564184	chr4:129802039-129802040	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs34472389	chr4:129802161-129802162	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs142570992	chr4:129802233-129802234	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs114784321	chr4:129802281-129802282	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs184094075	chr4:129802301-129802302	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs146900910	chr4:129802338-129802339	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs199571642	chr4:129802351-129802352	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs374363901	chr4:129802355-129802356	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs147968925	chr4:129802371-129802372	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs563747163	chr4:129802403-129802404	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs564660744	chr4:129802433-129802434	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs528470706	chr4:129802445-129802446	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs555341833	chr4:129802451-129802452	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs141073772	chr4:129802502-129802503	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs547345639	chr4:129802554-129802555	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs116614767	chr4:129802640-129802641	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs188873999	chr4:129802643-129802644	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs547676203	chr4:129802748-129802749	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs541486817	chr4:129802759-129802760	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs17013894	chr4:129802788-129802789	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs72683622	chr4:129802795-129802796	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs181666921	chr4:129802928-129802929	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569498406	chr4:129802929-129802930	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184349620	chr4:129802942-129802943	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs318501	chr4:129802948-129802949	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs570110334	chr4:129802962-129802963	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557595626	chr4:129802968-129802969	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs190230129	chr4:129803067-129803068	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569385041	chr4:129803103-129803104	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs75111318	chr4:129803189-129803190	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs17013895	chr4:129803207-129803208	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs572691250	chr4:129803232-129803233	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs137964602	chr4:129803276-129803277	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532841512	chr4:129803306-129803307	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs552934300	chr4:129803312-129803313	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540153018	chr4:129803353-129803354	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs558420676	chr4:129803372-129803373	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182449376	chr4:129803405-129803406	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs566237753	chr4:129803438-129803439	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
Olfactory neuroblastoma	18408657	CNVD
Developmental delay	21147756	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Gastric cancer	16891809	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1181 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:129779600-129809800	Weak transcription	Small Intestine	intestine
2	chr4:129789400-129811200	Weak transcription	Placenta	Placenta
3	chr4:129793200-129812200	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr4:129793400-129804200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr4:129793600-129804200	Weak transcription	NHLF	lung
6	chr4:129793600-129812000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr4:129793600-129812200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr4:129793600-129812800	Weak transcription	Spleen	Spleen
9	chr4:129793600-129815400	Weak transcription	Fetal Lung	lung
10	chr4:129793600-129816800	Weak transcription	Lung	lung
11	chr4:129793600-129817200	Weak transcription	Psoas Muscle	Psoas
12	chr4:129793600-129825000	Weak transcription	Ovary	ovary
13	chr4:129793800-129811600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr4:129793800-129907200	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr4:129794000-129806200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr4:129794000-129809200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr4:129794000-129813400	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr4:129794000-129814800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr4:129794200-129803400	Weak transcription	Primary neutrophils fromperipheralblood	blood
20	chr4:129794200-129810800	Weak transcription	Fetal Brain Female	brain
21	chr4:129794200-129810800	Weak transcription	Right Ventricle	heart
22	chr4:129794200-129812000	Weak transcription	Stomach Smooth Muscle	stomach
23	chr4:129794200-129815000	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr4:129794200-129816800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr4:129794200-129824800	Weak transcription	Osteobl	bone
26	chr4:129794200-129829400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr4:129794400-129804000	Weak transcription	Fetal Stomach	stomach
28	chr4:129794400-129805600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr4:129794400-129809400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr4:129794400-129811000	Weak transcription	Aorta	Aorta
31	chr4:129794400-129811200	Weak transcription	Fetal Muscle Trunk	muscle
32	chr4:129794400-129811400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr4:129794400-129823800	Weak transcription	Left Ventricle	heart
34	chr4:129794400-129825600	Weak transcription	Gastric	stomach
35	chr4:129794400-129860200	Weak transcription	Thymus	Thymus
36	chr4:129795000-129803400	Weak transcription	Primary B cells from cord blood	blood
37	chr4:129795000-129809400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr4:129795000-129824600	Weak transcription	Rectal Smooth Muscle	rectum
39	chr4:129795200-129805200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr4:129795200-129807800	Weak transcription	Duodenum Mucosa	Duodenum
41	chr4:129795200-129813400	Weak transcription	Primary B cells from peripheral blood	blood
42	chr4:129795400-129809600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr4:129795400-129810200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr4:129795400-129811200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr4:129795600-129802000	Weak transcription	Muscle Satellite Cultured Cells	--
46	chr4:129795800-129803000	Weak transcription	Primary hematopoietic stem cells	blood
47	chr4:129795800-129808800	Weak transcription	HUVEC	blood vessel
48	chr4:129795800-129811800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr4:129795800-129812200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr4:129796000-129809400	Weak transcription	Primary T helper cells fromperipheralblood	blood

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