Variant report

Variant	nsv520053
Chromosome Location	chr6:38154941-38207636
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:436)
CpG islands
(count:184)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:436 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:38187191-38187584	GM12878	blood:	n/a	n/a
2	ATF2	chr6:38187181-38187476	GM12878	blood:	n/a	n/a
3	BCL3	chr6:38182843-38183146	GM12878	blood:	n/a	n/a
4	BCL3	chr6:38183148-38183468	GM12878	blood:	n/a	n/a
5	BHLHE40	chr6:38185658-38185991	K562	blood:	n/a	chr6:38185822-38185835 chr6:38185818-38185839 chr6:38185824-38185833 chr6:38185825-38185834 chr6:38185823-38185832 chr6:38185824-38185833
6	BHLHE40	chr6:38183744-38184107	GM12878	blood:	n/a	chr6:38183964-38183973 chr6:38183964-38183973
7	BHLHE40	chr6:38155175-38155515	K562	blood:	n/a	n/a
8	CBX3	chr6:38165961-38166281	K562	blood:	n/a	n/a
9	CEBPB	chr6:38187234-38187503	IMR90	lung:	n/a	chr6:38187371-38187382
10	CEBPB	chr6:38187222-38187487	A549	lung:	n/a	chr6:38187371-38187382
11	CEBPB	chr6:38188354-38188606	K562	blood:	n/a	chr6:38188484-38188493 chr6:38188482-38188495 chr6:38188483-38188494
12	CEBPB	chr6:38188342-38188650	HepG2	liver:	n/a	chr6:38188484-38188493 chr6:38188482-38188495 chr6:38188483-38188494
13	CEBPB	chr6:38188350-38188588	H1-hESC	embryonic stem cell:	n/a	chr6:38188484-38188493 chr6:38188482-38188495 chr6:38188483-38188494
14	CEBPB	chr6:38187213-38187510	HepG2	liver:	n/a	chr6:38187371-38187382
15	CEBPB	chr6:38181657-38181842	K562	blood:	n/a	n/a
16	CEBPB	chr6:38181640-38181846	HepG2	liver:	n/a	n/a
17	CEBPB	chr6:38181652-38181828	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr6:38181639-38181839	Hela-S3	cervix:	n/a	n/a
19	CREB1	chr6:38187183-38187573	GM12878	blood:	n/a	n/a
20	CREB1	chr6:38180347-38180647	H1-hESC	embryonic stem cell:	n/a	chr6:38180506-38180519
21	CREB1	chr6:38187202-38187628	GM12878	blood:	n/a	n/a
22	CREB1	chr6:38180253-38180773	HepG2	liver:	n/a	chr6:38180506-38180519
23	CTCF	chr6:38155210-38155281	ProgFib	skin:	n/a	chr6:38155257-38155265 chr6:38155252-38155270
24	CTCF	chr6:38202020-38202170	HMF	breast:	n/a	n/a
25	CTCF	chr6:38202020-38202170	GM06990	blood:	n/a	n/a
26	CTCF	chr6:38165960-38166110	HMEC	breast:	n/a	chr6:38166094-38166107
27	CTCF	chr6:38201999-38202297	MCF-7	breast:	n/a	n/a
28	CTCF	chr6:38165966-38166261	K562	blood:	n/a	chr6:38166094-38166107
29	CTCF	chr6:38156578-38156653	K562	blood:	n/a	n/a
30	CTCF	chr6:38202060-38202210	MCF-7	breast:	n/a	n/a
31	CTCF	chr6:38201980-38202130	BE2_C	brain:	n/a	n/a
32	CTCF	chr6:38202077-38202195	NHEK	skin:	n/a	n/a
33	CTCF	chr6:38202073-38202208	GM19239	blood:	n/a	n/a
34	CTCF	chr6:38202040-38202190	GM12875	blood:	n/a	n/a
35	CTCF	chr6:38202040-38202190	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr6:38202020-38202170	HepG2	liver:	n/a	n/a
37	CTCF	chr6:38155160-38155310	HPAF	blood vessel:	n/a	chr6:38155257-38155265 chr6:38155252-38155270
38	CTCF	chr6:38166020-38166170	HBMEC	blood vessel:	n/a	chr6:38166094-38166107
39	CTCF	chr6:38201960-38202110	GM12864	blood:	n/a	n/a
40	CTCF	chr6:38167871-38168026	MCF-7	breast:	n/a	n/a
41	CTCF	chr6:38166040-38166190	WERI-Rb-1	eye:	n/a	chr6:38166094-38166107
42	CTCF	chr6:38155214-38155310	LNCaP	prostate:	n/a	chr6:38155257-38155265 chr6:38155252-38155270
43	CTCF	chr6:38166040-38166181	MCF-7	breast:	n/a	chr6:38166094-38166107
44	CTCF	chr6:38202040-38202190	HRE	kidney:	n/a	n/a
45	CTCF	chr6:38202030-38202165	GM13977	blood:	n/a	n/a
46	CTCF	chr6:38202066-38202198	MCF-7	breast:	n/a	n/a
47	CTCF	chr6:38167924-38168034	HepG2	liver:	n/a	n/a
48	CTCF	chr6:38202020-38202170	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr6:38202092-38202193	MCF-7	breast:	n/a	n/a
50	CTCF	chr6:38155113-38155431	K562	blood:	n/a	chr6:38155257-38155265 chr6:38155252-38155270

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:38160321-38160371	A549	lung:	n/a
2	chr6:38160321-38160371	A549	lung:	n/a
3	chr6:38160321-38160371	HRPEpiC	eye:	n/a
4	chr6:38160321-38160371	Jurkat	blood:	n/a
5	chr6:38202492-38202542	ECC-1	luminal epithelium:	n/a
6	chr6:38160321-38160371	ovcar-3	ovarian:	n/a
7	chr6:38202492-38202542	PrEC	prostate:	n/a
8	chr6:38160321-38160371	LNCaP	prostate:	n/a
9	chr6:38202492-38202542	NB4	blood:	n/a
10	chr6:38160321-38160371	NHBE	bronchial:	n/a
11	chr6:38160321-38160371	NT2-D1	testis:	n/a
12	chr6:38160321-38160371	SKMC	muscle:	n/a
13	chr6:38160321-38160371	NH-A	brain:	n/a
14	chr6:38180047-38180097	HUVEC	blood vessel:	n/a
15	chr6:38202492-38202542	GM19239	blood:	n/a
16	chr6:38202492-38202542	SK-N-SH_RA	brain:	n/a
17	chr6:38160321-38160371	HUVEC	blood vessel:	n/a
18	chr6:38160321-38160371	T-47D	breast:	n/a
19	chr6:38160321-38160371	BE2_C	brain:	n/a
20	chr6:38180047-38180097	ECC-1	luminal epithelium:	n/a
21	chr6:38180047-38180097	HCM	heart:	n/a
22	chr6:38180047-38180097	RPTEC	kidney:	n/a
23	chr6:38180047-38180097	GM19239	blood:	n/a
24	chr6:38180047-38180097	SK-N-SH	brain:	n/a
25	chr6:38180047-38180097	HRPEpiC	eye:	n/a
26	chr6:38180047-38180097	SK-N-MC	brain:	n/a
27	chr6:38180047-38180097	A549	lung:	n/a
28	chr6:38180047-38180097	GM12878	blood:	n/a
29	chr6:38202492-38202542	HCT-116	colon:	n/a
30	chr6:38160321-38160371	HEEpiC	esophagus:	n/a
31	chr6:38180047-38180097	PANC-1	pancreas:	n/a
32	chr6:38160321-38160371	ECC-1	luminal epithelium:	n/a
33	chr6:38202492-38202542	LNCaP	prostate:	n/a
34	chr6:38180047-38180097	AG04450	lung:	fetal
35	chr6:38160321-38160371	AG10803	skin:	n/a
36	chr6:38180047-38180097	GM06990	blood:	n/a
37	chr6:38202492-38202542	HIPEpiC	eye:	n/a
38	chr6:38202492-38202542	SKMC	muscle:	n/a
39	chr6:38202492-38202542	Jurkat	blood:	n/a
40	chr6:38160321-38160371	HRCEpiC	kidney:	n/a
41	chr6:38180047-38180097	Hela-S3	cervix:	n/a
42	chr6:38202492-38202542	T-47D	breast:	n/a
43	chr6:38180047-38180097	HNPCEpiC	eye:	n/a
44	chr6:38180047-38180097	HRE	kidney:	n/a
45	chr6:38180047-38180097	HEK293	kidney:	embryo
46	chr6:38180047-38180097	Caco-2	colon:	n/a
47	chr6:38180047-38180097	HEEpiC	esophagus:	n/a
48	chr6:38202492-38202542	HNPCEpiC	eye:	n/a
49	chr6:38202492-38202542	A549	lung:	n/a
50	chr6:38202492-38202542	NT2-D1	testis:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:38201636..38202567-chr6:38461455..38462314,3	MCF-7	breast:
2	chr6:38116607..38119118-chr6:38160290..38163067,2	K562	blood:
3	chr6:38149475..38152864-chr6:38153550..38156647,3	K562	blood:
4	chr6:38150165..38152745-chr6:38153295..38155930,2	MCF-7	breast:
5	chr6:38185221..38187351-chr6:38192774..38196279,3	K562	blood:
6	chr6:38178185..38180709-chr6:38183811..38185746,2	K562	blood:
7	chr6:38193425..38195567-chr6:38201073..38203728,2	K562	blood:
8	chr6:38188305..38192389-chr6:38192840..38195857,4	K562	blood:
9	chr6:38188305..38192389-chr6:38192840..38195857,4	K562	blood:
10	chr6:38184010..38186134-chr6:38187890..38189397,2	K562	blood:
11	chr6:38143298..38146088-chr6:38153690..38155707,2	K562	blood:
12	chr6:38202043..38202593-chr6:38461632..38462300,2	MCF-7	breast:
13	chr6:38165196..38166057-chr6:38246936..38247494,2	MCF-7	breast:
14	chr6:38195721..38197792-chr6:38201347..38204236,3	MCF-7	breast:
15	chr6:38195721..38197792-chr6:38201347..38204236,3	MCF-7	breast:
16	chr6:38147181..38149521-chr6:38161439..38163786,2	K562	blood:
17	chr6:38184010..38186134-chr6:38187890..38189397,2	K562	blood:
18	chr6:38158880..38161557-chr6:38164282..38166120,2	K562	blood:
19	chr6:38185221..38187351-chr6:38192774..38196279,3	K562	blood:
20	chr6:38163651..38165832-chr6:38213347..38216236,2	K562	blood:
21	chr6:38158880..38161557-chr6:38164282..38166120,2	K562	blood:
22	chr6:38189033..38190926-chr6:38201361..38202956,2	K562	blood:
23	chr6:38193425..38195567-chr6:38201073..38203728,2	K562	blood:
24	chr6:38206376..38209309-chr6:38213456..38216223,2	MCF-7	breast:
25	chr6:38178185..38180709-chr6:38183811..38185746,2	K562	blood:
26	chr6:38189033..38190926-chr6:38201361..38202956,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000200706	TF binding region
ENSG00000200706	CpG island

Extended variants
information (count: 1871 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1871 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11757846	chr6:38154941-38154942	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs544203707	chr6:38154968-38154969	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs183903304	chr6:38154975-38154976	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs189427061	chr6:38154978-38154979	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs546697876	chr6:38154995-38154996	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192684308	chr6:38155008-38155009	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs368697050	chr6:38155064-38155065	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560461172	chr6:38155083-38155084	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs529132318	chr6:38155159-38155160	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs184352855	chr6:38155173-38155174	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs139453669	chr6:38155244-38155245	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs569391366	chr6:38155245-38155246	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs531802152	chr6:38155292-38155293	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs114768064	chr6:38155304-38155305	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs571599509	chr6:38155352-38155353	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs190019471	chr6:38155371-38155372	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs10807190	chr6:38155404-38155405	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs541657046	chr6:38155405-38155406	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs149659653	chr6:38155473-38155474	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs181183152	chr6:38155522-38155523	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs376829095	chr6:38155535-38155536	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs574366668	chr6:38155546-38155547	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs186270669	chr6:38155565-38155566	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs189983841	chr6:38155577-38155578	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs544021154	chr6:38155585-38155586	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs557823420	chr6:38155600-38155601	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs180807905	chr6:38155660-38155661	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs117616309	chr6:38155675-38155676	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs144451399	chr6:38155718-38155719	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs185268084	chr6:38155719-38155720	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs9470819	chr6:38155725-38155726	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs9470820	chr6:38155731-38155732	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs562626417	chr6:38155746-38155747	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs531531454	chr6:38155751-38155752	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs190719600	chr6:38155763-38155764	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs139159065	chr6:38155784-38155785	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs545630271	chr6:38155843-38155844	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs144045150	chr6:38155900-38155901	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547350706	chr6:38155927-38155928	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564015934	chr6:38155951-38155952	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs567629304	chr6:38155952-38155953	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs183281483	chr6:38155961-38155962	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556433871	chr6:38155969-38155970	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185723915	chr6:38156010-38156011	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs539206423	chr6:38156058-38156059	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs535857466	chr6:38156064-38156065	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs191666874	chr6:38156131-38156132	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs533080127	chr6:38156225-38156226	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539818594	chr6:38156242-38156243	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs539865298	chr6:38156249-38156250	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Osteosarcoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Lung cancer	19153074	CNVD
Ovarian cancer	21720365	CNVD
Melanoma	21693616	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Breast cancer	16397240	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	17603634	CNVD

Chromatin state (count:809 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:38121000-38159600	Weak transcription	Primary T cells fromperipheralblood	blood
2	chr6:38123400-38155400	Weak transcription	Aorta	Aorta
3	chr6:38123400-38157000	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr6:38123400-38176800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr6:38131800-38167800	Weak transcription	Right Atrium	heart
6	chr6:38133600-38160400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr6:38133600-38164000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr6:38136000-38159800	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr6:38136800-38156000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr6:38138600-38169400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr6:38141600-38166200	Weak transcription	Left Ventricle	heart
12	chr6:38141800-38168000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr6:38142200-38155400	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr6:38142800-38162000	Weak transcription	Adipose Nuclei	Adipose
15	chr6:38143200-38159200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr6:38143200-38161200	Weak transcription	Placenta	Placenta
17	chr6:38143600-38162400	Weak transcription	Right Ventricle	heart
18	chr6:38143600-38177200	Weak transcription	Ovary	ovary
19	chr6:38144000-38159200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr6:38144000-38161400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr6:38144000-38161400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr6:38144000-38161600	Weak transcription	Thymus	Thymus
23	chr6:38144200-38155600	Weak transcription	Spleen	Spleen
24	chr6:38145200-38155600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr6:38145200-38156400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr6:38145200-38163400	Weak transcription	Colonic Mucosa	Colon
27	chr6:38145600-38155000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr6:38145600-38155200	Weak transcription	Fetal Muscle Leg	muscle
29	chr6:38145800-38159600	Weak transcription	Fetal Intestine Large	intestine
30	chr6:38145800-38159800	Weak transcription	Liver	Liver
31	chr6:38146000-38162400	Weak transcription	Pancreas	Pancrea
32	chr6:38146200-38155000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr6:38146400-38155000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr6:38146400-38155000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr6:38146400-38161600	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr6:38146400-38162400	Weak transcription	Gastric	stomach
37	chr6:38146600-38159400	Weak transcription	Esophagus	oesophagus
38	chr6:38146600-38160800	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr6:38146600-38162400	Weak transcription	Duodenum Mucosa	Duodenum
40	chr6:38147400-38180400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr6:38148000-38159600	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr6:38148200-38162200	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr6:38148400-38155000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr6:38150600-38155200	Weak transcription	Primary T cells from cord blood	blood
45	chr6:38151800-38155800	Enhancers	Brain Angular Gyrus	brain
46	chr6:38151800-38155800	Enhancers	Brain Anterior Caudate	brain
47	chr6:38152000-38156000	Enhancers	Brain Substantia Nigra	brain
48	chr6:38152000-38161200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr6:38152000-38166600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
50	chr6:38152200-38156000	Enhancers	Brain Germinal Matrix	brain

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