Variant report

Variant	nsv965713
Chromosome Location	chr6:34708188-34713851
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	chr6:34708281-34708419	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:34709883-34710222	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:34713147-34714396	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:34712925-34713484	K562	blood:	n/a	n/a
5	ATF1	chr6:34712995-34713537	K562	blood:	n/a	n/a
6	ATF3	chr6:34713058-34713580	K562	blood:	n/a	n/a
7	BHLHE40	chr6:34708114-34708531	K562	blood:	n/a	n/a
8	BHLHE40	chr6:34708230-34708442	HepG2	liver:	n/a	n/a
9	BHLHE40	chr6:34713058-34713476	K562	blood:	n/a	n/a
10	BRCA1	chr6:34708223-34708553	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr6:34712933-34713564	K562	blood:	n/a	n/a
12	CCNT2	chr6:34713189-34713519	K562	blood:	n/a	n/a
13	CCNT2	chr6:34711877-34711891	K562	blood:	n/a	n/a
14	CEBPB	chr6:34708225-34708526	A549	lung:	n/a	chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708378-34708389 chr6:34708380-34708391 chr6:34708380-34708389
15	CEBPB	chr6:34712989-34713445	K562	blood:	n/a	n/a
16	CEBPB	chr6:34708280-34708510	IMR90	lung:	n/a	chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708378-34708389 chr6:34708380-34708391 chr6:34708380-34708389
17	CEBPB	chr6:34708209-34708551	MCF-7	breast:	n/a	chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708378-34708389 chr6:34708380-34708391 chr6:34708380-34708389
18	CEBPB	chr6:34708280-34708505	H1-hESC	embryonic stem cell:	n/a	chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708378-34708389 chr6:34708380-34708391 chr6:34708380-34708389
19	CEBPB	chr6:34709955-34710097	A549	lung:	n/a	chr6:34710057-34710068
20	CEBPB	chr6:34708222-34708519	HepG2	liver:	n/a	chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708378-34708389 chr6:34708380-34708391 chr6:34708380-34708389
21	CEBPB	chr6:34708193-34708564	HepG2	liver:	n/a	chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708378-34708389 chr6:34708380-34708391 chr6:34708380-34708389
22	CEBPB	chr6:34708196-34708577	K562	blood:	n/a	chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708378-34708389 chr6:34708380-34708391 chr6:34708380-34708389
23	CEBPB	chr6:34708108-34708643	K562	blood:	n/a	chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708378-34708389 chr6:34708380-34708391 chr6:34708380-34708389
24	CEBPB	chr6:34708243-34708469	K562	blood:	n/a	chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708378-34708389 chr6:34708380-34708391 chr6:34708380-34708389
25	CEBPB	chr6:34709928-34710240	HepG2	liver:	n/a	chr6:34710057-34710068
26	CEBPB	chr6:34708197-34708579	HepG2	liver:	n/a	chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708378-34708389 chr6:34708380-34708391 chr6:34708380-34708389
27	CEBPB	chr6:34708157-34708498	HepG2	liver:	n/a	chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708378-34708389 chr6:34708380-34708391 chr6:34708380-34708389
28	CEBPB	chr6:34708167-34708601	Hela-S3	cervix:	n/a	chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708380-34708389 chr6:34708378-34708389 chr6:34708380-34708391 chr6:34708380-34708389
29	CEBPD	chr6:34712770-34713586	K562	blood:	n/a	n/a
30	CUX1	chr6:34712966-34713454	K562	blood:	n/a	n/a
31	E2F4	chr6:34708273-34708423	MCF10A-Er-Src	breast:	n/a	n/a
32	EBF1	chr6:34711463-34711642	GM12878	blood:	n/a	n/a
33	EBF1	chr6:34711483-34711717	GM12878	blood:	n/a	n/a
34	EGR1	chr6:34713025-34713499	K562	blood:	n/a	n/a
35	EGR1	chr6:34712981-34713532	K562	blood:	n/a	n/a
36	ELF1	chr6:34713408-34714126	MCF-7	breast:	n/a	n/a
37	ELF1	chr6:34713538-34714039	MCF-7	breast:	n/a	n/a
38	EP300	chr6:34712968-34713497	K562	blood:	n/a	chr6:34713362-34713371
39	FOS	chr6:34713198-34713540	MCF10A-Er-Src	breast:	n/a	chr6:34713359-34713370 chr6:34713362-34713371 chr6:34713364-34713371 chr6:34713361-34713373
40	FOS	chr6:34713112-34713543	K562	blood:	n/a	chr6:34713359-34713370 chr6:34713362-34713371 chr6:34713364-34713371 chr6:34713361-34713373
41	FOS	chr6:34707669-34708535	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr6:34708187-34708565	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr6:34707707-34708577	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr6:34709925-34710249	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr6:34713198-34713547	MCF10A-Er-Src	breast:	n/a	chr6:34713359-34713370 chr6:34713362-34713371 chr6:34713364-34713371 chr6:34713361-34713373
46	FOS	chr6:34709850-34710250	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr6:34713240-34713515	MCF10A-Er-Src	breast:	n/a	chr6:34713359-34713370 chr6:34713362-34713371 chr6:34713364-34713371 chr6:34713361-34713373
48	FOS	chr6:34713191-34713515	MCF10A-Er-Src	breast:	n/a	chr6:34713359-34713370 chr6:34713362-34713371 chr6:34713364-34713371 chr6:34713361-34713373
49	FOS	chr6:34709926-34710203	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr6:34708191-34708502	MCF10A-Er-Src	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:34711953..34714210-chr6:34722946..34726652,3	K562	blood:
2	chr6:34707099..34709785-chr6:34713149..34715872,2	K562	blood:
3	chr6:34708225..34709906-chr6:34758782..34761089,2	MCF-7	breast:
4	chr6:34712695..34714463-chr6:34723596..34725137,2	MCF-7	breast:
5	chr6:34713112..34714744-chr6:34728866..34731406,2	K562	blood:
6	chr6:34707078..34708583-chr6:34711882..34714603,2	MCF-7	breast:
7	chr6:34706320..34708599-chr6:34713149..34715491,2	K562	blood:
8	chr6:34709940..34711491-chr6:34711698..34713387,2	K562	blood:
9	chr6:34707099..34709785-chr6:34713149..34715872,2	K562	blood:
10	chr6:34706864..34709056-chr6:34722827..34726268,3	K562	blood:
11	chr6:34665132..34667717-chr6:34706629..34708944,2	MCF-7	breast:
12	chr6:34706320..34708599-chr6:34713149..34715491,2	K562	blood:
13	chr6:34712098..34715933-chr6:34757940..34761251,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000217130	TF binding region
ENSG00000124562	chromatin interactions
ENSG00000217130	chromatin interactions
ENSG00000065060	chromatin interactions

Extended variants
information (count: 235 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:235 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538458764	chr6:34708208-34708209	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs375240935	chr6:34708209-34708210	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs34884826	chr6:34708211-34708212	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs532179668	chr6:34708270-34708271	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs184683531	chr6:34708296-34708297	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs566023801	chr6:34708355-34708356	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs529902494	chr6:34708366-34708367	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs548037200	chr6:34708388-34708389	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs569834762	chr6:34708406-34708407	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs535773843	chr6:34708411-34708412	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs112120872	chr6:34708443-34708444	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs10947526	chr6:34708448-34708449	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
13	rs147954910	chr6:34708450-34708451	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs534987662	chr6:34708451-34708452	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs537926673	chr6:34708457-34708458	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs10947527	chr6:34708474-34708475	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs71542490	chr6:34708476-34708477	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
18	rs10947528	chr6:34708483-34708484	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs554041009	chr6:34708509-34708510	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs572448179	chr6:34708537-34708538	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs375984747	chr6:34708552-34708553	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs555575529	chr6:34708610-34708611	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs554835198	chr6:34708622-34708623	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs147806317	chr6:34708637-34708638	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs369322490	chr6:34708675-34708676	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs140158165	chr6:34708737-34708738	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs190015400	chr6:34708748-34708749	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs150302093	chr6:34708758-34708759	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs181762149	chr6:34708761-34708762	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs559397518	chr6:34708769-34708770	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs2764200	chr6:34708775-34708776	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs548488707	chr6:34708786-34708787	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs186021061	chr6:34708802-34708803	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs149114141	chr6:34708803-34708804	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs2764201	chr6:34708850-34708851	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs2764202	chr6:34708896-34708897	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs2764203	chr6:34708901-34708902	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs373207123	chr6:34708906-34708907	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs2814963	chr6:34708908-34708909	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs536509706	chr6:34708914-34708915	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs555276926	chr6:34708955-34708956	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs141783879	chr6:34709047-34709048	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs536079504	chr6:34709155-34709156	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs368391736	chr6:34709156-34709157	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs544041472	chr6:34709158-34709159	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs75617380	chr6:34709168-34709169	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs74810280	chr6:34709169-34709170	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs79496941	chr6:34709170-34709171	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs575528539	chr6:34709248-34709249	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs558673398	chr6:34709262-34709263	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Esophageal adenocarcinoma	18820669	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
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	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
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:92 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34698000-34714000	Weak transcription	Esophagus	oesophagus
2	chr6:34699800-34712200	Weak transcription	Stomach Mucosa	stomach
3	chr6:34706400-34712800	Enhancers	HepG2	liver
4	chr6:34707000-34708600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr6:34707000-34709000	Enhancers	Fetal Intestine Large	intestine
6	chr6:34707000-34709000	Enhancers	K562	blood
7	chr6:34707400-34708400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr6:34707400-34708400	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr6:34707400-34708600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:34707400-34709000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr6:34707600-34708600	Enhancers	Fetal Intestine Small	intestine
12	chr6:34707600-34709000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr6:34707600-34709000	Enhancers	NHEK	skin
14	chr6:34707800-34708800	Weak transcription	Small Intestine	intestine
15	chr6:34708000-34708200	Enhancers	Hela-S3	cervix
16	chr6:34708000-34708400	Enhancers	A549	lung
17	chr6:34708200-34708400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr6:34708200-34708600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr6:34708200-34708600	Enhancers	Liver	Liver
20	chr6:34708200-34708600	Enhancers	Duodenum Mucosa	Duodenum
21	chr6:34708200-34708600	Flanking Active TSS	Hela-S3	cervix
22	chr6:34708400-34708600	Enhancers	Rectal Mucosa Donor 29	rectum
23	chr6:34708400-34712800	Weak transcription	A549	lung
24	chr6:34708600-34711200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr6:34708600-34712200	Weak transcription	Duodenum Mucosa	Duodenum
26	chr6:34708600-34712200	Weak transcription	Fetal Intestine Small	intestine
27	chr6:34708600-34712600	Weak transcription	Hela-S3	cervix
28	chr6:34708600-34713000	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr6:34708600-34713200	Weak transcription	Liver	Liver
30	chr6:34708800-34709400	Enhancers	Small Intestine	intestine
31	chr6:34708800-34711400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr6:34709000-34711200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr6:34709000-34711200	Weak transcription	NHEK	skin
34	chr6:34709000-34711600	Weak transcription	Fetal Intestine Large	intestine
35	chr6:34709000-34712800	Weak transcription	K562	blood
36	chr6:34709400-34712200	Weak transcription	Small Intestine	intestine
37	chr6:34711200-34712800	Enhancers	NHEK	skin
38	chr6:34711200-34713200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr6:34711200-34713200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr6:34711400-34711600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr6:34711400-34714600	Enhancers	Placenta	Placenta
42	chr6:34711600-34712000	Enhancers	Placenta Amnion	Placenta Amnion
43	chr6:34711600-34712600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr6:34711600-34715400	Enhancers	Fetal Intestine Large	intestine
45	chr6:34712000-34712400	Weak transcription	Placenta Amnion	Placenta Amnion
46	chr6:34712200-34713000	Enhancers	Duodenum Mucosa	Duodenum
47	chr6:34712200-34713000	Enhancers	Small Intestine	intestine
48	chr6:34712200-34713000	Enhancers	Stomach Mucosa	stomach
49	chr6:34712200-34714800	Enhancers	Fetal Intestine Small	intestine
50	chr6:34712400-34714400	Enhancers	Placenta Amnion	Placenta Amnion

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