Variant report

Variant	nsv969389
Chromosome Location	chr6:34542883-34545751
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	BCL3	chr6:34543140-34543668	K562	blood:	n/a	chr6:34543350-34543359
2	CTCF	chr6:34543138-34543332	GM12878	blood:	n/a	n/a
3	CTCF	chr6:34543200-34543350	GM12872	blood:	n/a	n/a
4	CTCF	chr6:34543182-34543278	GM12891	blood:	n/a	n/a
5	CTCF	chr6:34543280-34543430	SAEC	small airway:	n/a	chr6:34543353-34543366
6	CTCF	chr6:34543212-34543258	GM12878	blood:	n/a	n/a
7	CTCF	chr6:34543300-34543450	GM12873	blood:	n/a	chr6:34543353-34543366
8	CTCF	chr6:34543317-34543322	Hela-S3	cervix:	n/a	n/a
9	CTCF	chr6:34543163-34543382	K562	blood:	n/a	chr6:34543353-34543366
10	CTCF	chr6:34543206-34543278	MCF-7	breast:	n/a	n/a
11	CTCF	chr6:34543219-34543269	Hela-S3	cervix:	n/a	n/a
12	CTCF	chr6:34543200-34543350	Caco-2	colon:	n/a	n/a
13	CTCF	chr6:34543057-34543395	H1-hESC	embryonic stem cell:	n/a	chr6:34543353-34543366
14	CTCF	chr6:34543169-34543354	HepG2	liver:	n/a	n/a
15	CTCF	chr6:34543317-34543398	K562	blood:	n/a	chr6:34543353-34543366
16	CTCF	chr6:34543166-34543301	GM19239	blood:	n/a	n/a
17	CTCF	chr6:34543325-34543329	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr6:34543350-34543390	Hela-S3	cervix:	n/a	chr6:34543353-34543366
19	CTCF	chr6:34543120-34543270	GM12875	blood:	n/a	n/a
20	CTCF	chr6:34543189-34543328	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr6:34543140-34543290	HEK293	kidney:	n/a	n/a
22	CTCF	chr6:34543109-34543610	K562	blood:	n/a	chr6:34543451-34543459 chr6:34543353-34543366
23	CTCF	chr6:34543080-34543230	WERI-Rb-1	eye:	n/a	n/a
24	CTCF	chr6:34543180-34543506	K562	blood:	n/a	chr6:34543451-34543459 chr6:34543353-34543366
25	CTCF	chr6:34543280-34543430	AG09309	skin:	n/a	chr6:34543353-34543366
26	CTCF	chr6:34543280-34543430	K562	blood:	n/a	chr6:34543353-34543366
27	CTCF	chr6:34543200-34543350	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr6:34543186-34543290	GM12892	blood:	n/a	n/a
29	CTCF	chr6:34543240-34543390	HRE	kidney:	n/a	chr6:34543353-34543366
30	CTCF	chr6:34543176-34543413	K562	blood:	n/a	chr6:34543353-34543366
31	CTCF	chr6:34543220-34543370	HEK293	kidney:	n/a	chr6:34543353-34543366
32	CTCF	chr6:34543280-34543430	HBMEC	blood vessel:	n/a	chr6:34543353-34543366
33	CTCF	chr6:34543930-34543974	GM10248	blood:	n/a	n/a
34	CTCF	chr6:34543120-34543270	HepG2	liver:	n/a	n/a
35	CTCFL	chr6:34543241-34543424	K562	blood:	n/a	n/a
36	EGR1	chr6:34543168-34543578	K562	blood:	n/a	chr6:34543322-34543335
37	EGR1	chr6:34543123-34543510	K562	blood:	n/a	chr6:34543322-34543335
38	EGR1	chr6:34543078-34543454	H1-hESC	embryonic stem cell:	n/a	chr6:34543322-34543335
39	ELF1	chr6:34543064-34543442	K562	blood:	n/a	n/a
40	ELF1	chr6:34543139-34543455	K562	blood:	n/a	n/a
41	FOSL2	chr6:34543846-34544468	HepG2	liver:	n/a	n/a
42	FOSL2	chr6:34542565-34543399	HepG2	liver:	n/a	n/a
43	GABPA	chr6:34543028-34543404	K562	blood:	n/a	n/a
44	GTF2F1	chr6:34543236-34543237	H1-hESC	embryonic stem cell:	n/a	n/a
45	IRF1	chr6:34544321-34544690	K562	blood:	n/a	chr6:34544504-34544517 chr6:34544502-34544516 chr6:34544502-34544516 chr6:34544504-34544518 chr6:34544503-34544517 chr6:34544503-34544514 chr6:34544504-34544515 chr6:34544503-34544516 chr6:34544504-34544517 chr6:34544503-34544513 chr6:34544504-34544517
46	IRF1	chr6:34544368-34544652	K562	blood:	n/a	chr6:34544504-34544517 chr6:34544502-34544516 chr6:34544502-34544516 chr6:34544504-34544518 chr6:34544503-34544517 chr6:34544503-34544514 chr6:34544504-34544515 chr6:34544503-34544516 chr6:34544504-34544517 chr6:34544503-34544513 chr6:34544504-34544517
47	MAZ	chr6:34543141-34543281	Hela-S3	cervix:	n/a	n/a
48	MAZ	chr6:34543175-34543492	K562	blood:	n/a	n/a
49	POLR2A	chr6:34543782-34544957	GM12878	blood:	n/a	n/a
50	POLR2A	chr6:34542912-34543298	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:34543055-34543105	H1-hESC	embryonic stem cell:	embryo
2	chr6:34543055-34543105	T-47D	breast:	n/a
3	chr6:34543055-34543105	GM19239	blood:	n/a
4	chr6:34543055-34543105	MCF-7	breast:	n/a
5	chr6:34543055-34543105	GM12878	blood:	n/a
6	chr6:34543055-34543105	GM06990	blood:	n/a
7	chr6:34543055-34543105	PrEC	prostate:	n/a
8	chr6:34543055-34543105	SK-N-SH_RA	brain:	n/a
9	chr6:34543055-34543105	AoSMC	blood vessel:	n/a
10	chr6:34543055-34543105	AG04449	skin:	fetal
11	chr6:34543055-34543105	Hepatocyte	liver:	n/a
12	chr6:34543055-34543105	BJ	skin:	n/a
13	chr6:34543055-34543105	IMR90	lung:	fetal
14	chr6:34543055-34543105	ovcar-3	ovarian:	n/a
15	chr6:34543055-34543105	PFSK-1	brain:	n/a
16	chr6:34543055-34543105	HCT-116	colon:	n/a
17	chr6:34543055-34543105	BE2_C	brain:	n/a
18	chr6:34543055-34543105	SK-N-SH	brain:	n/a
19	chr6:34543055-34543105	Jurkat	blood:	n/a
20	chr6:34543055-34543105	HIPEpiC	eye:	n/a
21	chr6:34543055-34543105	HAEpiC	amniotic membrane:	n/a
22	chr6:34543055-34543105	NHBE	bronchial:	n/a
23	chr6:34543055-34543105	NT2-D1	testis:	n/a
24	chr6:34543055-34543105	MCF10A-Er-Src	breast:	n/a
25	chr6:34543055-34543105	HCF	heart:	n/a
26	chr6:34543055-34543105	AG09309	skin:	n/a
27	chr6:34543055-34543105	Caco-2	colon:	n/a
28	chr6:34543055-34543105	HRPEpiC	eye:	n/a
29	chr6:34543055-34543105	CMK	blood:	n/a
30	chr6:34543055-34543105	HEEpiC	esophagus:	n/a
31	chr6:34543055-34543105	RPTEC	kidney:	n/a
32	chr6:34543055-34543105	LNCaP	prostate:	n/a
33	chr6:34543055-34543105	AG09319	gingival:	n/a
34	chr6:34543055-34543105	PANC-1	pancreas:	n/a
35	chr6:34543055-34543105	K562	blood:	n/a
36	chr6:34543055-34543105	AG10803	skin:	n/a
37	chr6:34543055-34543105	ProgFib	skin:	n/a
38	chr6:34543055-34543105	HRCEpiC	kidney:	n/a
39	chr6:34543055-34543105	HL-60	blood:	n/a
40	chr6:34543055-34543105	NH-A	brain:	n/a
41	chr6:34543055-34543105	HPAEpiC	pulmonary alveolar:	n/a
42	chr6:34543055-34543105	GM12892	blood:	n/a
43	chr6:34543055-34543105	SKMC	muscle:	n/a
44	chr6:34543055-34543105	HNPCEpiC	eye:	n/a
45	chr6:34543055-34543105	AG04450	lung:	fetal
46	chr6:34543055-34543105	Hela-S3	cervix:	n/a
47	chr6:34543055-34543105	NHDF-neo	bronchial:	n/a
48	chr6:34543055-34543105	HRE	kidney:	n/a
49	chr6:34543055-34543105	HCPEpiC	choroid plexus:	n/a
50	chr6:34543055-34543105	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:34538087..34543232-chr6:34543693..34548004,8	K562	blood:
2	chr6:34535124..34537027-chr6:34540257..34543237,2	K562	blood:
3	chr6:34205425..34208316-chr6:34542456..34544168,2	K562	blood:
4	chr6:34532465..34535112-chr6:34540040..34542974,2	K562	blood:
5	chr6:34528409..34535112-chr6:34539790..34543716,10	K562	blood:
6	chr6:34544544..34547164-chr6:34547916..34551672,4	K562	blood:
7	chr6:34529351..34531637-chr6:34540105..34542943,4	K562	blood:
8	chr6:34522370..34525112-chr6:34541822..34544372,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000196114	TF binding region
ENSG00000196114	CpG island
ENSG00000137309	chromatin interactions
ENSG00000124664	chromatin interactions
ENSG00000196114	chromatin interactions

Extended variants
information (count: 136 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:136 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368334376	chr6:34542900-34542901	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs113989557	chr6:34542906-34542907	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs144886459	chr6:34542926-34542927	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs567122792	chr6:34542930-34542931	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs537654465	chr6:34542934-34542935	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs146101231	chr6:34542976-34542977	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs112391007	chr6:34542983-34542984	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs141291894	chr6:34543015-34543016	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs568278918	chr6:34543016-34543017	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs371306751	chr6:34543055-34543056	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs184011485	chr6:34543056-34543057	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs116611404	chr6:34543098-34543099	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs555788434	chr6:34543105-34543106	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs35569925	chr6:34543156-34543157	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs574244266	chr6:34543172-34543173	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs11397210	chr6:34543182-34543183	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs563357166	chr6:34543207-34543208	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs374510426	chr6:34543216-34543217	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs552530958	chr6:34543289-34543290	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs562539103	chr6:34543303-34543304	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs188948278	chr6:34543333-34543334	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs114055222	chr6:34543334-34543335	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs544807814	chr6:34543355-34543356	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs148124051	chr6:34543360-34543361	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs527345943	chr6:34543444-34543445	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs542862937	chr6:34543452-34543453	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs560859997	chr6:34543453-34543454	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs531369655	chr6:34543499-34543500	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs549589405	chr6:34543520-34543521	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs571137052	chr6:34543532-34543533	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs533449941	chr6:34543533-34543534	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs190844260	chr6:34543536-34543537	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs141884207	chr6:34543554-34543555	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs533949376	chr6:34543569-34543570	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs556059668	chr6:34543573-34543574	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs567979608	chr6:34543607-34543608	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs182614265	chr6:34543618-34543619	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs576376999	chr6:34543631-34543632	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs76449706	chr6:34543666-34543667	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs373458036	chr6:34543859-34543860	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs76008675	chr6:34543861-34543862	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs578234441	chr6:34543862-34543863	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs545086451	chr6:34543863-34543864	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs533762984	chr6:34543864-34543865	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs377224541	chr6:34543865-34543866	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs542276147	chr6:34543866-34543867	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs560822773	chr6:34543869-34543870	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs186641121	chr6:34543878-34543879	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs543346426	chr6:34543891-34543892	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs564729483	chr6:34543923-34543924	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34528800-34551400	Weak transcription	Right Atrium	heart
2	chr6:34530200-34548000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:34532800-34548200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr6:34535200-34544200	Weak transcription	Spleen	Spleen
5	chr6:34535600-34563200	Weak transcription	A549	lung
6	chr6:34536400-34545600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr6:34536800-34554400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr6:34536800-34556600	Weak transcription	Hela-S3	cervix
9	chr6:34537400-34552800	Weak transcription	Fetal Intestine Large	intestine
10	chr6:34538000-34544000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr6:34538000-34555400	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr6:34538800-34550600	Weak transcription	Esophagus	oesophagus
13	chr6:34538800-34552600	Weak transcription	Right Ventricle	heart
14	chr6:34539600-34552800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr6:34540200-34548800	Weak transcription	Fetal Muscle Leg	muscle
16	chr6:34540800-34554000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr6:34541400-34548600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr6:34541600-34553200	Weak transcription	Lung	lung
19	chr6:34541800-34553400	Weak transcription	HepG2	liver
20	chr6:34542000-34543200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
21	chr6:34542000-34544400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr6:34542000-34553000	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr6:34542200-34543200	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr6:34542200-34543200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr6:34542200-34543400	Enhancers	K562	blood
26	chr6:34542200-34544000	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr6:34542200-34544200	Enhancers	H1 Cell Line	embryonic stem cell
28	chr6:34542200-34544200	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr6:34542200-34544400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr6:34542200-34548600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr6:34542200-34555400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr6:34542400-34553800	Weak transcription	Liver	Liver
33	chr6:34542600-34543200	Enhancers	H9 Cell Line	embryonic stem cell
34	chr6:34542600-34545800	Weak transcription	Adipose Nuclei	Adipose
35	chr6:34542800-34543400	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr6:34542800-34543400	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr6:34543000-34543200	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr6:34543200-34543600	Enhancers	Placenta	Placenta
39	chr6:34543200-34544000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
40	chr6:34543200-34544000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr6:34543200-34548600	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr6:34543200-34548600	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr6:34543200-34549000	Weak transcription	Fetal Intestine Small	intestine
44	chr6:34543200-34552200	Weak transcription	HUES6 Cell Line	embryonic stem cell
45	chr6:34543400-34545200	Weak transcription	K562	blood
46	chr6:34543600-34544000	Weak transcription	Placenta	Placenta
47	chr6:34543800-34544000	Weak transcription	Pancreas	Pancrea
48	chr6:34544000-34544200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
49	chr6:34544000-34544200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr6:34544000-34544200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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