Variant report

Variant	esv14568
Chromosome Location	chr6:35655914-35656759
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:545)
CpG islands
(count:183)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:545 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:35656514-35657156	K562	blood:	n/a	n/a
2	ATF2	chr6:35655474-35656022	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr6:35656730-35657165	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr6:35655359-35655985	GM12878	blood:	n/a	n/a
5	ATF3	chr6:35656325-35656641	K562	blood:	n/a	n/a
6	BCL3	chr6:35656420-35656955	GM12878	blood:	n/a	chr6:35656423-35656436
7	BCLAF1	chr6:35655528-35656005	GM12878	blood:	n/a	n/a
8	BCLAF1	chr6:35656520-35657014	GM12878	blood:	n/a	n/a
9	BCLAF1	chr6:35656118-35656848	K562	blood:	n/a	chr6:35656126-35656139 chr6:35656279-35656292 chr6:35656423-35656436
10	BCLAF1	chr6:35654962-35656513	GM12878	blood:	n/a	chr6:35656126-35656139 chr6:35656279-35656292 chr6:35656423-35656436
11	BHLHE40	chr6:35655409-35656051	K562	blood:	n/a	n/a
12	BHLHE40	chr6:35656275-35657137	GM12878	blood:	n/a	n/a
13	BHLHE40	chr6:35655793-35656033	GM12878	blood:	n/a	n/a
14	BHLHE40	chr6:35656411-35657186	K562	blood:	n/a	n/a
15	BHLHE40	chr6:35656324-35657088	HepG2	liver:	n/a	n/a
16	CBX3	chr6:35655301-35656559	K562	blood:	n/a	n/a
17	CBX3	chr6:35656712-35657398	K562	blood:	n/a	n/a
18	CCNT2	chr6:35655413-35656980	K562	blood:	n/a	chr6:35656872-35656881
19	CEBPB	chr6:35655152-35655990	GM12878	blood:	n/a	n/a
20	CEBPD	chr6:35656540-35656792	HepG2	liver:	n/a	n/a
21	CEBPD	chr6:35656387-35657199	HepG2	liver:	n/a	n/a
22	CHD1	chr6:35656162-35656700	GM12878	blood:	n/a	n/a
23	CHD2	chr6:35656593-35657155	H1-hESC	embryonic stem cell:	n/a	chr6:35656806-35656813
24	CHD2	chr6:35655782-35655965	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr6:35656450-35657133	K562	blood:	n/a	chr6:35656806-35656813
26	CHD2	chr6:35655748-35655949	Hela-S3	cervix:	n/a	n/a
27	CHD2	chr6:35656709-35657095	HepG2	liver:	n/a	chr6:35656806-35656813
28	CHD2	chr6:35656577-35657037	GM12878	blood:	n/a	chr6:35656806-35656813
29	CHD2	chr6:35656497-35657117	Hela-S3	cervix:	n/a	chr6:35656806-35656813
30	CHD2	chr6:35655759-35655997	GM12878	blood:	n/a	n/a
31	CREB1	chr6:35656566-35657273	H1-hESC	embryonic stem cell:	n/a	n/a
32	CREB1	chr6:35655486-35657266	K562	blood:	n/a	n/a
33	CREB1	chr6:35656253-35657065	A549	lung:	n/a	n/a
34	CREB1	chr6:35655735-35656111	A549	lung:	n/a	n/a
35	CREB1	chr6:35655653-35656078	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTBP2	chr6:35656187-35656832	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr6:35655860-35656010	HepG2	liver:	n/a	n/a
38	CTCF	chr6:35655815-35655923	IMR90	lung:	n/a	n/a
39	CTCF	chr6:35655860-35656010	GM12878	blood:	n/a	n/a
40	CTCF	chr6:35655780-35655930	GM12866	blood:	n/a	n/a
41	CTCF	chr6:35656520-35656670	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr6:35656640-35656790	GM12871	blood:	n/a	n/a
43	CTCF	chr6:35655806-35655946	GM12892	blood:	n/a	n/a
44	CTCF	chr6:35655780-35655930	GM12873	blood:	n/a	n/a
45	CTCF	chr6:35655794-35655969	MCF-7	breast:	n/a	n/a
46	CTCF	chr6:35655820-35655970	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr6:35655840-35655990	GM12868	blood:	n/a	n/a
48	CTCF	chr6:35656300-35656450	GM12873	blood:	n/a	chr6:35656321-35656334
49	CTCF	chr6:35655819-35655926	MCF-7	breast:	n/a	n/a
50	CTCF	chr6:35655780-35655930	HEK293	kidney:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:35656590-35656640	ProgFib	skin:	n/a
2	chr6:35656590-35656640	HL-60	blood:	n/a
3	chr6:35656590-35656640	HRE	kidney:	n/a
4	chr6:35656758-35656808	Hela-S3	cervix:	n/a
5	chr6:35656242-35656292	HRPEpiC	eye:	n/a
6	chr6:35656590-35656640	HIPEpiC	eye:	n/a
7	chr6:35656758-35656808	HAEpiC	amniotic membrane:	n/a
8	chr6:35656242-35656292	Hela-S3	cervix:	n/a
9	chr6:35656242-35656292	MCF-7	breast:	n/a
10	chr6:35656758-35656808	HUVEC	blood vessel:	n/a
11	chr6:35656590-35656640	Caco-2	colon:	n/a
12	chr6:35656590-35656640	GM06990	blood:	n/a
13	chr6:35656242-35656292	HEK293	kidney:	embryo
14	chr6:35656590-35656640	GM12891	blood:	n/a
15	chr6:35656242-35656292	ECC-1	luminal epithelium:	n/a
16	chr6:35656242-35656292	A549	lung:	n/a
17	chr6:35656758-35656808	HPAEpiC	pulmonary alveolar:	n/a
18	chr6:35656242-35656292	K562	blood:	n/a
19	chr6:35656242-35656292	Jurkat	blood:	n/a
20	chr6:35656590-35656640	GM12892	blood:	n/a
21	chr6:35656758-35656808	RPTEC	kidney:	n/a
22	chr6:35656758-35656808	HIPEpiC	eye:	n/a
23	chr6:35656590-35656640	GM12878	blood:	n/a
24	chr6:35656758-35656808	ECC-1	luminal epithelium:	n/a
25	chr6:35656758-35656808	NH-A	brain:	n/a
26	chr6:35656590-35656640	HRPEpiC	eye:	n/a
27	chr6:35656758-35656808	HRPEpiC	eye:	n/a
28	chr6:35656242-35656292	HMEC	breast:	n/a
29	chr6:35656590-35656640	HAEpiC	amniotic membrane:	n/a
30	chr6:35656242-35656292	GM12892	blood:	n/a
31	chr6:35656590-35656640	HCM	heart:	n/a
32	chr6:35656242-35656292	HCM	heart:	n/a
33	chr6:35656590-35656640	SAEC	small airway:	n/a
34	chr6:35656590-35656640	U87	brain:	n/a
35	chr6:35656758-35656808	HEK293	kidney:	embryo
36	chr6:35656758-35656808	SKMC	muscle:	n/a
37	chr6:35656758-35656808	GM12892	blood:	n/a
38	chr6:35656590-35656640	HRCEpiC	kidney:	n/a
39	chr6:35656242-35656292	SKMC	muscle:	n/a
40	chr6:35656242-35656292	HCT-116	colon:	n/a
41	chr6:35656590-35656640	NHDF-neo	bronchial:	n/a
42	chr6:35656758-35656808	HNPCEpiC	eye:	n/a
43	chr6:35656242-35656292	HPAEpiC	pulmonary alveolar:	n/a
44	chr6:35656242-35656292	SK-N-SH_RA	brain:	n/a
45	chr6:35656242-35656292	GM06990	blood:	n/a
46	chr6:35656590-35656640	RPTEC	kidney:	n/a
47	chr6:35656242-35656292	AG09319	gingival:	n/a
48	chr6:35656758-35656808	A549	lung:	n/a
49	chr6:35656590-35656640	ECC-1	luminal epithelium:	n/a
50	chr6:35656590-35656640	NHBE	bronchial:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:35656516..35657052-chr7:39663216..39663813,2	Hela-S3	cervix:
2	chr16:31191242..31191988-chr6:35656271..35657158,2	Hela-S3	cervix:
3	chr6:35511219..35512849-chr6:35653917..35656279,2	MCF-7	breast:
4	chr6:35654156..35657013-chr6:35704693..35707749,4	K562	blood:
5	chr2:10262416..10262948-chr6:35656174..35657022,2	NB4	blood:
6	chr6:35649031..35660636-chr6:35692310..35701686,35	K562	blood:
7	chr6:35464601..35467910-chr6:35655207..35659461,3	K562	blood:
8	chr6:35590466..35592816-chr6:35654896..35656515,2	MCF-7	breast:
9	chr6:35655179..35657311-chr6:35699143..35705251,6	MCF-7	breast:
10	chr15:75660565..75661351-chr6:35656003..35656976,2	Hela-S3	cervix:
11	chr6:35654784..35658036-chr6:35702203..35706321,5	MCF-7	breast:
12	chr6:35649127..35664209-chr6:35693738..35704622,45	K562	blood:
13	chr16:31884910..31885705-chr6:35656392..35657131,2	Hela-S3	cervix:
14	chr6:35630752..35636758-chr6:35653263..35658179,9	K562	blood:
15	chr6:35463571..35465690-chr6:35654249..35656915,2	K562	blood:
16	chr6:35654589..35656249-chr6:35685237..35687965,2	K562	blood:
17	chr6:35654560..35658324-chr6:35694292..35699560,11	MCF-7	breast:
18	chr6:35653875..35657933-chr6:35692950..35698749,12	MCF-7	breast:
19	chr12:121837205..121837751-chr6:35656008..35656965,2	NB4	blood:

No data

Variant related genes	Relation type
FKBP5	TF binding region
FKBP5	CpG island
ENSG00000007866	chromatin interactions
ENSG00000232909	chromatin interactions
ENSG00000185947	chromatin interactions
ENSG00000228559	chromatin interactions
ENSG00000006451	chromatin interactions
ENSG00000140400	chromatin interactions
ENSG00000089053	chromatin interactions
ENSG00000157343	chromatin interactions
ENSG00000265527	chromatin interactions
ENSG00000096060	chromatin interactions
ENSG00000171848	chromatin interactions
ENSG00000089280	chromatin interactions

Extended variants
information (count: 25 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533876911	chr6:35655967-35655968	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs10947564	chr6:35655974-35655975	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs371833025	chr6:35655984-35655985	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs111406566	chr6:35655990-35655991	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs537853796	chr6:35656010-35656011	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs556255180	chr6:35656099-35656100	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs367882511	chr6:35656104-35656105	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs7769449	chr6:35656129-35656130	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs540014174	chr6:35656348-35656349	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
10	rs13215797	chr6:35656431-35656432	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
11	rs573470990	chr6:35656449-35656450	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
12	rs200205569	chr6:35656467-35656468	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
13	rs575946250	chr6:35656473-35656474	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
14	rs540616586	chr6:35656489-35656490	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
15	rs562407722	chr6:35656533-35656534	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
16	rs573910159	chr6:35656550-35656551	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
17	rs9462103	chr6:35656563-35656564	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs147618257	chr6:35656607-35656608	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
19	rs533280354	chr6:35656650-35656651	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
20	rs551145805	chr6:35656687-35656688	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
21	rs560132979	chr6:35656704-35656705	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
22	rs527582958	chr6:35656714-35656715	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
23	rs548961727	chr6:35656722-35656723	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
24	rs550246703	chr6:35656734-35656735	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
25	rs537414337	chr6:35656755-35656756	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
Lung cancer	19153074	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:160 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:35652200-35657000	Active TSS	Psoas Muscle	Psoas
2	chr6:35652800-35656400	Active TSS	Right Atrium	heart
3	chr6:35652800-35656800	Active TSS	Pancreatic Islets	Pancreatic Islet
4	chr6:35652800-35656800	Active TSS	Ovary	ovary
5	chr6:35652800-35656800	Active TSS	Right Ventricle	heart
6	chr6:35652800-35657000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr6:35653400-35656800	Active TSS	Muscle Satellite Cultured Cells	--
8	chr6:35653400-35656800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr6:35653400-35656800	Active TSS	Stomach Smooth Muscle	stomach
10	chr6:35653400-35657000	Active TSS	NHEK	skin
11	chr6:35653600-35656800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr6:35653600-35656800	Active TSS	Primary T helper cells PMA-I stimulated	--
13	chr6:35653600-35656800	Active TSS	Primary T killer naive cells fromperipheralblood	blood
14	chr6:35653600-35656800	Active TSS	HMEC	breast
15	chr6:35653800-35656800	Active TSS	Primary T helper naive cells fromperipheralblood	blood
16	chr6:35653800-35656800	Active TSS	Liver	Liver
17	chr6:35653800-35656800	Active TSS	GM12878-XiMat	blood
18	chr6:35653800-35656800	Active TSS	K562	blood
19	chr6:35653800-35657000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
20	chr6:35653800-35657000	Active TSS	Brain Substantia Nigra	brain
21	chr6:35653800-35657000	Active TSS	Rectal Mucosa Donor 31	rectum
22	chr6:35654000-35657000	Active TSS	Primary T helper cells fromperipheralblood	blood
23	chr6:35654000-35657000	Active TSS	Brain Anterior Caudate	brain
24	chr6:35654000-35657000	Active TSS	Duodenum Smooth Muscle	Duodenum
25	chr6:35654200-35656600	Active TSS	Primary T cells fromperipheralblood	blood
26	chr6:35654200-35656800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr6:35654200-35656800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr6:35654200-35657000	Active TSS	Duodenum Mucosa	Duodenum
29	chr6:35654400-35656000	Flanking Active TSS	Primary B cells from cord blood	blood
30	chr6:35654400-35656000	Active TSS	Fetal Heart	heart
31	chr6:35654400-35656400	Active TSS	Colonic Mucosa	Colon
32	chr6:35654400-35656600	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
33	chr6:35654400-35656800	Active TSS	Aorta	Aorta
34	chr6:35654400-35656800	Active TSS	Fetal Thymus	thymus
35	chr6:35654400-35657000	Active TSS	Breast Myoepithelial Primary Cells	Breast
36	chr6:35654400-35657000	Active TSS	Primary T helper naive cells from peripheral blood	blood
37	chr6:35654400-35657000	Active TSS	Brain Cingulate Gyrus	brain
38	chr6:35654400-35657000	Active TSS	Fetal Adrenal Gland	Adrenal Gland
39	chr6:35654400-35657000	Active TSS	Skeletal Muscle Male	skeletal muscle
40	chr6:35654600-35656200	Active TSS	Primary T killer memory cells from peripheral blood	blood
41	chr6:35654600-35656600	Flanking Active TSS	Primary hematopoietic stem cells	blood
42	chr6:35654600-35657000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr6:35654600-35657000	Active TSS	Brain Angular Gyrus	brain
44	chr6:35654600-35657000	Active TSS	Brain Hippocampus Middle	brain
45	chr6:35654600-35657000	Active TSS	HSMM	muscle
46	chr6:35654600-35657000	Active TSS	HSMMtube	muscle
47	chr6:35654800-35656600	Active TSS	Primary monocytes fromperipheralblood	blood
48	chr6:35654800-35656600	Active TSS	Colon Smooth Muscle	Colon
49	chr6:35654800-35656800	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
50	chr6:35654800-35656800	Active TSS	Monocytes-CD14+_RO01746	blood

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