Variant report

Variant	nsv965717
Chromosome Location	chr6:35437464-35438661
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:32)
LncRNA
region (count:0)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

No data

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:26045293..26047313-chr6:35435617..35437589,2	MCF-7	breast:
2	chr11:2397606..2400001-chr6:35434655..35437647,2	K562	blood:
3	chr12:54366608..54368151-chr6:35435475..35437868,2	MCF-7	breast:
4	chr20:46247769..46250041-chr6:35436696..35439352,2	MCF-7	breast:
5	chr6:35253934..35256378-chr6:35438296..35440191,2	K562	blood:
6	chr6:35308405..35313609-chr6:35434054..35440248,12	K562	blood:
7	chr6:35334952..35336985-chr6:35437820..35439683,2	MCF-7	breast:
8	chr6:35257372..35267871-chr6:35433266..35439192,25	K562	blood:
9	chr6:35437115..35437843-chr6:109415713..109416328,2	Hela-S3	cervix:
10	chr6:35436419..35438425-chr6:35888772..35891148,2	K562	blood:
11	chr6:35261657..35264844-chr6:35438190..35440165,4	MCF-7	breast:
12	chr6:35308378..35313609-chr6:35433550..35439145,12	K562	blood:
13	chr6:35226066..35229330-chr6:35434346..35438215,4	K562	blood:
14	chr6:35259383..35261485-chr6:35435927..35437799,2	MCF-7	breast:
15	chr6:35419539..35422466-chr6:35438622..35441201,2	MCF-7	breast:
16	chr6:35438538..35440763-chr6:35753826..35756739,2	K562	blood:
17	chr6:35418617..35424875-chr6:35434196..35438070,12	MCF-7	breast:
18	chr6:35226330..35228825-chr6:35434969..35437843,3	MCF-7	breast:
19	chr6:35257372..35267692-chr6:35433856..35438688,25	K562	blood:
20	chr6:35270811..35278072-chr6:35434777..35439344,8	MCF-7	breast:
21	chr6:34855314..34856910-chr6:35435686..35437650,2	MCF-7	breast:
22	chr6:35309215..35314259-chr6:35432456..35439068,10	MCF-7	breast:
23	chr6:35435616..35437664-chrX:153627963..153630833,2	K562	blood:
24	chr6:35435945..35437939-chr6:35694170..35698146,4	MCF-7	breast:
25	chr16:75498144..75498858-chr6:35436601..35437554,2	HCT-116	colon:
26	chr6:35434775..35437842-chr6:35701549..35705876,5	MCF-7	breast:
27	chr6:35360426..35363519-chr6:35436261..35438354,3	K562	blood:
28	chr6:35415017..35416617-chr6:35436362..35437925,2	MCF-7	breast:
29	chr6:35415818..35424678-chr6:35432486..35440672,36	K562	blood:
30	chr6:35433822..35437754-chr6:35703135..35706478,6	K562	blood:
31	chr6:35260730..35269335-chr6:35433870..35444063,22	MCF-7	breast:
32	chr6:35434857..35438603-chr6:35692996..35696802,4	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-7111-3p	chr6:35438335-35438356	MIMAT0028120
hsa-miR-7111-5p	chr6:35438286-35438307	MIMAT0028119

No data

Variant related genes	Relation type
ENSG00000080546	chromatin interactions
ENSG00000064995	chromatin interactions
ENSG00000023892	chromatin interactions
ENSG00000112039	chromatin interactions
ENSG00000261717	chromatin interactions
ENSG00000147403	chromatin interactions
ENSG00000096060	chromatin interactions
ENSG00000232909	chromatin interactions
ENSG00000065029	chromatin interactions
ENSG00000123388	chromatin interactions
ENSG00000238184	chromatin interactions
ENSG00000196532	chromatin interactions
ENSG00000157343	chromatin interactions
ENSG00000112033	chromatin interactions
ENSG00000096063	chromatin interactions
ENSG00000110651	chromatin interactions
ENSG00000204140	chromatin interactions
ENSG00000183137	chromatin interactions
ENSG00000207165	chromatin interactions
ENSG00000166822	chromatin interactions

Extended variants
information (count: 55 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:55 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556586628	chr6:35437490-35437491	Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
2	rs184410434	chr6:35437553-35437554	Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
3	rs569332798	chr6:35437559-35437560	Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
4	rs143927052	chr6:35437561-35437562	Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
5	rs531978741	chr6:35437623-35437624	Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
6	rs551649451	chr6:35437628-35437629	Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
7	rs73415611	chr6:35437630-35437631	Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	16 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs542939270	chr6:35437635-35437636	Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
9	rs73415612	chr6:35437650-35437651	Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	14 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs371692150	chr6:35437687-35437688	Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
11	rs115419624	chr6:35437738-35437739	Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
12	rs562838136	chr6:35437747-35437748	Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
13	rs373466737	chr6:35437823-35437824	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
14	rs570291553	chr6:35437824-35437825	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
15	rs142495436	chr6:35437831-35437832	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
16	rs574664142	chr6:35437832-35437833	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
17	rs189046203	chr6:35437907-35437908	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs368854218	chr6:35437909-35437910	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs373502956	chr6:35437938-35437939	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs566943394	chr6:35437946-35437947	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs376367570	chr6:35437949-35437950	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs527929227	chr6:35437951-35437952	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs150793370	chr6:35437960-35437961	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs200246129	chr6:35437968-35437969	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs199735824	chr6:35437972-35437973	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs11553982	chr6:35437999-35438000	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs61734574	chr6:35438026-35438027	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs139332072	chr6:35438078-35438079	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs17838763	chr6:35438105-35438106	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs201025796	chr6:35438146-35438147	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs576596572	chr6:35438205-35438206	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs368296406	chr6:35438206-35438207	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs537818936	chr6:35438276-35438277	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs556262228	chr6:35438281-35438282	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs146033185	chr6:35438316-35438317	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs139957434	chr6:35438317-35438318	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs199597967	chr6:35438335-35438336	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region miRNA	6 gene(s)	Overlapped CNVs	n/a
38	rs181476065	chr6:35438347-35438348	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region miRNA	6 gene(s)	Overlapped CNVs	n/a
39	rs187631484	chr6:35438350-35438351	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region miRNA	6 gene(s)	Overlapped CNVs	n/a
40	rs144096254	chr6:35438386-35438387	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs146589879	chr6:35438387-35438388	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs1061530	chr6:35438392-35438393	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs554872305	chr6:35438404-35438405	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs11553976	chr6:35438405-35438406	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs111336248	chr6:35438419-35438420	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs4919	chr6:35438468-35438469	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs373864914	chr6:35438477-35438478	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs543731417	chr6:35438509-35438510	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs112121986	chr6:35438544-35438545	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs576813635	chr6:35438556-35438557	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Strong transcription Enhancers	Chromatin interactive region	6 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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:35435200-35440200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr6:35435600-35437600	Active TSS	Aorta	Aorta
3	chr6:35435600-35437600	Active TSS	Gastric	stomach
4	chr6:35435600-35437600	Active TSS	Sigmoid Colon	Sigmoid Colon
5	chr6:35435600-35437600	Active TSS	HSMMtube	muscle
6	chr6:35435600-35437600	Active TSS	NHDF-Ad	bronchial
7	chr6:35435600-35437800	Active TSS	Pancreatic Islets	Pancreatic Islet
8	chr6:35435600-35437800	Active TSS	Ovary	ovary
9	chr6:35435600-35437800	Active TSS	Small Intestine	intestine
10	chr6:35435600-35438800	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr6:35435800-35437600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr6:35435800-35437600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr6:35435800-35437600	Active TSS	Fetal Heart	heart
14	chr6:35435800-35437600	Active TSS	Placenta Amnion	Placenta Amnion
15	chr6:35435800-35437800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
16	chr6:35435800-35439200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr6:35435800-35439200	Transcr. at gene 5' and 3'	NHLF	lung
18	chr6:35436200-35438000	Transcr. at gene 5' and 3'	Primary T helper naive cells fromperipheralblood	blood
19	chr6:35436200-35438400	Transcr. at gene 5' and 3'	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr6:35436200-35438400	Transcr. at gene 5' and 3'	Primary T regulatory cells fromperipheralblood	blood
21	chr6:35436200-35440400	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
22	chr6:35436200-35440600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr6:35436400-35437800	Transcr. at gene 5' and 3'	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr6:35436400-35438400	Transcr. at gene 5' and 3'	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr6:35436400-35439200	Transcr. at gene 5' and 3'	HUES6 Cell Line	embryonic stem cell
26	chr6:35436400-35439200	Transcr. at gene 5' and 3'	A549	lung
27	chr6:35436400-35439200	Transcr. at gene 5' and 3'	Dnd41	blood
28	chr6:35436400-35439200	Transcr. at gene 5' and 3'	Osteobl	bone
29	chr6:35436400-35439400	Transcr. at gene 5' and 3'	iPS-15b Cell Line	embryonic stem cell
30	chr6:35436400-35439400	Transcr. at gene 5' and 3'	iPS-20b Cell Line	embryonic stem cell
31	chr6:35436400-35439400	Transcr. at gene 5' and 3'	Muscle Satellite Cultured Cells	--
32	chr6:35436400-35440200	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr6:35436400-35440200	Transcr. at gene 5' and 3'	NHEK	skin
34	chr6:35436400-35440600	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
35	chr6:35436600-35437600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
36	chr6:35436600-35437600	Active TSS	Right Atrium	heart
37	chr6:35436600-35437800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
38	chr6:35436600-35438000	Transcr. at gene 5' and 3'	Primary T cells fromperipheralblood	blood
39	chr6:35436600-35438000	Transcr. at gene 5' and 3'	Fetal Stomach	stomach
40	chr6:35436600-35438000	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
41	chr6:35436600-35438200	Transcr. at gene 5' and 3'	Fetal Muscle Leg	muscle
42	chr6:35436600-35438400	Transcr. at gene 5' and 3'	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr6:35436600-35438400	Flanking Active TSS	Primary hematopoietic stem cells	blood
44	chr6:35436600-35438400	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
45	chr6:35436600-35438800	Transcr. at gene 5' and 3'	ES-I3 Cell Line	embryonic stem cell
46	chr6:35436600-35438800	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr6:35436600-35438800	Transcr. at gene 5' and 3'	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr6:35436600-35438800	Transcr. at gene 5' and 3'	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr6:35436600-35439200	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
50	chr6:35436600-35439200	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin03	Skin

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