Variant report

Variant	nsv823502
Chromosome Location	chr6:31777657-31779623
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:21)
CpG islands
(count:1834)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:21 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	EBF1	chr6:31779535-31779720	GM12878	blood:	n/a	n/a
2	EGR1	chr6:31778327-31778581	K562	blood:	n/a	n/a
3	ESR1	chr6:31778208-31778582	ECC-1	luminal epithelium:	n/a	chr6:31778361-31778376
4	HEY1	chr6:31779455-31779732	K562	blood:	n/a	n/a
5	HEY1	chr6:31778811-31779030	K562	blood:	n/a	n/a
6	MYC	chr6:31778537-31778540	MCF-7	breast:	n/a	n/a
7	MYC	chr6:31778542-31778588	MCF-7	breast:	n/a	n/a
8	POLR2A	chr6:31779553-31779697	Hela-S3	cervix:	n/a	n/a
9	POLR2A	chr6:31778581-31778582	MCF-7	breast:	n/a	n/a
10	POLR2A	chr6:31779568-31779735	GM12878	blood:	n/a	n/a
11	POLR2A	chr6:31778593-31778600	MCF-7	breast:	n/a	n/a
12	POLR2A	chr6:31779526-31779719	GM12878	blood:	n/a	n/a
13	POLR2A	chr6:31779461-31779790	H1-hESC	embryonic stem cell:	n/a	n/a
14	POLR2A	chr6:31778519-31778541	MCF-7	breast:	n/a	n/a
15	POLR2A	chr6:31778582-31778591	MCF-7	breast:	n/a	n/a
16	POLR2A	chr6:31778507-31778518	MCF-7	breast:	n/a	n/a
17	POLR2A	chr6:31778550-31778568	MCF-7	breast:	n/a	n/a
18	POLR2A	chr6:31778853-31779030	GM12878	blood:	n/a	n/a
19	POLR2A	chr6:31778863-31779030	GM12878	blood:	n/a	n/a
20	POLR2A	chr6:31778532-31778544	MCF-7	breast:	n/a	n/a
21	SIN3AK20	chr6:31779530-31779699	HepG2	liver:	n/a	n/a

(count:1834 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31779529-31779579	ECC-1	luminal epithelium:	n/a
2	chr6:31779020-31779070	Jurkat	blood:	n/a
3	chr6:31778408-31778458	Jurkat	blood:	n/a
4	chr6:31778784-31778834	ovcar-3	ovarian:	n/a
5	chr6:31779529-31779579	ECC-1	luminal epithelium:	n/a
6	chr6:31779020-31779070	Jurkat	blood:	n/a
7	chr6:31778408-31778458	Jurkat	blood:	n/a
8	chr6:31778784-31778834	ovcar-3	ovarian:	n/a
9	chr6:31779529-31779579	AG09319	gingival:	n/a
10	chr6:31779529-31779579	SKMC	muscle:	n/a
11	chr6:31779381-31779431	AG04449	skin:	fetal
12	chr6:31778007-31778057	Jurkat	blood:	n/a
13	chr6:31778194-31778244	MCF10A-Er-Src	breast:	n/a
14	chr6:31778622-31778672	Hepatocyte	liver:	n/a
15	chr6:31777883-31777933	K562	blood:	n/a
16	chr6:31778674-31778724	BE2_C	brain:	n/a
17	chr6:31778007-31778057	ovcar-3	ovarian:	n/a
18	chr6:31778408-31778458	HMEC	breast:	n/a
19	chr6:31778784-31778834	GM06990	blood:	n/a
20	chr6:31779521-31779571	HEEpiC	esophagus:	n/a
21	chr6:31778639-31778689	HepG2	liver:	n/a
22	chr6:31779582-31779632	HCM	heart:	n/a
23	chr6:31778674-31778724	GM12892	blood:	n/a
24	chr6:31779020-31779070	K562	blood:	n/a
25	chr6:31779598-31779648	PANC-1	pancreas:	n/a
26	chr6:31778639-31778689	HRCEpiC	kidney:	n/a
27	chr6:31777609-31777659	ECC-1	luminal epithelium:	n/a
28	chr6:31778842-31778892	HRCEpiC	kidney:	n/a
29	chr6:31779308-31779358	PANC-1	pancreas:	n/a
30	chr6:31778622-31778672	HEK293	kidney:	embryo
31	chr6:31778701-31778751	GM06990	blood:	n/a
32	chr6:31778408-31778458	AG04449	skin:	fetal
33	chr6:31778519-31778569	AG09309	skin:	n/a
34	chr6:31778919-31778969	SKMC	muscle:	n/a
35	chr6:31778558-31778608	GM12878	blood:	n/a
36	chr6:31779529-31779579	SK-N-SH	brain:	n/a
37	chr6:31778701-31778751	HepG2	liver:	n/a
38	chr6:31778258-31778308	ovcar-3	ovarian:	n/a
39	chr6:31778519-31778569	HEEpiC	esophagus:	n/a
40	chr6:31778519-31778569	PANC-1	pancreas:	n/a
41	chr6:31778371-31778421	HCT-116	colon:	n/a
42	chr6:31779620-31779670	GM12892	blood:	n/a
43	chr6:31779620-31779670	BJ	skin:	n/a
44	chr6:31778639-31778689	Jurkat	blood:	n/a
45	chr6:31779582-31779632	HRCEpiC	kidney:	n/a
46	chr6:31778018-31778068	RPTEC	kidney:	n/a
47	chr6:31778558-31778608	SK-N-SH	brain:	n/a
48	chr6:31778258-31778308	HNPCEpiC	eye:	n/a
49	chr6:31778784-31778834	Caco-2	colon:	n/a
50	chr6:31778519-31778569	HCF	heart:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31707248..31709508-chr6:31776899..31779251,2	MCF-7	breast:
2	chr6:31779052..31779558-chr6:31795475..31796031,2	Hela-S3	cervix:
3	chr6:31762241..31764929-chr6:31776890..31779670,2	MCF-7	breast:
4	chr6:31778125..31780067-chr6:31938272..31940991,2	MCF-7	breast:
5	chr6:31702718..31704412-chr6:31776913..31779697,2	MCF-7	breast:

No data

Variant related genes	Relation type
LSM2	TF binding region
HSPA1A	TF binding region
LSM2	CpG island
HSPA1A	CpG island
ENSG00000255152	chromatin interactions
ENSG00000213719	chromatin interactions
ENSG00000204410	chromatin interactions
ENSG00000204394	chromatin interactions
ENSG00000204388	chromatin interactions
ENSG00000204344	chromatin interactions
ENSG00000204348	chromatin interactions

Extended variants
information (count: 109 )
Associated
traits (count: 131 )

Variant overlapped rSNPs/rCNVs (count:109 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371621895	chr6:31777774-31777775	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs576949512	chr6:31777822-31777823	Weak transcription Strong transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs150873641	chr6:31777832-31777833	Weak transcription Strong transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs370564561	chr6:31777841-31777842	Weak transcription Strong transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs202159508	chr6:31777859-31777860	Weak transcription Strong transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs550139982	chr6:31777887-31777888	Weak transcription Strong transcription Active TSS	CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs377450492	chr6:31777907-31777908	Weak transcription Strong transcription Active TSS	CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs371226757	chr6:31777936-31777937	Weak transcription Strong transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs2075800	chr6:31777946-31777947	Weak transcription Strong transcription Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs201332987	chr6:31777957-31777958	Weak transcription Strong transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs61751215	chr6:31777971-31777972	Weak transcription Strong transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs202033031	chr6:31777976-31777977	Weak transcription Strong transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs144451142	chr6:31777993-31777994	Weak transcription Strong transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs371717441	chr6:31778008-31778009	Weak transcription Strong transcription Active TSS	CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs554479408	chr6:31778016-31778017	Weak transcription Strong transcription Active TSS	CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs139052456	chr6:31778018-31778019	Weak transcription Strong transcription Active TSS	CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs567637853	chr6:31778041-31778042	Weak transcription Strong transcription Active TSS	CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs199974706	chr6:31778053-31778054	Weak transcription Strong transcription Active TSS	CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs566393477	chr6:31778076-31778077	Weak transcription Strong transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs2227955	chr6:31778077-31778078	Weak transcription Strong transcription Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs111462391	chr6:31778101-31778102	Weak transcription Strong transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs146402090	chr6:31778107-31778108	Weak transcription Strong transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs146531367	chr6:31778110-31778111	Weak transcription Strong transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs554869938	chr6:31778131-31778132	Weak transcription Strong transcription Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs201132627	chr6:31778144-31778145	Weak transcription Strong transcription Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs544006150	chr6:31778179-31778180	Weak transcription Strong transcription Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs139969031	chr6:31778195-31778196	Weak transcription Strong transcription Active TSS	CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs148694457	chr6:31778219-31778220	Weak transcription Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs200301187	chr6:31778237-31778238	Weak transcription Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs576268420	chr6:31778266-31778267	Weak transcription Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs2227956	chr6:31778272-31778273	Weak transcription Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs527582506	chr6:31778277-31778278	Weak transcription Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs548364201	chr6:31778299-31778300	Weak transcription Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs532485515	chr6:31778313-31778314	Weak transcription Strong transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs147667814	chr6:31778371-31778372	Weak transcription Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs200372086	chr6:31778376-31778377	Weak transcription Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs201161706	chr6:31778432-31778433	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs571792102	chr6:31778435-31778436	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs199726010	chr6:31778436-31778437	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs367836600	chr6:31778458-31778459	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs17853299	chr6:31778507-31778508	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs2075799	chr6:31778529-31778530	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
43	rs566332175	chr6:31778530-31778531	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs372714721	chr6:31778539-31778540	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs146348020	chr6:31778544-31778545	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs555125949	chr6:31778554-31778555	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs139384991	chr6:31778558-31778559	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs149424950	chr6:31778559-31778560	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs143774785	chr6:31778580-31778581	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs141209981	chr6:31778587-31778588	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:131)

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
Lung cancer	18438408	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
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ovarian cancer	21781307	CNVD
Ependymoma	19289631	CNVD
Breast cancer	22844521	CNVD
Gestational infection	22844521	CNVD
HIV/AIDS	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	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
Renal cell carcinoma	18765545	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
abnormal development	18461090	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	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
Breast cancer	21364760	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
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	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
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31774600-31780600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr6:31774600-31781400	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr6:31774600-31781600	Weak transcription	Aorta	Aorta
4	chr6:31774800-31778200	Weak transcription	Ovary	ovary
5	chr6:31774800-31780800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr6:31774800-31781000	Weak transcription	Psoas Muscle	Psoas
7	chr6:31774800-31781200	Weak transcription	Spleen	Spleen
8	chr6:31774800-31781400	Weak transcription	Brain Angular Gyrus	brain
9	chr6:31774800-31781400	Weak transcription	Brain Cingulate Gyrus	brain
10	chr6:31774800-31781400	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr6:31774800-31781800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr6:31774800-31781800	Weak transcription	Pancreas	Pancrea
13	chr6:31774800-31782600	Weak transcription	Lung	lung
14	chr6:31774800-31783000	Weak transcription	Gastric	stomach
15	chr6:31775000-31777800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr6:31775000-31777800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr6:31775000-31778400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr6:31775000-31780600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr6:31775000-31780600	Weak transcription	HMEC	breast
20	chr6:31775000-31781200	Weak transcription	HSMMtube	muscle
21	chr6:31775000-31781400	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr6:31775000-31781600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr6:31775000-31781600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr6:31775000-31781600	Weak transcription	Colonic Mucosa	Colon
25	chr6:31775000-31781600	Weak transcription	Right Atrium	heart
26	chr6:31775200-31777800	Weak transcription	Stomach Smooth Muscle	stomach
27	chr6:31775200-31778000	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr6:31775200-31778200	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr6:31775200-31779400	Weak transcription	GM12878-XiMat	blood
30	chr6:31775200-31780200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr6:31775200-31780600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr6:31775200-31781000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr6:31775200-31781000	Weak transcription	Fetal Muscle Trunk	muscle
34	chr6:31775200-31781000	Weak transcription	Stomach Mucosa	stomach
35	chr6:31775200-31781200	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr6:31775200-31781400	Weak transcription	Brain Anterior Caudate	brain
37	chr6:31775200-31781400	Weak transcription	Brain Substantia Nigra	brain
38	chr6:31775200-31781400	Weak transcription	Duodenum Mucosa	Duodenum
39	chr6:31775200-31781400	Weak transcription	Fetal Intestine Large	intestine
40	chr6:31775200-31781400	Weak transcription	Fetal Intestine Small	intestine
41	chr6:31775200-31781400	Weak transcription	Fetal Kidney	kidney
42	chr6:31775200-31781400	Weak transcription	Rectal Smooth Muscle	rectum
43	chr6:31775200-31781600	Weak transcription	Fetal Lung	lung
44	chr6:31775400-31777800	Weak transcription	Fetal Stomach	stomach
45	chr6:31775400-31778000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr6:31775400-31778400	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr6:31775400-31778800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr6:31775400-31780200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
49	chr6:31775400-31780400	Weak transcription	Primary B cells from cord blood	blood
50	chr6:31775400-31780600	Weak transcription	Skeletal Muscle Female	skeletal muscle

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