Variant report

Variant	nsv510709
Chromosome Location	chr17:37438419-37508395
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:309)
CpG islands
(count:0)
Chromatin interactive
region (count:42)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:309 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:37478340-37478368	K562	blood:	n/a	n/a
2	ARID3A	chr17:37478587-37478766	K562	blood:	n/a	n/a
3	ARID3A	chr17:37490816-37491597	K562	blood:	n/a	n/a
4	ARID3A	chr17:37492392-37492411	K562	blood:	n/a	n/a
5	ATF1	chr17:37482135-37482477	K562	blood:	n/a	n/a
6	ATF1	chr17:37457990-37458253	K562	blood:	n/a	n/a
7	ATF1	chr17:37490885-37491566	K562	blood:	n/a	n/a
8	ATF2	chr17:37462736-37463171	GM12878	blood:	n/a	n/a
9	ATF3	chr17:37491217-37491638	K562	blood:	n/a	n/a
10	ATF3	chr17:37490868-37491124	K562	blood:	n/a	n/a
11	ATF3	chr17:37477551-37477852	K562	blood:	n/a	n/a
12	ATF3	chr17:37457998-37458261	K562	blood:	n/a	n/a
13	BHLHE40	chr17:37491295-37492343	K562	blood:	n/a	n/a
14	BHLHE40	chr17:37490999-37491075	K562	blood:	n/a	n/a
15	BHLHE40	chr17:37457701-37458316	K562	blood:	n/a	n/a
16	CBX3	chr17:37491118-37491653	K562	blood:	n/a	n/a
17	CBX3	chr17:37457873-37458230	K562	blood:	n/a	n/a
18	CCNT2	chr17:37457971-37458185	K562	blood:	n/a	n/a
19	CCNT2	chr17:37482228-37482393	K562	blood:	n/a	n/a
20	CCNT2	chr17:37490996-37491490	K562	blood:	n/a	n/a
21	CEBPB	chr17:37477481-37477835	K562	blood:	n/a	n/a
22	CEBPB	chr17:37479002-37479151	K562	blood:	n/a	n/a
23	CEBPB	chr17:37499007-37499179	K562	blood:	n/a	n/a
24	CEBPB	chr17:37481864-37482186	K562	blood:	n/a	n/a
25	CEBPB	chr17:37439326-37439688	K562	blood:	n/a	n/a
26	CEBPB	chr17:37440307-37440433	A549	lung:	n/a	chr17:37440380-37440391
27	CEBPB	chr17:37491309-37491559	K562	blood:	n/a	n/a
28	CEBPB	chr17:37480901-37481059	HepG2	liver:	n/a	chr17:37480909-37480920 chr17:37480981-37480994 chr17:37480982-37480993 chr17:37480908-37480925
29	CEBPB	chr17:37491280-37491603	K562	blood:	n/a	n/a
30	CEBPB	chr17:37439436-37439675	MCF-7	breast:	n/a	n/a
31	CEBPB	chr17:37439351-37439714	MCF-7	breast:	n/a	n/a
32	CEBPB	chr17:37440293-37440538	HepG2	liver:	n/a	chr17:37440380-37440391
33	CEBPB	chr17:37491087-37491660	K562	blood:	n/a	n/a
34	CEBPB	chr17:37477546-37477814	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr17:37470168-37470397	K562	blood:	n/a	n/a
36	CEBPB	chr17:37505056-37505192	HepG2	liver:	n/a	chr17:37505148-37505159
37	CEBPB	chr17:37442395-37442613	K562	blood:	n/a	n/a
38	CEBPB	chr17:37491992-37492192	K562	blood:	n/a	n/a
39	CEBPB	chr17:37470144-37470379	IMR90	lung:	n/a	n/a
40	CEBPB	chr17:37477549-37477821	K562	blood:	n/a	n/a
41	CEBPB	chr17:37490421-37491059	K562	blood:	n/a	n/a
42	CEBPD	chr17:37490855-37491669	K562	blood:	n/a	n/a
43	CTCF	chr17:37447751-37447825	GM20000	blood:	n/a	n/a
44	CTCF	chr17:37500385-37500508	Lung_OC	lung:	n/a	n/a
45	CTCF	chr17:37497860-37498010	GM12872	blood:	n/a	n/a
46	CTCF	chr17:37457923-37457945	Fibrobl	skin:	n/a	n/a
47	CTCF	chr17:37447057-37447106	GM20000	blood:	n/a	n/a
48	CTCF	chr17:37504860-37505010	GM12864	blood:	n/a	n/a
49	CTCF	chr17:37468899-37468946	Fibrobl	skin:	n/a	n/a
50	CTCF	chr17:37474189-37474267	GM10248	blood:	n/a	n/a

No data

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:37464074..37466279-chr17:37474396..37477134,2	K562	blood:
2	chr17:37445187..37446849-chr17:37448541..37450328,2	K562	blood:
3	chr17:37447109..37449563-chr17:37453918..37456392,2	K562	blood:
4	chr17:37440390..37443077-chr17:37445532..37447421,2	K562	blood:
5	chr17:37507661..37509338-chr17:37520135..37522515,3	K562	blood:
6	chr17:37496486..37499725-chr17:37507468..37510514,3	K562	blood:
7	chr17:37495025..37499725-chr17:37506231..37509469,4	K562	blood:
8	chr17:37483771..37485642-chr17:37488722..37490258,2	K562	blood:
9	chr17:37508217..37510563-chr17:37511063..37514093,3	K562	blood:
10	chr17:37497042..37498791-chr17:37515042..37516791,2	K562	blood:
11	chr17:37479901..37481702-chr17:37484726..37486933,2	K562	blood:
12	chr17:37355091..37357446-chr17:37477278..37479743,2	K562	blood:
13	chr17:37479901..37481702-chr17:37484726..37486933,2	K562	blood:
14	chr17:37454099..37457029-chr17:37517737..37519979,2	K562	blood:
15	chr17:37493150..37495079-chr17:37497859..37499627,2	K562	blood:
16	chr17:37459079..37461538-chr17:37464843..37466379,2	MCF-7	breast:
17	chr17:37492064..37493936-chr17:37496192..37498090,2	K562	blood:
18	chr17:37464074..37466279-chr17:37474396..37477134,2	K562	blood:
19	chr17:37493150..37495079-chr17:37497859..37499627,2	K562	blood:
20	chr17:37463799..37466279-chr17:37472914..37477134,3	K562	blood:
21	chr17:37478446..37480205-chr17:37480429..37483200,2	K562	blood:
22	chr17:37441688..37444603-chr17:37616423..37619369,2	K562	blood:
23	chr17:37495025..37499725-chr17:37506231..37509469,4	K562	blood:
24	chr17:37471557..37473905-chr17:37476618..37478762,2	K562	blood:
25	chr17:37492064..37493936-chr17:37496192..37498090,2	K562	blood:
26	chr17:37478446..37480205-chr17:37480429..37483200,2	K562	blood:
27	chr17:37496486..37499725-chr17:37507468..37510514,3	K562	blood:
28	chr17:37445187..37446849-chr17:37448541..37450328,2	K562	blood:
29	chr17:37440390..37443077-chr17:37445532..37447421,2	K562	blood:
30	chr17:37358593..37361513-chr17:37484361..37486028,2	K562	blood:
31	chr17:37483771..37485642-chr17:37488722..37490258,2	K562	blood:
32	chr17:37507828..37510744-chr17:37514952..37516459,2	K562	blood:
33	chr17:37463799..37466279-chr17:37472914..37477134,3	K562	blood:
34	chr17:37507720..37510476-chr17:37512296..37514267,2	MCF-7	breast:
35	chr17:37471557..37473905-chr17:37476618..37478762,2	K562	blood:
36	chr17:37497908..37499524-chr17:37499722..37502631,3	K562	blood:
37	chr17:37488107..37492015-chr17:37616604..37619241,3	K562	blood:
38	chr17:37497908..37499524-chr17:37499722..37502631,3	K562	blood:
39	chr17:37459079..37461538-chr17:37464843..37466379,2	MCF-7	breast:
40	chr17:37447109..37449563-chr17:37453918..37456392,2	K562	blood:
41	chr17:37444148..37446120-chr17:37795463..37797673,2	K562	blood:
42	chr17:37442218..37445626-chr17:37557595..37560949,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000265904	TF binding region
ENSG00000108306	chromatin interactions
ENSG00000167258	chromatin interactions
ENSG00000108298	chromatin interactions
ENSG00000266469	chromatin interactions

Extended variants
information (count: 2809 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:2809 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566065792	chr17:37438435-37438436	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs151224029	chr17:37438485-37438486	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs575287920	chr17:37438539-37438540	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs554962994	chr17:37438549-37438550	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs575999004	chr17:37438574-37438575	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs566883798	chr17:37438577-37438578	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs140387004	chr17:37438597-37438598	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs556033219	chr17:37438606-37438607	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577645589	chr17:37438682-37438683	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs543396302	chr17:37438697-37438698	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs185354767	chr17:37438772-37438773	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs116522643	chr17:37438780-37438781	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs369059774	chr17:37438931-37438932	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs375330118	chr17:37438932-37438933	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs376772607	chr17:37438942-37438943	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs190064587	chr17:37438943-37438944	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs150361719	chr17:37438951-37438952	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs368889265	chr17:37438952-37438953	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs182755000	chr17:37438960-37438961	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs186839014	chr17:37438969-37438970	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs138100680	chr17:37438972-37438973	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs532621624	chr17:37438986-37438987	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs112732101	chr17:37439013-37439014	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs57598101	chr17:37439014-37439015	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs141150945	chr17:37439042-37439043	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs143474058	chr17:37439081-37439082	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs73308830	chr17:37439124-37439125	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs374470184	chr17:37439129-37439130	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs75637050	chr17:37439133-37439134	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs377503075	chr17:37439139-37439140	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs548512124	chr17:37439168-37439169	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs570327040	chr17:37439181-37439182	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs537471448	chr17:37439205-37439206	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs199955059	chr17:37439212-37439213	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs560930026	chr17:37439251-37439252	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369845643	chr17:37439264-37439265	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs373044456	chr17:37439286-37439287	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571273834	chr17:37439321-37439322	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs538711350	chr17:37439330-37439331	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs118138584	chr17:37439380-37439381	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs112711854	chr17:37439399-37439400	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs191527282	chr17:37439408-37439409	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs536439570	chr17:37439419-37439420	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs142137318	chr17:37439462-37439463	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs370307329	chr17:37439468-37439469	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs554947017	chr17:37439479-37439480	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs183791095	chr17:37439490-37439491	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs602688	chr17:37439496-37439497	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs565248789	chr17:37439497-37439498	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs111722736	chr17:37439531-37439532	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17157792	CNVD
Bladder cancer	19088036	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Meningioma	19431122	CNVD
Neurocytoma	17123091	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	24379144	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	17850661	CNVD
Primary lung adenocarcinoma	16799635	CNVD
HIV/AIDS	18848619	CNVD
Rheumatoid arthritis	19220326	CNVD
Rheumatoid arthritis	18848619	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	18848619	CNVD
Type 1 diabetes	19220326	CNVD
HIV/AIDS	17330138	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	19955444	CNVD
Schizophrenia	19955444	CNVD
Acute monocytic leukemia	16498392	CNVD
Breast cancer	20409316	CNVD
Myelodysplastic syndrome	18663149	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Sezary syndrome	18413736	CNVD
Cancer	20164920	CNVD
Cancer	17440070	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1089 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:37407200-37439200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr17:37408000-37440200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr17:37408000-37441600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr17:37408000-37463000	Weak transcription	Small Intestine	intestine
5	chr17:37408200-37442400	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr17:37409000-37438800	Strong transcription	Primary neutrophils fromperipheralblood	blood
7	chr17:37409800-37464000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr17:37415000-37443600	Weak transcription	Psoas Muscle	Psoas
9	chr17:37417400-37458600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr17:37417600-37460800	Weak transcription	Fetal Brain Male	brain
11	chr17:37418400-37440800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr17:37425000-37473000	Weak transcription	Pancreas	Pancrea
13	chr17:37426200-37453800	Weak transcription	Aorta	Aorta
14	chr17:37426600-37460800	Weak transcription	Colonic Mucosa	Colon
15	chr17:37426800-37468600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr17:37429200-37439400	Strong transcription	Primary monocytes fromperipheralblood	blood
17	chr17:37430800-37462600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr17:37431000-37443600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr17:37431200-37450800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr17:37431200-37453200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr17:37431200-37453200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr17:37431200-37453200	Weak transcription	Rectal Smooth Muscle	rectum
23	chr17:37431200-37462600	Weak transcription	Colon Smooth Muscle	Colon
24	chr17:37431400-37438600	Weak transcription	Primary hematopoietic stem cells	blood
25	chr17:37431400-37443600	Weak transcription	Left Ventricle	heart
26	chr17:37431400-37452800	Weak transcription	Dnd41	blood
27	chr17:37431400-37453000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr17:37431400-37453200	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr17:37431400-37453200	Weak transcription	Brain Substantia Nigra	brain
30	chr17:37431400-37453600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
31	chr17:37431400-37453600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr17:37431400-37473400	Weak transcription	Esophagus	oesophagus
33	chr17:37431600-37442000	Weak transcription	Brain Germinal Matrix	brain
34	chr17:37431600-37453000	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr17:37431600-37453800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr17:37431600-37453800	Weak transcription	Right Ventricle	heart
37	chr17:37433000-37439200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr17:37433000-37439400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr17:37433000-37441600	Strong transcription	Primary T helper cells fromperipheralblood	blood
40	chr17:37433400-37444400	Strong transcription	Fetal Thymus	thymus
41	chr17:37433600-37441200	Strong transcription	Primary T cells fromperipheralblood	blood
42	chr17:37433800-37457000	Weak transcription	GM12878-XiMat	blood
43	chr17:37434000-37442400	Strong transcription	Primary T cells from cord blood	blood
44	chr17:37434000-37452400	Weak transcription	Primary B cells from peripheral blood	blood
45	chr17:37434200-37453200	Weak transcription	Primary B cells from cord blood	blood
46	chr17:37434400-37441600	Strong transcription	Thymus	Thymus
47	chr17:37434800-37450200	Weak transcription	Lung	lung
48	chr17:37435200-37453400	Weak transcription	Brain Cingulate Gyrus	brain
49	chr17:37435600-37469400	Weak transcription	Gastric	stomach
50	chr17:37435800-37440800	Weak transcription	Brain Angular Gyrus	brain

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