Variant report

Variant	nsv971680
Chromosome Location	chr8:87494100-87495999
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:95)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:95 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr8:87495577-87495766	A549	lung:	n/a	n/a
2	CTCF	chr8:87494809-87495128	K562	blood:	n/a	n/a
3	CTCF	chr8:87494960-87495110	A549	lung:	n/a	n/a
4	CTCF	chr8:87494940-87495090	GM12872	blood:	n/a	n/a
5	CTCF	chr8:87494900-87495050	MCF-7	breast:	n/a	n/a
6	CTCF	chr8:87495020-87495170	HCT-116	colon:	n/a	n/a
7	CTCF	chr8:87494900-87495050	A549	lung:	n/a	n/a
8	CTCF	chr8:87494915-87495043	NHEK	skin:	n/a	n/a
9	CTCF	chr8:87494940-87495090	WERI-Rb-1	eye:	n/a	n/a
10	CTCF	chr8:87494847-87495059	A549	lung:	n/a	n/a
11	CTCF	chr8:87494862-87495091	MCF-7	breast:	n/a	n/a
12	CTCF	chr8:87494840-87494990	HBMEC	blood vessel:	n/a	n/a
13	CTCF	chr8:87494844-87495105	MCF-7	breast:	n/a	n/a
14	CTCF	chr8:87494880-87495030	HMF	breast:	n/a	n/a
15	CTCF	chr8:87494880-87495030	HPAF	blood vessel:	n/a	n/a
16	CTCF	chr8:87494880-87495030	WERI-Rb-1	eye:	n/a	n/a
17	CTCF	chr8:87494889-87495042	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr8:87494841-87495101	MCF-7	breast:	n/a	n/a
19	CTCF	chr8:87495140-87495290	HCT-116	colon:	n/a	n/a
20	CTCF	chr8:87494920-87495070	AG09319	gingival:	n/a	n/a
21	CTCF	chr8:87494913-87495047	ProgFib	skin:	n/a	n/a
22	CTCF	chr8:87494920-87495070	GM12875	blood:	n/a	n/a
23	CTCF	chr8:87494900-87495050	GM12878	blood:	n/a	n/a
24	CTCF	chr8:87494900-87495050	Caco-2	colon:	n/a	n/a
25	CTCF	chr8:87494860-87495010	AG04449	skin:	n/a	n/a
26	CTCF	chr8:87494754-87495095	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr8:87494824-87495143	MCF-7	breast:	n/a	n/a
28	CTCF	chr8:87494860-87495010	GM12875	blood:	n/a	n/a
29	CTCF	chr8:87494900-87495050	GM12873	blood:	n/a	n/a
30	CTCF	chr8:87494858-87495053	GM12878	blood:	n/a	n/a
31	CTCF	chr8:87494920-87495070	GM12873	blood:	n/a	n/a
32	CTCF	chr8:87495020-87495170	BE2_C	brain:	n/a	n/a
33	CTCF	chr8:87494860-87495010	GM12878	blood:	n/a	n/a
34	CTCF	chr8:87494901-87495045	GM19240	blood:	n/a	n/a
35	CTCF	chr8:87494920-87495070	RPTEC	kidney:	n/a	n/a
36	CTCF	chr8:87494900-87495050	K562	blood:	n/a	n/a
37	CTCF	chr8:87494961-87494989	LNCaP	prostate:	n/a	n/a
38	CTCF	chr8:87494845-87495101	MCF-7	breast:	n/a	n/a
39	CTCF	chr8:87494860-87495010	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr8:87494787-87495155	GM12878	blood:	n/a	n/a
41	CTCF	chr8:87494880-87495030	GM06990	blood:	n/a	n/a
42	CTCF	chr8:87494825-87495166	K562	blood:	n/a	n/a
43	CTCF	chr8:87494855-87495092	MCF-7	breast:	n/a	n/a
44	CTCF	chr8:87494900-87495050	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr8:87494860-87495103	A549	lung:	n/a	n/a
46	CTCF	chr8:87494720-87494870	GM12872	blood:	n/a	n/a
47	CTCF	chr8:87494860-87495010	HCT-116	colon:	n/a	n/a
48	CTCF	chr8:87494840-87494990	HEK293	kidney:	n/a	n/a
49	CTCF	chr8:87494923-87495018	Fibrobl	skin:	n/a	n/a
50	CTCF	chr8:87494840-87494990	MCF-7	breast:	n/a	n/a

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:87489077..87491109-chr8:87492841..87495174,2	K562	blood:
2	chr8:87493659..87498581-chr8:87498622..87502865,4	MCF-7	breast:
3	chr8:87492324..87497991-chr8:87518822..87522169,6	MCF-7	breast:
4	chr8:87485122..87487844-chr8:87492423..87496426,3	K562	blood:
5	chr8:87488822..87490352-chr8:87494282..87496966,2	MCF-7	breast:
6	chr8:87495268..87498918-chr8:87499043..87502704,4	MCF-7	breast:
7	chr8:87485122..87487752-chr8:87491882..87495380,3	K562	blood:
8	chr8:87495583..87497504-chr8:87520238..87522113,2	K562	blood:

No data

Variant related genes	Relation type
RMDN1	TF binding region
CPNE3	TF binding region
NTAN1P2	TF binding region
ENSG00000176623	chromatin interactions

Extended variants
information (count: 76 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:76 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13257414	chr8:87494138-87494139	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs536904547	chr8:87494152-87494153	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs551853753	chr8:87494166-87494167	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs188391561	chr8:87494186-87494187	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs538792901	chr8:87494210-87494211	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs148369785	chr8:87494262-87494263	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs368295249	chr8:87494300-87494301	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs73273156	chr8:87494302-87494303	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs564236223	chr8:87494305-87494306	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs34799067	chr8:87494319-87494320	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs532585005	chr8:87494327-87494328	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs554959350	chr8:87494448-87494449	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs574784544	chr8:87494456-87494457	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs547988590	chr8:87494528-87494529	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs181015024	chr8:87494558-87494559	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs560104541	chr8:87494579-87494580	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs145778770	chr8:87494604-87494605	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs566216900	chr8:87494621-87494622	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs545608216	chr8:87494655-87494656	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs138437273	chr8:87494671-87494672	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs531265952	chr8:87494693-87494694	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs548561047	chr8:87494694-87494695	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs375229945	chr8:87494737-87494738	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs570053830	chr8:87494740-87494741	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs561319384	chr8:87494746-87494747	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs372498848	chr8:87494747-87494748	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs377570493	chr8:87494748-87494749	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs530346274	chr8:87494753-87494754	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs537136803	chr8:87494754-87494755	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs111857927	chr8:87494795-87494796	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs566983543	chr8:87494809-87494810	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs146103549	chr8:87494838-87494839	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs375987968	chr8:87494865-87494866	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs552743955	chr8:87494866-87494867	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs569381157	chr8:87494886-87494887	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs538293417	chr8:87494892-87494893	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs555022071	chr8:87494893-87494894	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs574741206	chr8:87494899-87494900	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs534631552	chr8:87494903-87494904	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs537487189	chr8:87494908-87494909	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs554010992	chr8:87494911-87494912	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs559069387	chr8:87494943-87494944	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs185038986	chr8:87494944-87494945	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs4961194	chr8:87494974-87494975	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs34980071	chr8:87495055-87495056	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs562297486	chr8:87495099-87495100	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs373267435	chr8:87495112-87495113	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs575755267	chr8:87495160-87495161	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs541490322	chr8:87495165-87495166	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs561384007	chr8:87495184-87495185	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:116)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Autism	20841430	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Colorectal cancer	21645411	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:218 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:87441800-87507600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr8:87448800-87502800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr8:87457400-87507400	Weak transcription	Brain Angular Gyrus	brain
4	chr8:87459200-87499600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr8:87461000-87494200	Weak transcription	Brain Substantia Nigra	brain
6	chr8:87471000-87497800	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr8:87473800-87494200	Weak transcription	Brain Hippocampus Middle	brain
8	chr8:87474000-87517000	Weak transcription	Small Intestine	intestine
9	chr8:87477400-87494200	Weak transcription	Rectal Smooth Muscle	rectum
10	chr8:87477800-87494200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr8:87477800-87494600	Weak transcription	Aorta	Aorta
12	chr8:87478000-87494200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr8:87479600-87499400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr8:87481400-87494200	Weak transcription	Right Ventricle	heart
15	chr8:87481800-87494200	Weak transcription	Gastric	stomach
16	chr8:87481800-87494800	Weak transcription	Spleen	Spleen
17	chr8:87481800-87507400	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr8:87481800-87507600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr8:87481800-87507600	Weak transcription	Esophagus	oesophagus
20	chr8:87482000-87494200	Weak transcription	Thymus	Thymus
21	chr8:87482000-87496400	Weak transcription	Brain Anterior Caudate	brain
22	chr8:87482000-87507600	Weak transcription	Fetal Brain Male	brain
23	chr8:87482000-87508200	Weak transcription	Fetal Heart	heart
24	chr8:87482000-87508400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr8:87482200-87494200	Weak transcription	Brain Cingulate Gyrus	brain
26	chr8:87482200-87495800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr8:87482200-87496400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr8:87482200-87507600	Weak transcription	Colonic Mucosa	Colon
29	chr8:87482400-87517000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr8:87482600-87494200	Weak transcription	K562	blood
31	chr8:87482600-87494800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr8:87482600-87494800	Weak transcription	Lung	lung
33	chr8:87482800-87494200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr8:87482800-87494200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr8:87482800-87494200	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr8:87482800-87496400	Weak transcription	Brain Germinal Matrix	brain
37	chr8:87482800-87503400	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr8:87482800-87506600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr8:87482800-87519600	Weak transcription	HUVEC	blood vessel
40	chr8:87483000-87494200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr8:87483000-87508400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr8:87483200-87494200	Weak transcription	Ovary	ovary
43	chr8:87483200-87505400	Weak transcription	Hela-S3	cervix
44	chr8:87483400-87494800	Weak transcription	Fetal Brain Female	brain
45	chr8:87484400-87494800	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr8:87484600-87494200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
47	chr8:87484800-87494800	Weak transcription	Left Ventricle	heart
48	chr8:87485000-87501200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
49	chr8:87485400-87494200	Weak transcription	Rectal Mucosa Donor 29	rectum
50	chr8:87486000-87494800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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