Variant report

Variant	nsv971330
Chromosome Location	chr8:86483944-86550441
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:186)
CpG islands
(count:122)
Chromatin interactive
region (count:11)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:186 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr8:86494789-86495026	K562	blood:	n/a	n/a
2	BHLHE40	chr8:86530061-86530136	K562	blood:	n/a	n/a
3	CEBPB	chr8:86526617-86526827	K562	blood:	n/a	chr8:86526677-86526688
4	CEBPB	chr8:86505964-86506372	MCF-7	breast:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
5	CEBPB	chr8:86541828-86542028	HepG2	liver:	n/a	chr8:86541944-86541955
6	CEBPB	chr8:86506011-86506339	MCF-7	breast:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
7	CEBPB	chr8:86506027-86506610	HepG2	liver:	n/a	chr8:86506202-86506211 chr8:86506581-86506598 chr8:86506488-86506500 chr8:86506200-86506211
8	CEBPB	chr8:86506026-86506381	A549	lung:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
9	CEBPB	chr8:86506021-86506349	H1-hESC	embryonic stem cell:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
10	CEBPB	chr8:86526496-86526857	IMR90	lung:	n/a	chr8:86526677-86526688
11	CEBPB	chr8:86526501-86526858	HepG2	liver:	n/a	chr8:86526677-86526688
12	CEBPB	chr8:86548074-86548266	HepG2	liver:	n/a	chr8:86548177-86548194
13	CEBPB	chr8:86506081-86506340	K562	blood:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
14	CEBPB	chr8:86526551-86526947	ECC-1	luminal epithelium:	n/a	chr8:86526677-86526688
15	CEBPB	chr8:86526519-86526866	A549	lung:	n/a	chr8:86526677-86526688
16	CEBPB	chr8:86526425-86526941	MCF-7	breast:	n/a	chr8:86526677-86526688
17	CEBPB	chr8:86506060-86506371	IMR90	lung:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
18	CEBPB	chr8:86526484-86526818	ECC-1	luminal epithelium:	n/a	chr8:86526677-86526688
19	CHD2	chr8:86509594-86509815	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr8:86488793-86488916	ProgFib	skin:	n/a	n/a
21	CTCF	chr8:86501940-86502090	HRE	kidney:	n/a	n/a
22	CTCF	chr8:86488825-86488916	GM12891	blood:	n/a	n/a
23	CTCF	chr8:86488840-86488915	GM19240	blood:	n/a	n/a
24	CTCF	chr8:86541400-86541550	HA-sp	spinal cord:	n/a	n/a
25	CTCF	chr8:86488799-86488917	MCF-7	breast:	n/a	n/a
26	CTCF	chr8:86488790-86488916	Fibrobl	skin:	n/a	n/a
27	CTCF	chr8:86515129-86515167	GM20000	blood:	n/a	n/a
28	CTCF	chr8:86488842-86488876	GM19238	blood:	n/a	n/a
29	CTCF	chr8:86488877-86488897	GM19238	blood:	n/a	n/a
30	CTCF	chr8:86488813-86488918	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr8:86500740-86500890	HCT-116	colon:	n/a	n/a
32	CTCF	chr8:86488826-86488917	MCF-7	breast:	n/a	n/a
33	CTCF	chr8:86488811-86488916	A549	lung:	n/a	n/a
34	CTCF	chr8:86488806-86488916	MCF-7	breast:	n/a	n/a
35	CTCF	chr8:86509421-86509521	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr8:86494371-86494488	GM12878	blood:	n/a	n/a
37	CTCF	chr8:86544750-86544836	Pancreas_OC	pancreas:	n/a	n/a
38	CTCF	chr8:86494374-86494479	GM19239	blood:	n/a	n/a
39	CTCF	chr8:86520432-86520511	Kidney_OC	kidney:	n/a	n/a
40	E2F4	chr8:86528535-86528749	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr8:86505700-86505895	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr8:86502777-86502819	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr8:86547943-86548263	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F6	chr8:86487592-86487938	H1-hESC	embryonic stem cell:	n/a	n/a
45	EBF1	chr8:86548212-86548420	GM12878	blood:	n/a	chr8:86548316-86548326
46	EP300	chr8:86488817-86488952	GM12878	blood:	n/a	n/a
47	EP300	chr8:86530109-86530133	K562	blood:	n/a	n/a
48	FOS	chr8:86494763-86494978	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr8:86526559-86526927	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr8:86544555-86544966	MCF10A-Er-Src	breast:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:86504072-86504122	ProgFib	skin:	n/a
2	chr8:86504072-86504122	PrEC	prostate:	n/a
3	chr8:86504072-86504122	HRCEpiC	kidney:	n/a
4	chr8:86486097-86486147	Hela-S3	cervix:	n/a
5	chr8:86504072-86504122	NHBE	bronchial:	n/a
6	chr8:86504072-86504122	AG09309	skin:	n/a
7	chr8:86486097-86486147	HNPCEpiC	eye:	n/a
8	chr8:86486097-86486147	NHBE	bronchial:	n/a
9	chr8:86486097-86486147	HRE	kidney:	n/a
10	chr8:86486097-86486147	SK-N-SH_RA	brain:	n/a
11	chr8:86504072-86504122	Hepatocyte	liver:	n/a
12	chr8:86504072-86504122	HCF	heart:	n/a
13	chr8:86486097-86486147	SK-N-MC	brain:	n/a
14	chr8:86486097-86486147	GM12892	blood:	n/a
15	chr8:86486097-86486147	HCT-116	colon:	n/a
16	chr8:86504072-86504122	HEK293	kidney:	embryo
17	chr8:86504072-86504122	PFSK-1	brain:	n/a
18	chr8:86504072-86504122	LNCaP	prostate:	n/a
19	chr8:86504072-86504122	BE2_C	brain:	n/a
20	chr8:86504072-86504122	H1-hESC	embryonic stem cell:	embryo
21	chr8:86504072-86504122	HepG2	liver:	n/a
22	chr8:86486097-86486147	HMEC	breast:	n/a
23	chr8:86486097-86486147	T-47D	breast:	n/a
24	chr8:86504072-86504122	K562	blood:	n/a
25	chr8:86486097-86486147	SAEC	small airway:	n/a
26	chr8:86486097-86486147	H1-hESC	embryonic stem cell:	embryo
27	chr8:86486097-86486147	HCPEpiC	choroid plexus:	n/a
28	chr8:86504072-86504122	AG09319	gingival:	n/a
29	chr8:86504072-86504122	RPTEC	kidney:	n/a
30	chr8:86486097-86486147	ProgFib	skin:	n/a
31	chr8:86504072-86504122	IMR90	lung:	fetal
32	chr8:86504072-86504122	GM12891	blood:	n/a
33	chr8:86504072-86504122	T-47D	breast:	n/a
34	chr8:86486097-86486147	PrEC	prostate:	n/a
35	chr8:86486097-86486147	GM19239	blood:	n/a
36	chr8:86486097-86486147	HAEpiC	amniotic membrane:	n/a
37	chr8:86486097-86486147	NH-A	brain:	n/a
38	chr8:86504072-86504122	AoSMC	blood vessel:	n/a
39	chr8:86504072-86504122	AG10803	skin:	n/a
40	chr8:86504072-86504122	HPAEpiC	pulmonary alveolar:	n/a
41	chr8:86486097-86486147	SK-N-SH	brain:	n/a
42	chr8:86486097-86486147	CMK	blood:	n/a
43	chr8:86504072-86504122	GM19239	blood:	n/a
44	chr8:86486097-86486147	HEEpiC	esophagus:	n/a
45	chr8:86504072-86504122	BJ	skin:	n/a
46	chr8:86486097-86486147	MCF10A-Er-Src	breast:	n/a
47	chr8:86504072-86504122	HUVEC	blood vessel:	n/a
48	chr8:86486097-86486147	HCF	heart:	n/a
49	chr8:86486097-86486147	GM12878	blood:	n/a
50	chr8:86504072-86504122	ovcar-3	ovarian:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:86494376..86498242-chr8:86499635..86502661,3	MCF-7	breast:
2	chr22:21257752..21260264-chr8:86546631..86548915,2	MCF-7	breast:
3	chr8:86494376..86498242-chr8:86499635..86502661,3	MCF-7	breast:
4	chr8:86375424..86377352-chr8:86545353..86547430,2	MCF-7	breast:
5	chr8:86439507..86442336-chr8:86514176..86515935,2	MCF-7	breast:
6	chr8:86525634..86527923-chr8:86533854..86535632,2	MCF-7	breast:
7	chr8:86482210..86485611-chr8:86487040..86489200,3	MCF-7	breast:
8	chr8:86482210..86485611-chr8:86487040..86489200,3	MCF-7	breast:
9	chr8:86375239..86377397-chr8:86481535..86484020,2	MCF-7	breast:
10	chr8:86374283..86376503-chr8:86538225..86540669,2	MCF-7	breast:
11	chr8:86525634..86527923-chr8:86533854..86535632,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-REXO1L1-3	chr8:86509528-86509569	NONHSAT127537
2	lnc-REXO1L1-3	chr8:86508349-86508606	NONHSAT127537

No data

Variant related genes	Relation type
ENSG00000253680	TF binding region
ENSG00000253680	CpG island
ENSG00000253549	chromatin interactions
ENSG00000104267	chromatin interactions

Extended variants
information (count: 1682 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1682 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149584181	chr8:86483958-86483959	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs188042170	chr8:86484049-86484050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs555537487	chr8:86484063-86484064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs113218103	chr8:86484109-86484110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs73265422	chr8:86484157-86484158	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs548493278	chr8:86484234-86484235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs568598617	chr8:86484287-86484288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs201452463	chr8:86484288-86484289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs568136014	chr8:86484309-86484310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs527499286	chr8:86484323-86484324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs547137233	chr8:86484339-86484340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs144307932	chr8:86484380-86484381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs148716672	chr8:86484406-86484407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs189801493	chr8:86484429-86484430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs141960448	chr8:86484442-86484443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs146260640	chr8:86484465-86484466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555264959	chr8:86484482-86484483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs574900676	chr8:86484495-86484496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs540828844	chr8:86484569-86484570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs139430365	chr8:86484575-86484576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs576921058	chr8:86484606-86484607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144083771	chr8:86484625-86484626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562523916	chr8:86484632-86484633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs183396068	chr8:86484635-86484636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs187790957	chr8:86484667-86484668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562028021	chr8:86484690-86484691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs527448978	chr8:86484701-86484702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs359532	chr8:86484755-86484756	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs570700338	chr8:86484857-86484858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376338758	chr8:86484882-86484883	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs359531	chr8:86484883-86484884	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs527842637	chr8:86484900-86484901	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs192233601	chr8:86484929-86484930	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561113266	chr8:86484986-86484987	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554923195	chr8:86484995-86484996	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs568736853	chr8:86485092-86485093	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs534268007	chr8:86485102-86485103	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185438252	chr8:86485131-86485132	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577056282	chr8:86485140-86485141	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545866913	chr8:86485169-86485170	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556256698	chr8:86485215-86485216	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373635955	chr8:86485227-86485228	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs576320289	chr8:86485239-86485240	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542209532	chr8:86485265-86485266	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs561987748	chr8:86485288-86485289	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs146480707	chr8:86485292-86485293	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs4740054	chr8:86485306-86485307	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs564249886	chr8:86485321-86485322	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs359530	chr8:86485358-86485359	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs549867501	chr8:86485425-86485426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Acute monocytic leukemia	16498392	CNVD
Autism	20841430	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:296 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:86480800-86487000	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr8:86481600-86485200	Weak transcription	Brain Anterior Caudate	brain
3	chr8:86481600-86486600	Weak transcription	Brain Cingulate Gyrus	brain
4	chr8:86481600-86486800	Weak transcription	Brain Angular Gyrus	brain
5	chr8:86482200-86484800	Weak transcription	Brain Hippocampus Middle	brain
6	chr8:86482200-86485000	Weak transcription	Brain Substantia Nigra	brain
7	chr8:86482400-86484400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr8:86482400-86485000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr8:86483200-86486200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr8:86483400-86484800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr8:86483800-86486200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr8:86484800-86485400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
13	chr8:86484800-86485400	Enhancers	Brain Hippocampus Middle	brain
14	chr8:86485000-86485400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr8:86485000-86488400	Enhancers	Brain Substantia Nigra	brain
16	chr8:86485200-86485400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr8:86485200-86488800	Enhancers	Brain Anterior Caudate	brain
18	chr8:86485400-86486000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr8:86485400-86486600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr8:86485400-86487200	Weak transcription	Brain Hippocampus Middle	brain
21	chr8:86485400-86488600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr8:86485400-86494000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
23	chr8:86486000-86488000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr8:86486200-86486400	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr8:86486200-86486800	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr8:86486200-86486800	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr8:86486200-86486800	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr8:86486200-86488000	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr8:86486200-86488600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr8:86486400-86487200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr8:86486600-86486800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr8:86486600-86488000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr8:86486600-86488800	Enhancers	Brain Cingulate Gyrus	brain
34	chr8:86486800-86487200	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr8:86486800-86487400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr8:86486800-86487400	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr8:86486800-86487800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr8:86486800-86488000	Enhancers	Brain Angular Gyrus	brain
39	chr8:86487000-86488200	Enhancers	Brain Inferior Temporal Lobe	brain
40	chr8:86487200-86487800	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr8:86487200-86488000	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr8:86487200-86488400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr8:86487200-86489000	Enhancers	Brain Hippocampus Middle	brain
44	chr8:86487400-86488000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr8:86487400-86488000	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr8:86487400-86488000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
47	chr8:86487600-86488400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr8:86487800-86488200	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr8:86487800-86488400	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr8:86487800-86488600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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