Variant report

Variant	nsv984554
Chromosome Location	chr8:90410700-90501154
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:400)
CpG islands
(count:61)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:400 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr8:90416009-90416315	GM12878	blood:	n/a	n/a
2	BATF	chr8:90415938-90416281	GM12878	blood:	n/a	chr8:90416131-90416142
3	BATF	chr8:90415981-90416338	GM12878	blood:	n/a	chr8:90416131-90416142
4	BCL11A	chr8:90454684-90454983	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr8:90415997-90416298	GM12878	blood:	n/a	n/a
6	BCL11A	chr8:90415990-90416356	GM12878	blood:	n/a	n/a
7	BRCA1	chr8:90486078-90486834	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr8:90486072-90486480	MCF-7	breast:	n/a	n/a
9	CEBPB	chr8:90447921-90448314	IMR90	lung:	n/a	chr8:90448136-90448147
10	CEBPB	chr8:90454684-90454966	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr8:90485956-90486449	MCF-7	breast:	n/a	n/a
12	CEBPB	chr8:90486029-90486718	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr8:90491820-90491877	HepG2	liver:	n/a	n/a
14	CEBPB	chr8:90479932-90480099	A549	lung:	n/a	n/a
15	CEBPB	chr8:90447965-90448285	HepG2	liver:	n/a	chr8:90448136-90448147
16	CEBPB	chr8:90438967-90439561	HCT-116	colon:	n/a	chr8:90439489-90439502
17	CEBPB	chr8:90454226-90454367	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr8:90486060-90486450	IMR90	lung:	n/a	n/a
19	CEBPB	chr8:90485991-90486501	HCT-116	colon:	n/a	n/a
20	CEBPB	chr8:90425760-90425857	HepG2	liver:	n/a	n/a
21	CEBPB	chr8:90454220-90454409	HepG2	liver:	n/a	n/a
22	CEBPB	chr8:90486077-90486548	A549	lung:	n/a	n/a
23	CEBPB	chr8:90479862-90480124	MCF-7	breast:	n/a	n/a
24	CEBPB	chr8:90485935-90486613	HCT-116	colon:	n/a	n/a
25	CREB1	chr8:90415987-90416329	GM12878	blood:	n/a	n/a
26	CREB1	chr8:90415944-90416460	GM12878	blood:	n/a	n/a
27	CTCF	chr8:90425010-90425198	HepG2	liver:	n/a	n/a
28	CTCF	chr8:90425721-90425818	MCF-7	breast:	n/a	n/a
29	CTCF	chr8:90463787-90463897	GM10266	blood:	n/a	n/a
30	CTCF	chr8:90425067-90425195	GM19240	blood:	n/a	n/a
31	CTCF	chr8:90425080-90425230	MCF-7	breast:	n/a	n/a
32	CTCF	chr8:90425736-90425843	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr8:90425040-90425190	AG04449	skin:	n/a	n/a
34	CTCF	chr8:90425033-90425237	MCF-7	breast:	n/a	n/a
35	CTCF	chr8:90425680-90425830	HepG2	liver:	n/a	n/a
36	CTCF	chr8:90425034-90425233	MCF-7	breast:	n/a	n/a
37	CTCF	chr8:90425000-90425150	GM12875	blood:	n/a	n/a
38	CTCF	chr8:90425060-90425210	GM12871	blood:	n/a	n/a
39	CTCF	chr8:90425700-90425850	Caco-2	colon:	n/a	n/a
40	CTCF	chr8:90425100-90425250	HepG2	liver:	n/a	n/a
41	CTCF	chr8:90425080-90425230	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr8:90425079-90425230	GM19239	blood:	n/a	n/a
43	CTCF	chr8:90424980-90425130	NB4	blood:	n/a	n/a
44	CTCF	chr8:90424960-90425110	GM12872	blood:	n/a	n/a
45	CTCF	chr8:90425080-90425230	GM12866	blood:	n/a	n/a
46	CTCF	chr8:90425020-90425170	GM12878	blood:	n/a	n/a
47	CTCF	chr8:90425733-90425820	GM12891	blood:	n/a	n/a
48	CTCF	chr8:90425672-90425848	HepG2	liver:	n/a	n/a
49	CTCF	chr8:90479558-90479595	GM19239	blood:	n/a	n/a
50	CTCF	chr8:90425039-90425206	GM12892	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:90427508-90427558	PrEC	prostate:	n/a
2	chr8:90427508-90427558	PFSK-1	brain:	n/a
3	chr8:90427508-90427558	A549	lung:	n/a
4	chr8:90427508-90427558	HRE	kidney:	n/a
5	chr8:90427508-90427558	ECC-1	luminal epithelium:	n/a
6	chr8:90427508-90427558	AoSMC	blood vessel:	n/a
7	chr8:90427508-90427558	AG09319	gingival:	n/a
8	chr8:90427508-90427558	NT2-D1	testis:	n/a
9	chr8:90427508-90427558	HUVEC	blood vessel:	n/a
10	chr8:90427508-90427558	HCM	heart:	n/a
11	chr8:90427508-90427558	PANC-1	pancreas:	n/a
12	chr8:90427508-90427558	LNCaP	prostate:	n/a
13	chr8:90427508-90427558	H1-hESC	embryonic stem cell:	embryo
14	chr8:90427508-90427558	HCT-116	colon:	n/a
15	chr8:90427508-90427558	NHDF-neo	bronchial:	n/a
16	chr8:90427508-90427558	HCPEpiC	choroid plexus:	n/a
17	chr8:90427508-90427558	RPTEC	kidney:	n/a
18	chr8:90427508-90427558	SKMC	muscle:	n/a
19	chr8:90427508-90427558	HPAEpiC	pulmonary alveolar:	n/a
20	chr8:90427508-90427558	AG10803	skin:	n/a
21	chr8:90427508-90427558	HNPCEpiC	eye:	n/a
22	chr8:90427508-90427558	NH-A	brain:	n/a
23	chr8:90427508-90427558	T-47D	breast:	n/a
24	chr8:90427508-90427558	Hepatocyte	liver:	n/a
25	chr8:90427508-90427558	BJ	skin:	n/a
26	chr8:90427508-90427558	HMEC	breast:	n/a
27	chr8:90427508-90427558	HL-60	blood:	n/a
28	chr8:90427508-90427558	SK-N-SH_RA	brain:	n/a
29	chr8:90427508-90427558	GM12892	blood:	n/a
30	chr8:90427508-90427558	GM19239	blood:	n/a
31	chr8:90427508-90427558	AG04449	skin:	fetal
32	chr8:90427508-90427558	HRPEpiC	eye:	n/a
33	chr8:90427508-90427558	MCF-7	breast:	n/a
34	chr8:90427508-90427558	GM12891	blood:	n/a
35	chr8:90427508-90427558	ovcar-3	ovarian:	n/a
36	chr8:90427508-90427558	Caco-2	colon:	n/a
37	chr8:90427508-90427558	NB4	blood:	n/a
38	chr8:90427508-90427558	CMK	blood:	n/a
39	chr8:90427508-90427558	HAEpiC	amniotic membrane:	n/a
40	chr8:90427508-90427558	K562	blood:	n/a
41	chr8:90427508-90427558	AG04450	lung:	fetal
42	chr8:90427508-90427558	HIPEpiC	eye:	n/a
43	chr8:90427508-90427558	U87	brain:	n/a
44	chr8:90427508-90427558	ProgFib	skin:	n/a
45	chr8:90427508-90427558	NHBE	bronchial:	n/a
46	chr8:90427508-90427558	BE2_C	brain:	n/a
47	chr8:90427508-90427558	IMR90	lung:	fetal
48	chr8:90427508-90427558	HepG2	liver:	n/a
49	chr8:90427508-90427558	Hela-S3	cervix:	n/a
50	chr8:90427508-90427558	HCF	heart:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:90481059..90483320-chr8:90483632..90486597,2	MCF-7	breast:
2	chr8:90476514..90479734-chr8:90482922..90486651,5	MCF-7	breast:
3	chr8:90443469..90445041-chr8:90445862..90447518,2	MCF-7	breast:
4	chr8:90437468..90439061-chr8:90443670..90445769,2	MCF-7	breast:
5	chr8:90497830..90499463-chr8:90622312..90625050,2	MCF-7	breast:
6	chr20:46130384..46130956-chr8:90423490..90424387,2	MCF-7	breast:
7	chr8:90409960..90412436-chr8:90413000..90414857,2	MCF-7	breast:
8	chr8:90443469..90445041-chr8:90445862..90447518,2	MCF-7	breast:
9	chr8:90402877..90404384-chr8:90409291..90411410,2	MCF-7	breast:
10	chr8:90476514..90479734-chr8:90482922..90486651,5	MCF-7	breast:
11	chr1:208136517..208137331-chr8:90485310..90486252,2	MCF-7	breast:
12	chr8:90437468..90439061-chr8:90443670..90445769,2	MCF-7	breast:
13	chr8:90409960..90412436-chr8:90413000..90414857,2	MCF-7	breast:
14	chr8:90481059..90483320-chr8:90483632..90486597,2	MCF-7	breast:
15	chr8:90424990..90426276-chr8:90629028..90629951,3	MCF-7	breast:
16	chr8:90427557..90429111-chr8:90431047..90432856,2	MCF-7	breast:
17	chr8:90427557..90429111-chr8:90431047..90432856,2	MCF-7	breast:

No data

Variant related genes	Relation type
KRT8P4	TF binding region
KRT8P4	CpG island
ENSG00000251136	chromatin interactions
ENSG00000124151	chromatin interactions

Extended variants
information (count: 3637 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:3637 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77033407	chr8:90410716-90410717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs532491044	chr8:90410837-90410838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs547817378	chr8:90410876-90410877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138106752	chr8:90410883-90410884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs35799383	chr8:90410913-90410914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs188803831	chr8:90410926-90410927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs527617543	chr8:90410936-90410937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548829520	chr8:90410946-90410947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs567145076	chr8:90410955-90410956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs375438440	chr8:90411002-90411003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs74605177	chr8:90411009-90411010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs549473106	chr8:90411065-90411066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs28685057	chr8:90411072-90411073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs181640927	chr8:90411074-90411075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs571463788	chr8:90411170-90411171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185470154	chr8:90411182-90411183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs553857899	chr8:90411189-90411190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs571915916	chr8:90411222-90411223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs58524292	chr8:90411229-90411230	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs555257112	chr8:90411236-90411237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs118139755	chr8:90411240-90411241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs544070959	chr8:90411243-90411244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs559192487	chr8:90411265-90411266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535859422	chr8:90411295-90411296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs112836408	chr8:90411299-90411300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs111714889	chr8:90411342-90411343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs541150521	chr8:90411354-90411355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs559712333	chr8:90411406-90411407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190345726	chr8:90411428-90411429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs182226247	chr8:90411465-90411466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555598497	chr8:90411485-90411486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs143879373	chr8:90411513-90411514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549608181	chr8:90411526-90411527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs148607122	chr8:90411554-90411555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs78616132	chr8:90411558-90411559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186270476	chr8:90411579-90411580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs544551082	chr8:90411585-90411586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs66847521	chr8:90411621-90411622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs376205527	chr8:90411622-90411623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs28393310	chr8:90411637-90411638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs6150695	chr8:90411645-90411646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189608730	chr8:90411646-90411647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs369738511	chr8:90411759-90411760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs565674956	chr8:90411809-90411810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs536215596	chr8:90411828-90411829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554596053	chr8:90411861-90411862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs554734235	chr8:90411878-90411879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs116814051	chr8:90411879-90411880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs180911033	chr8:90411912-90411913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374119171	chr8:90411917-90411918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

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
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
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
Breast cancer	21611746	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:178 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:90394000-90414800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:90414800-90415200	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr8:90414800-90416200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr8:90414800-90416200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr8:90415600-90427200	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr8:90416000-90417000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr8:90416200-90416600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr8:90416200-90416600	Enhancers	Muscle Satellite Cultured Cells	--
9	chr8:90416200-90419000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr8:90416600-90416800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr8:90416800-90417000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr8:90417000-90417400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr8:90417400-90420000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr8:90419600-90419800	Enhancers	NHDF-Ad	bronchial
15	chr8:90419800-90420800	Weak transcription	NHDF-Ad	bronchial
16	chr8:90420000-90420600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr8:90420600-90421000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr8:90420800-90421600	Enhancers	NHDF-Ad	bronchial
19	chr8:90420800-90422200	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr8:90421000-90421600	Enhancers	H9 Cell Line	embryonic stem cell
21	chr8:90421000-90421600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr8:90421000-90421600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr8:90421000-90421800	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr8:90421000-90421800	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr8:90421000-90421800	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr8:90421000-90422200	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr8:90421000-90422400	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr8:90421200-90421600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr8:90421200-90421800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr8:90421400-90421600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr8:90421600-90427000	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr8:90421600-90430600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr8:90421800-90427400	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr8:90422200-90427400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr8:90422400-90425800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr8:90422400-90427200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr8:90422600-90425200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr8:90424000-90424400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr8:90424400-90435200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr8:90424800-90426600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr8:90425000-90426400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr8:90425200-90425400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
43	chr8:90425200-90425600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr8:90425400-90425600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr8:90425400-90427800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
46	chr8:90425800-90427000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
47	chr8:90426800-90427000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr8:90427000-90427400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr8:90427000-90428200	Enhancers	H9 Cell Line	embryonic stem cell
50	chr8:90427200-90428200	Enhancers	H1 Cell Line	embryonic stem cell

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