Variant report

Variant	nsv891176
Chromosome Location	chr8:89731444-89856254
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:302)
CpG islands
(count:184)
Chromatin interactive
region (count:24)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:302 , 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	chr8:89799915-89800095	K562	blood:	n/a	n/a
2	BACH1	chr8:89792855-89792956	K562	blood:	n/a	n/a
3	BATF	chr8:89851958-89852146	GM12878	blood:	n/a	n/a
4	BATF	chr8:89851926-89852130	GM12878	blood:	n/a	n/a
5	BHLHE40	chr8:89761792-89761832	K562	blood:	n/a	n/a
6	CBX3	chr8:89735805-89736242	HCT-116	colon:	n/a	n/a
7	CBX3	chr8:89735838-89736363	HCT-116	colon:	n/a	n/a
8	CEBPB	chr8:89793800-89793892	A549	lung:	n/a	n/a
9	CEBPB	chr8:89855829-89856039	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr8:89759890-89760192	IMR90	lung:	n/a	chr8:89760024-89760035
11	CEBPB	chr8:89759879-89760191	HepG2	liver:	n/a	chr8:89760024-89760035
12	CEBPB	chr8:89741569-89741757	MCF-7	breast:	n/a	chr8:89741649-89741658
13	CEBPB	chr8:89759944-89760190	A549	lung:	n/a	chr8:89760024-89760035
14	CEBPB	chr8:89815880-89815985	HepG2	liver:	n/a	chr8:89815931-89815942 chr8:89815930-89815943
15	CTCF	chr8:89823985-89824075	Fibrobl	skin:	n/a	n/a
16	CTCF	chr8:89819420-89819570	HRE	kidney:	n/a	n/a
17	CTCF	chr8:89823953-89824105	ProgFib	skin:	n/a	n/a
18	CTCF	chr8:89823880-89824030	HCT-116	colon:	n/a	n/a
19	CTCF	chr8:89823900-89824050	HFF-Myc	foreskin:	n/a	n/a
20	CTCF	chr8:89755414-89755477	GM10266	blood:	n/a	n/a
21	CTCF	chr8:89823980-89824130	SAEC	small airway:	n/a	n/a
22	CTCF	chr8:89775213-89775298	Lung_OC	lung:	n/a	n/a
23	CTCF	chr8:89824080-89824230	A549	lung:	n/a	n/a
24	CTCF	chr8:89823940-89824090	Caco-2	colon:	n/a	n/a
25	CTCF	chr8:89823920-89824070	HCT-116	colon:	n/a	n/a
26	CTCF	chr8:89823900-89824050	RPTEC	kidney:	n/a	n/a
27	CTCF	chr8:89841760-89841910	MCF-7	breast:	n/a	n/a
28	CTCF	chr8:89763880-89764030	GM12867	blood:	n/a	n/a
29	CTCF	chr8:89764060-89764210	SAEC	small airway:	n/a	n/a
30	CTCF	chr8:89855956-89856098	MCF-7	breast:	n/a	n/a
31	CTCF	chr8:89823920-89824070	AoAF	blood vessel:	n/a	n/a
32	CTCF	chr8:89764315-89764467	MCF-7	breast:	n/a	n/a
33	CTCF	chr8:89823884-89824342	HCT-116	colon:	n/a	n/a
34	CTCF	chr8:89855948-89856089	MCF-7	breast:	n/a	n/a
35	CTCF	chr8:89823980-89824130	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr8:89824000-89824150	SAEC	small airway:	n/a	n/a
37	CTCF	chr8:89847120-89847270	HMEC	breast:	n/a	n/a
38	CTCF	chr8:89764380-89764530	HEK293	kidney:	n/a	n/a
39	CTCF	chr8:89855900-89856050	MCF-7	breast:	n/a	n/a
40	CTCF	chr8:89823980-89824130	GM12872	blood:	n/a	n/a
41	CTCF	chr8:89823960-89824110	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr8:89752479-89752549	LNCaP	prostate:	n/a	n/a
43	CTCF	chr8:89855880-89856030	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr8:89855900-89856050	HEEpiC	esophagus:	n/a	n/a
45	CTCF	chr8:89824000-89824150	HMEC	breast:	n/a	n/a
46	CTCF	chr8:89855954-89856085	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr8:89823944-89824090	MCF-7	breast:	n/a	n/a
48	CTCF	chr8:89823960-89824110	HFF	foreskin:	n/a	n/a
49	CTCF	chr8:89823980-89824130	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr8:89855880-89856030	HCPEpiC	choroid plexus:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:89856205-89856255	GM12878	blood:	n/a
2	chr8:89856205-89856255	GM12878	blood:	n/a
3	chr8:89777219-89777269	SKMC	muscle:	n/a
4	chr8:89747827-89747877	HCF	heart:	n/a
5	chr8:89747827-89747877	IMR90	lung:	fetal
6	chr8:89777219-89777269	HPAEpiC	pulmonary alveolar:	n/a
7	chr8:89777219-89777269	HMEC	breast:	n/a
8	chr8:89777219-89777269	IMR90	lung:	fetal
9	chr8:89856205-89856255	HMEC	breast:	n/a
10	chr8:89856205-89856255	T-47D	breast:	n/a
11	chr8:89856205-89856255	PFSK-1	brain:	n/a
12	chr8:89777219-89777269	AG04449	skin:	fetal
13	chr8:89747827-89747877	SK-N-MC	brain:	n/a
14	chr8:89777219-89777269	SK-N-SH	brain:	n/a
15	chr8:89777219-89777269	GM12891	blood:	n/a
16	chr8:89777219-89777269	PANC-1	pancreas:	n/a
17	chr8:89777219-89777269	HAEpiC	amniotic membrane:	n/a
18	chr8:89747827-89747877	HUVEC	blood vessel:	n/a
19	chr8:89747827-89747877	MCF10A-Er-Src	breast:	n/a
20	chr8:89777219-89777269	NB4	blood:	n/a
21	chr8:89747827-89747877	HepG2	liver:	n/a
22	chr8:89777219-89777269	CMK	blood:	n/a
23	chr8:89856205-89856255	PrEC	prostate:	n/a
24	chr8:89777219-89777269	Hepatocyte	liver:	n/a
25	chr8:89747827-89747877	GM12878	blood:	n/a
26	chr8:89856205-89856255	GM06990	blood:	n/a
27	chr8:89856205-89856255	HEK293	kidney:	embryo
28	chr8:89777219-89777269	H1-hESC	embryonic stem cell:	embryo
29	chr8:89856205-89856255	NB4	blood:	n/a
30	chr8:89856205-89856255	Hepatocyte	liver:	n/a
31	chr8:89777219-89777269	LNCaP	prostate:	n/a
32	chr8:89747827-89747877	SAEC	small airway:	n/a
33	chr8:89747827-89747877	SK-N-SH	brain:	n/a
34	chr8:89856205-89856255	BE2_C	brain:	n/a
35	chr8:89856205-89856255	SAEC	small airway:	n/a
36	chr8:89747827-89747877	GM12891	blood:	n/a
37	chr8:89747827-89747877	HMEC	breast:	n/a
38	chr8:89777219-89777269	BE2_C	brain:	n/a
39	chr8:89777219-89777269	T-47D	breast:	n/a
40	chr8:89777219-89777269	HRPEpiC	eye:	n/a
41	chr8:89777219-89777269	HEEpiC	esophagus:	n/a
42	chr8:89777219-89777269	A549	lung:	n/a
43	chr8:89777219-89777269	HRE	kidney:	n/a
44	chr8:89777219-89777269	HCT-116	colon:	n/a
45	chr8:89747827-89747877	HEK293	kidney:	embryo
46	chr8:89856205-89856255	HepG2	liver:	n/a
47	chr8:89856205-89856255	ovcar-3	ovarian:	n/a
48	chr8:89777219-89777269	NH-A	brain:	n/a
49	chr8:89777219-89777269	AoSMC	blood vessel:	n/a
50	chr8:89856205-89856255	U87	brain:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:89566591..89567525-chr8:89823590..89824198,2	MCF-7	breast:
2	chr8:89739274..89741263-chr8:89742331..89745180,2	K562	blood:
3	chr8:89795626..89797821-chr8:89798441..89801193,3	MCF-7	breast:
4	chr8:89725334..89726635-chr8:89823867..89824656,3	MCF-7	breast:
5	chr8:89752103..89756050-chr8:89761305..89763594,3	K562	blood:
6	chr8:89848601..89851264-chr8:89852497..89854514,2	MCF-7	breast:
7	chr8:89848601..89851264-chr8:89852497..89854514,2	MCF-7	breast:
8	chr8:89739274..89741263-chr8:89742331..89745180,2	K562	blood:
9	chr8:89340717..89341497-chr8:89823523..89824135,2	MCF-7	breast:
10	chr8:89809461..89810989-chr8:89814329..89816042,2	K562	blood:
11	chr8:89826530..89828949-chr8:89832664..89834256,2	MCF-7	breast:
12	chr8:89752103..89756050-chr8:89761305..89763594,3	K562	blood:
13	chr8:89809461..89810989-chr8:89814329..89816042,2	K562	blood:
14	chr8:89724996..89725850-chr8:89855566..89856466,2	MCF-7	breast:
15	chr8:89795626..89797821-chr8:89798441..89801193,3	MCF-7	breast:
16	chr8:89739665..89742601-chr8:89745667..89747250,2	MCF-7	breast:
17	chr8:89739665..89742601-chr8:89745667..89747250,2	MCF-7	breast:
18	chr21:47742904..47745243-chr8:89801334..89803902,2	MCF-7	breast:
19	chr8:89826530..89828949-chr8:89832664..89834256,2	MCF-7	breast:
20	chr8:89794068..89795764-chr8:89807097..89809455,2	MCF-7	breast:
21	chr8:89818784..89820369-chr8:89820936..89822501,2	MCF-7	breast:
22	chr8:89814209..89816612-chr8:89819273..89821915,2	K562	blood:
23	chr8:89794068..89795764-chr8:89807097..89809455,2	MCF-7	breast:
24	chr8:89304192..89305173-chr8:89823627..89824192,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MMP16-4	chr8:89820547-89821137	ENSG00000271156.1
2	lnc-CNBD1-4	chr8:89747954-89749363	ENSG00000253553.1
3	lnc-CNBD1-4	chr8:89748095-89749363	NONHSAT127604

No data

Variant related genes	Relation type
ENSG00000271156	TF binding region
ENSG00000271156	CpG island
ENSG00000160299	chromatin interactions
ENSG00000160298	chromatin interactions
ENSG00000271156	chromatin interactions

Extended variants
information (count: 1012 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:1012 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548362823	chr8:89742304-89742305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs569111846	chr8:89742471-89742472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs539970881	chr8:89742474-89742475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs142536806	chr8:89742489-89742490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs62525848	chr8:89742585-89742586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs569936035	chr8:89742602-89742603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs536918892	chr8:89742603-89742604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs371875189	chr8:89742606-89742607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs558538947	chr8:89742638-89742639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs576798922	chr8:89742645-89742646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs13249157	chr8:89742657-89742658	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs552689820	chr8:89742668-89742669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs574190508	chr8:89742716-89742717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs200825717	chr8:89742747-89742748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs542020491	chr8:89742758-89742759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs538801087	chr8:89742781-89742782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs563688086	chr8:89742812-89742813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs200363416	chr8:89742850-89742851	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs201559143	chr8:89742851-89742852	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs115578604	chr8:89742913-89742914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs546210104	chr8:89742931-89742932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs114521726	chr8:89742947-89742948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs528537570	chr8:89742960-89742961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs541029878	chr8:89742970-89742971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs547016016	chr8:89743054-89743055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562168744	chr8:89743062-89743063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs529366858	chr8:89743070-89743071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189766041	chr8:89743114-89743115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs368045438	chr8:89743157-89743158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569723514	chr8:89743238-89743239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372125128	chr8:89743266-89743267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs79334135	chr8:89743283-89743284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs552222292	chr8:89743289-89743290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs74979403	chr8:89743310-89743311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs534361022	chr8:89743333-89743334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs76949954	chr8:89743338-89743339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs75126573	chr8:89743455-89743456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs535140704	chr8:89743480-89743481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs116462367	chr8:89743485-89743486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531531770	chr8:89743512-89743513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs573111994	chr8:89743683-89743684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575785946	chr8:89743707-89743708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546371348	chr8:89743714-89743715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs11984735	chr8:89743716-89743717	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs573532114	chr8:89743723-89743724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs182169496	chr8:89743742-89743743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs562029319	chr8:89743809-89743810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555866618	chr8:89743816-89743817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529428696	chr8:89743825-89743826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544406297	chr8:89743871-89743872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:108)

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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Schizophrenia	23813976	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:89742200-89742800	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr8:89742200-89743000	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr8:89742400-89743000	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr8:89743000-89747000	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr8:89744800-89745600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr8:89747000-89747800	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr8:89747000-89747800	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr8:89752400-89753000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr8:89756400-89757800	Active TSS	ES-I3 Cell Line	embryonic stem cell
10	chr8:89757200-89757800	Active TSS	H9 Cell Line	embryonic stem cell
11	chr8:89762800-89763600	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr8:89763800-89764200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr8:89763800-89764400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr8:89763800-89764400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr8:89763800-89764400	Enhancers	HMEC	breast
16	chr8:89764000-89764600	Enhancers	H1 Cell Line	embryonic stem cell
17	chr8:89764000-89764800	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr8:89777000-89778200	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr8:89777200-89778200	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr8:89777600-89778000	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr8:89777600-89778000	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr8:89777800-89778200	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr8:89777800-89778200	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr8:89811400-89812000	Enhancers	Fetal Brain Male	brain
25	chr8:89812800-89813200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr8:89821200-89821400	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr8:89823600-89823800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr8:89823600-89823800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr8:89823800-89824000	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr8:89823800-89825000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr8:89833600-89834400	Enhancers	Fetal Heart	heart
32	chr8:89835600-89836200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr8:89853800-89854000	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr8:89854200-89855400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr8:89855400-89856400	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr8:89855400-89856400	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr8:89855400-89856600	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr8:89855600-89856400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr8:89855600-89856400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr8:89855600-89856600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr8:89855600-89856600	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr8:89855800-89856200	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr8:89855800-89856600	Enhancers	ES-I3 Cell Line	embryonic stem cell

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