Variant report

Variant	nsv891369
Chromosome Location	chr8:115335219-115455967
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:208)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:208 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:115441617-115441711	K562	blood:	n/a	n/a
2	BATF	chr8:115451366-115451632	GM12878	blood:	n/a	n/a
3	BATF	chr8:115447401-115447735	GM12878	blood:	n/a	n/a
4	BATF	chr8:115451370-115451612	GM12878	blood:	n/a	n/a
5	BATF	chr8:115447376-115447721	GM12878	blood:	n/a	n/a
6	BRCA1	chr8:115400344-115401027	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr8:115336098-115336490	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr8:115363238-115363247	K562	blood:	n/a	n/a
9	CEBPB	chr8:115364696-115364815	A549	lung:	n/a	chr8:115364727-115364738 chr8:115364728-115364737 chr8:115364726-115364737 chr8:115364726-115364739
10	CEBPB	chr8:115364657-115364877	HepG2	liver:	n/a	chr8:115364727-115364738 chr8:115364728-115364737 chr8:115364726-115364737 chr8:115364726-115364739
11	CEBPB	chr8:115399635-115400913	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr8:115361911-115362139	HepG2	liver:	n/a	n/a
13	CEBPB	chr8:115400443-115400469	A549	lung:	n/a	n/a
14	CHD2	chr8:115343589-115343696	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr8:115370571-115370644	LNCaP	prostate:	n/a	n/a
16	CTCF	chr8:115450685-115450752	Hela-S3	cervix:	n/a	chr8:115450720-115450741 chr8:115450718-115450736
17	CTCF	chr8:115406610-115406664	Lung_OC	lung:	n/a	n/a
18	CTCF	chr8:115357491-115357533	GM10248	blood:	n/a	n/a
19	CTCF	chr8:115450639-115450824	MCF-7	breast:	n/a	chr8:115450720-115450741 chr8:115450718-115450736
20	CTCF	chr8:115341549-115341599	GM20000	blood:	n/a	n/a
21	CTCF	chr8:115450470-115450510	Kidney_OC	kidney:	n/a	n/a
22	CTCF	chr8:115414960-115415110	AG09309	skin:	n/a	n/a
23	CTCF	chr8:115423780-115423930	GM12873	blood:	n/a	n/a
24	CTCF	chr8:115450620-115450770	MCF-7	breast:	n/a	chr8:115450720-115450741 chr8:115450718-115450736
25	CTCF	chr8:115451413-115451648	GM12878	blood:	n/a	n/a
26	CTCF	chr8:115450840-115450990	HEEpiC	esophagus:	n/a	n/a
27	CTCF	chr8:115403267-115403308	LNCaP	prostate:	n/a	n/a
28	CTCF	chr8:115386660-115386810	HPAF	blood vessel:	n/a	n/a
29	CTCF	chr8:115448700-115448850	NHLF	lung:	n/a	chr8:115448772-115448780
30	CTCF	chr8:115453024-115453093	MCF-7	breast:	n/a	n/a
31	CTCF	chr8:115340764-115340863	GM20000	blood:	n/a	n/a
32	CTCF	chr8:115450686-115450786	HepG2	liver:	n/a	chr8:115450720-115450741 chr8:115450718-115450736
33	CTCF	chr8:115450660-115450810	WERI-Rb-1	eye:	n/a	chr8:115450720-115450741 chr8:115450718-115450736
34	CTCF	chr8:115450656-115450814	MCF-7	breast:	n/a	chr8:115450720-115450741 chr8:115450718-115450736
35	CTCF	chr8:115360785-115360827	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr8:115450680-115450830	Hela-S3	cervix:	n/a	chr8:115450720-115450741 chr8:115450718-115450736
37	CTCF	chr8:115403234-115403321	LNCaP	prostate:	n/a	n/a
38	CUX1	chr8:115355462-115355517	GM12878	blood:	n/a	n/a
39	CUX1	chr8:115410578-115410795	GM12878	blood:	n/a	n/a
40	E2F4	chr8:115352313-115352397	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr8:115338846-115338992	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr8:115408639-115408887	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr8:115355477-115355532	GM12878	blood:	n/a	n/a
44	E2F4	chr8:115434930-115435095	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr8:115437864-115438068	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr8:115347794-115348054	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr8:115416549-115416688	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr8:115376729-115376846	MCF10A-Er-Src	breast:	n/a	n/a
49	EBF1	chr8:115410685-115410806	GM12878	blood:	n/a	n/a
50	EBF1	chr8:115336340-115336615	GM12878	blood:	n/a	chr8:115336482-115336493

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:115398676-115398726	NB4	blood:	n/a
2	chr8:115398676-115398726	GM06990	blood:	n/a
3	chr8:115398676-115398726	PANC-1	pancreas:	n/a
4	chr8:115398676-115398726	AG04449	skin:	fetal
5	chr8:115398676-115398726	U87	brain:	n/a
6	chr8:115398676-115398726	LNCaP	prostate:	n/a
7	chr8:115398676-115398726	HRE	kidney:	n/a
8	chr8:115398676-115398726	Caco-2	colon:	n/a
9	chr8:115398676-115398726	GM12892	blood:	n/a
10	chr8:115398676-115398726	ECC-1	luminal epithelium:	n/a
11	chr8:115398676-115398726	HL-60	blood:	n/a
12	chr8:115398676-115398726	T-47D	breast:	n/a
13	chr8:115398676-115398726	RPTEC	kidney:	n/a
14	chr8:115398676-115398726	HUVEC	blood vessel:	n/a
15	chr8:115398676-115398726	BJ	skin:	n/a
16	chr8:115398676-115398726	PFSK-1	brain:	n/a
17	chr8:115398676-115398726	SKMC	muscle:	n/a
18	chr8:115398676-115398726	MCF10A-Er-Src	breast:	n/a
19	chr8:115398676-115398726	GM19239	blood:	n/a
20	chr8:115398676-115398726	MCF-7	breast:	n/a
21	chr8:115398676-115398726	GM12878	blood:	n/a
22	chr8:115398676-115398726	ovcar-3	ovarian:	n/a
23	chr8:115398676-115398726	HCT-116	colon:	n/a
24	chr8:115398676-115398726	HCF	heart:	n/a
25	chr8:115398676-115398726	K562	blood:	n/a
26	chr8:115398676-115398726	HCPEpiC	choroid plexus:	n/a
27	chr8:115398676-115398726	Hepatocyte	liver:	n/a
28	chr8:115398676-115398726	SAEC	small airway:	n/a
29	chr8:115398676-115398726	NT2-D1	testis:	n/a
30	chr8:115398676-115398726	A549	lung:	n/a
31	chr8:115398676-115398726	HEK293	kidney:	embryo
32	chr8:115398676-115398726	AoSMC	blood vessel:	n/a
33	chr8:115398676-115398726	AG10803	skin:	n/a
34	chr8:115398676-115398726	ProgFib	skin:	n/a
35	chr8:115398676-115398726	AG09309	skin:	n/a
36	chr8:115398676-115398726	HPAEpiC	pulmonary alveolar:	n/a
37	chr8:115398676-115398726	AG04450	lung:	fetal
38	chr8:115398676-115398726	Jurkat	blood:	n/a
39	chr8:115398676-115398726	HNPCEpiC	eye:	n/a
40	chr8:115398676-115398726	PrEC	prostate:	n/a
41	chr8:115398676-115398726	CMK	blood:	n/a
42	chr8:115398676-115398726	IMR90	lung:	fetal
43	chr8:115398676-115398726	HRPEpiC	eye:	n/a
44	chr8:115398676-115398726	NHBE	bronchial:	n/a
45	chr8:115398676-115398726	SK-N-MC	brain:	n/a
46	chr8:115398676-115398726	HMEC	breast:	n/a
47	chr8:115398676-115398726	GM12891	blood:	n/a
48	chr8:115398676-115398726	HEEpiC	esophagus:	n/a
49	chr8:115398676-115398726	H1-hESC	embryonic stem cell:	embryo
50	chr8:115398676-115398726	HIPEpiC	eye:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:115360876..115362417-chr8:115396298..115399107,2	K562	blood:
2	chr8:115392553..115395092-chr8:115402142..115404171,2	MCF-7	breast:
3	chr8:115360876..115362417-chr8:115396298..115399107,2	K562	blood:
4	chr8:115333482..115335799-chr8:115336000..115338063,2	K562	blood:
5	chr8:115333482..115335799-chr8:115336000..115338063,2	K562	blood:
6	chr8:115392553..115395092-chr8:115402142..115404171,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000253499	TF binding region
ENSG00000253499	CpG island

Extended variants
information (count: 1109 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1109 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10108383	chr8:115335219-115335220	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs181819989	chr8:115335234-115335235	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs568549016	chr8:115335254-115335255	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs543930895	chr8:115335278-115335279	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs368035337	chr8:115335310-115335311	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs565316623	chr8:115335382-115335383	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs117451638	chr8:115335405-115335406	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs541321551	chr8:115335425-115335426	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs74359017	chr8:115335437-115335438	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs76434905	chr8:115335438-115335439	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs559621644	chr8:115335446-115335447	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs537608381	chr8:115335475-115335476	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs527265170	chr8:115335615-115335616	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs143401150	chr8:115335625-115335626	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs560581397	chr8:115335639-115335640	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs6995822	chr8:115335720-115335721	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs186416200	chr8:115335770-115335771	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs115009327	chr8:115335772-115335773	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs6999686	chr8:115335837-115335838	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs190964888	chr8:115335838-115335839	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs118176947	chr8:115335861-115335862	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536617341	chr8:115335907-115335908	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs6981862	chr8:115335913-115335914	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs181604605	chr8:115335950-115335951	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186781067	chr8:115335962-115335963	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537147846	chr8:115335977-115335978	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs7462625	chr8:115336049-115336050	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs559018409	chr8:115336148-115336149	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs577317124	chr8:115336164-115336165	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs541630972	chr8:115336180-115336181	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs191378267	chr8:115336201-115336202	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574776715	chr8:115336240-115336241	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542144728	chr8:115336284-115336285	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs577793282	chr8:115336319-115336320	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs560542770	chr8:115336347-115336348	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs557030839	chr8:115336373-115336374	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs183208314	chr8:115336375-115336376	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549571809	chr8:115336434-115336435	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs564995996	chr8:115336564-115336565	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs10955703	chr8:115336575-115336576	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs547628527	chr8:115336611-115336612	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs10112505	chr8:115336693-115336694	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs78415691	chr8:115336721-115336722	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186701854	chr8:115336759-115336760	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542223959	chr8:115336763-115336764	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs189980038	chr8:115336792-115336793	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs537453659	chr8:115336797-115336798	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs373681368	chr8:115336822-115336823	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs572486797	chr8:115336834-115336835	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs570936352	chr8:115336882-115336883	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	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
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
Glioblastoma multiforme	21080181	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
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	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
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
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21364760	CNVD
Neuroticism	17667963	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Schizophrenia	23813976	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:115334800-115337000	Enhancers	Dnd41	blood
2	chr8:115335000-115335400	Enhancers	GM12878-XiMat	blood
3	chr8:115335000-115338600	Weak transcription	Hela-S3	cervix
4	chr8:115336000-115336800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr8:115341600-115342000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr8:115349600-115350200	Enhancers	Fetal Lung	lung
7	chr8:115350200-115355400	Weak transcription	Fetal Lung	lung
8	chr8:115354400-115355800	Active TSS	Brain Anterior Caudate	brain
9	chr8:115355400-115355600	Enhancers	Fetal Lung	lung
10	chr8:115370200-115371200	Enhancers	Adipose Nuclei	Adipose
11	chr8:115370800-115371200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr8:115370800-115371400	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr8:115372800-115373400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr8:115381200-115382600	Enhancers	Hela-S3	cervix
15	chr8:115385400-115385600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr8:115395200-115396000	Enhancers	H9 Cell Line	embryonic stem cell
17	chr8:115395600-115396000	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr8:115395800-115396200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr8:115397400-115397600	Enhancers	Fetal Lung	lung
20	chr8:115399000-115399200	Enhancers	Hela-S3	cervix
21	chr8:115399200-115399600	Flanking Active TSS	Hela-S3	cervix
22	chr8:115399600-115399800	Weak transcription	Fetal Lung	lung
23	chr8:115399600-115400600	Active TSS	Hela-S3	cervix
24	chr8:115399800-115400800	Enhancers	Fetal Lung	lung
25	chr8:115400600-115400800	Flanking Active TSS	Hela-S3	cervix
26	chr8:115400800-115402200	Enhancers	Hela-S3	cervix
27	chr8:115431600-115432200	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr8:115435200-115436000	Enhancers	Hela-S3	cervix
29	chr8:115437400-115437800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr8:115437400-115438000	Enhancers	Dnd41	blood
31	chr8:115446800-115447600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr8:115447600-115448000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr8:115447600-115449000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr8:115448000-115449000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr8:115448000-115461800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr8:115448400-115448800	Active TSS	GM12878-XiMat	blood
37	chr8:115448800-115450600	Weak transcription	GM12878-XiMat	blood
38	chr8:115450600-115451000	Enhancers	GM12878-XiMat	blood
39	chr8:115454600-115455200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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