Variant report

Variant	nsv972564
Chromosome Location	chr8:103448714-103461127
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr8:103448493-103448823	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr8:103459025-103459378	HepG2	liver:	n/a	chr8:103459195-103459204 chr8:103459195-103459206 chr8:103459193-103459204
3	CEBPB	chr8:103459129-103459282	HepG2	liver:	n/a	chr8:103459195-103459204 chr8:103459195-103459206 chr8:103459193-103459204
4	CEBPB	chr8:103456507-103456791	K562	blood:	n/a	chr8:103456653-103456664
5	CEBPB	chr8:103459138-103459332	A549	lung:	n/a	chr8:103459195-103459204 chr8:103459195-103459206 chr8:103459193-103459204
6	CEBPB	chr8:103456528-103456757	K562	blood:	n/a	chr8:103456653-103456664
7	CEBPB	chr8:103456501-103456812	HepG2	liver:	n/a	chr8:103456653-103456664
8	CEBPB	chr8:103459051-103459333	K562	blood:	n/a	chr8:103459195-103459204 chr8:103459195-103459206 chr8:103459193-103459204
9	CTCF	chr8:103449080-103449230	AoAF	blood vessel:	n/a	chr8:103449131-103449139
10	CTCF	chr8:103449140-103449290	A549	lung:	n/a	n/a
11	CTCF	chr8:103449104-103449286	Hela-S3	cervix:	n/a	chr8:103449131-103449139
12	CTCF	chr8:103449080-103449230	HBMEC	blood vessel:	n/a	chr8:103449131-103449139
13	CTCF	chr8:103449140-103449290	AG09309	skin:	n/a	n/a
14	CTCF	chr8:103456982-103456985	GM10266	blood:	n/a	n/a
15	CTCF	chr8:103449140-103449290	HMF	breast:	n/a	n/a
16	CTCF	chr8:103449120-103449270	HRPEpiC	eye:	n/a	chr8:103449131-103449139
17	CTCF	chr8:103449120-103449270	HepG2	liver:	n/a	chr8:103449131-103449139
18	CTCF	chr8:103449100-103449250	HCPEpiC	choroid plexus:	n/a	chr8:103449131-103449139
19	CTCF	chr8:103449180-103449330	RPTEC	kidney:	n/a	n/a
20	CTCF	chr8:103449060-103449210	HCM	heart:	n/a	chr8:103449131-103449139
21	CTCF	chr8:103449140-103449290	Caco-2	colon:	n/a	n/a
22	CTCF	chr8:103449109-103449287	MCF-7	breast:	n/a	chr8:103449131-103449139
23	CTCF	chr8:103449100-103449250	HPAF	blood vessel:	n/a	chr8:103449131-103449139
24	CTCF	chr8:103449220-103449370	RPTEC	kidney:	n/a	n/a
25	CTCF	chr8:103449156-103449262	Pancreas_OC	pancreas:	n/a	n/a
26	CTCF	chr8:103449084-103449309	HepG2	liver:	n/a	chr8:103449131-103449139
27	CTCF	chr8:103449120-103449270	HA-sp	spinal cord:	n/a	chr8:103449131-103449139
28	CTCF	chr8:103449179-103449237	NHEK	skin:	n/a	n/a
29	CTCF	chr8:103449019-103449365	MCF-7	breast:	n/a	chr8:103449131-103449139
30	CTCF	chr8:103449160-103449310	HEEpiC	esophagus:	n/a	n/a
31	CTCF	chr8:103449100-103449250	AG04449	skin:	n/a	chr8:103449131-103449139
32	CTCF	chr8:103454390-103454420	Lung_OC	lung:	n/a	n/a
33	CTCF	chr8:103449180-103449330	HPF	lung:	n/a	n/a
34	CTCF	chr8:103456953-103456978	GM10266	blood:	n/a	n/a
35	CTCF	chr8:103449120-103449270	AG09319	gingival:	n/a	chr8:103449131-103449139
36	CTCF	chr8:103449100-103449250	MCF-7	breast:	n/a	chr8:103449131-103449139
37	CTCF	chr8:103449140-103449290	AG04450	lung:	n/a	n/a
38	CTCF	chr8:103449160-103449211	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr8:103449075-103449279	HepG2	liver:	n/a	chr8:103449131-103449139
40	CTCF	chr8:103449087-103449318	IMR90	lung:	n/a	chr8:103449131-103449139
41	CTCF	chr8:103449100-103449250	HMEC	breast:	n/a	chr8:103449131-103449139
42	CTCF	chr8:103449052-103449327	H1-hESC	embryonic stem cell:	n/a	chr8:103449131-103449139
43	CTCF	chr8:103449160-103449310	MCF-7	breast:	n/a	n/a
44	CTCF	chr8:103449080-103449230	HPF	lung:	n/a	chr8:103449131-103449139
45	CTCF	chr8:103449120-103449270	HPAF	blood vessel:	n/a	chr8:103449131-103449139
46	CTCF	chr8:103449160-103449310	AG09319	gingival:	n/a	n/a
47	CTCF	chr8:103449120-103449270	HVMF	connective:	n/a	chr8:103449131-103449139
48	CTCF	chr8:103449086-103449315	T-47D	breast:	n/a	chr8:103449131-103449139
49	CTCF	chr8:103449120-103449270	AG09309	skin:	n/a	chr8:103449131-103449139
50	CTCF	chr8:103449120-103449270	HCPEpiC	choroid plexus:	n/a	chr8:103449131-103449139

No.	Distal block	Cell Line	Cell type
1	chr8:103421569..103424868-chr8:103447011..103449629,3	MCF-7	breast:
2	chr8:103439421..103441100-chr8:103448054..103450571,2	MCF-7	breast:
3	chr8:103446967..103449088-chr8:103820705..103822908,2	MCF-7	breast:
4	chr8:103448154..103449973-chr8:103656128..103658488,2	MCF-7	breast:
5	chr17:57919324..57922033-chr8:103458324..103460694,2	MCF-7	breast:
6	chr8:103448723..103449619-chr8:103540793..103541456,2	MCF-7	breast:
7	chr8:103436437..103439478-chr8:103450415..103454144,3	MCF-7	breast:
8	chr8:103432099..103434551-chr8:103448773..103451141,2	MCF-7	breast:
9	chr8:103423291..103426053-chr8:103446476..103449606,3	MCF-7	breast:
10	chr8:103422125..103426655-chr8:103454292..103458691,6	MCF-7	breast:

Variant related genes	Relation type
HSPE1P14	TF binding region
ENSG00000253633	chromatin interactions
ENSG00000221387	chromatin interactions
ENSG00000104517	chromatin interactions

Extended variants
information (count: 375 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:375 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116916308	chr8:103448717-103448718	Flanking Active TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs147476575	chr8:103448718-103448719	Flanking Active TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs138371667	chr8:103448743-103448744	Flanking Active TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs368125872	chr8:103448795-103448796	Flanking Active TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs540613872	chr8:103448827-103448828	Flanking Active TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs143930193	chr8:103448834-103448835	Flanking Active TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs530802745	chr8:103448883-103448884	Flanking Active TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs542967176	chr8:103448951-103448952	Flanking Active TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs561128547	chr8:103448959-103448960	Flanking Active TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs528536444	chr8:103449047-103449048	Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs546703201	chr8:103449066-103449067	Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs565521219	chr8:103449068-103449069	Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs117987110	chr8:103449074-103449075	Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs371852557	chr8:103449121-103449122	Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs551380406	chr8:103449131-103449132	Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs369346184	chr8:103449157-103449158	Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs528746005	chr8:103449163-103449164	Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs536951747	chr8:103449182-103449183	Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs186859766	chr8:103449198-103449199	Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs567288052	chr8:103449204-103449205	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs534692200	chr8:103449228-103449229	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs72683010	chr8:103449343-103449344	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs192216732	chr8:103449352-103449353	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs537405295	chr8:103449375-103449376	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs11465170	chr8:103449376-103449377	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs397812370	chr8:103449382-103449383	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs201606719	chr8:103449383-103449384	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs557184118	chr8:103449414-103449415	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs200509455	chr8:103449472-103449473	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs184999158	chr8:103449473-103449474	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs62523143	chr8:103449477-103449478	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs189508818	chr8:103449489-103449490	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs61317409	chr8:103449500-103449501	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs376593135	chr8:103449575-103449576	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs369019330	chr8:103449616-103449617	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs528498723	chr8:103449620-103449621	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs540306260	chr8:103449642-103449643	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs565081219	chr8:103449723-103449724	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs532949405	chr8:103449783-103449784	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs139415069	chr8:103449793-103449794	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs6984894	chr8:103449800-103449801	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs59718958	chr8:103449817-103449818	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs569775386	chr8:103449846-103449847	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs113720965	chr8:103449862-103449863	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs182166106	chr8:103449873-103449874	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs567249494	chr8:103449908-103449909	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs571810324	chr8:103449985-103449986	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs116696394	chr8:103450001-103450002	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs572402696	chr8:103450026-103450027	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs148467013	chr8:103450054-103450055	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:121)

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
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
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
Multiple myeloma	16461302	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
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
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	17260012	CNVD
Sezary syndrome	18413736	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Cancer	20164920	CNVD
Urothelial cell carcinoma	18451213	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	16912164	CNVD
Breast cancer	20409316	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21611746	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Autism	22495309	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:65 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:103438600-103449200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr8:103447000-103448800	Enhancers	H9 Cell Line	embryonic stem cell
3	chr8:103447000-103449800	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr8:103447000-103449800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr8:103447200-103450800	Enhancers	H1 Cell Line	embryonic stem cell
6	chr8:103447400-103449400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr8:103447400-103449600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr8:103448400-103449000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr8:103448400-103449000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
10	chr8:103448400-103453400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr8:103448600-103449000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
12	chr8:103448600-103449000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
13	chr8:103448600-103449000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
14	chr8:103448600-103449200	Active TSS	iPS-20b Cell Line	embryonic stem cell
15	chr8:103448600-103449400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr8:103448800-103449600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr8:103448800-103449600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr8:103448800-103450400	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr8:103449000-103449200	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr8:103449000-103449200	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr8:103449000-103449200	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr8:103449000-103449200	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr8:103449000-103449400	Active TSS	ES-I3 Cell Line	embryonic stem cell
24	chr8:103449200-103449400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
25	chr8:103449200-103449600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
26	chr8:103449200-103449600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
27	chr8:103449200-103449600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
28	chr8:103449200-103449600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
29	chr8:103449200-103449600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr8:103449400-103449600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
31	chr8:103449400-103449600	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr8:103449400-103449800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
33	chr8:103449600-103449800	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr8:103449600-103449800	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr8:103449600-103450000	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr8:103449600-103450600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr8:103449600-103450800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr8:103449600-103451000	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr8:103449600-103453000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr8:103449600-103453000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr8:103449800-103450800	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr8:103449800-103450800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr8:103449800-103453200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr8:103450000-103450400	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr8:103450400-103451200	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr8:103450600-103450800	Enhancers	H9 Cell Line	embryonic stem cell
47	chr8:103450600-103451200	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr8:103450800-103451000	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr8:103450800-103451200	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr8:103450800-103451200	Enhancers	HUES64 Cell Line	embryonic stem cell

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