Variant report

Variant	nsv968544
Chromosome Location	chr8:48092599-48101564
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:138)
CpG islands
(count:734)
Chromatin interactive
region (count:7)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:138 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CCNT2	chr8:48100257-48100420	K562	blood:	n/a	n/a
2	CEBPB	chr8:48096843-48096859	K562	blood:	n/a	n/a
3	CEBPB	chr8:48095552-48095745	K562	blood:	n/a	n/a
4	CTCF	chr8:48100580-48100730	GM12869	blood:	n/a	n/a
5	CTCF	chr8:48100540-48100690	SAEC	small airway:	n/a	n/a
6	CTCF	chr8:48100220-48100370	SK-N-SH_RA	brain:	n/a	n/a
7	CTCF	chr8:48100240-48100390	AoAF	blood vessel:	n/a	n/a
8	CTCF	chr8:48100900-48101050	HRE	kidney:	n/a	n/a
9	CTCF	chr8:48100960-48101110	HUVEC	blood vessel:	n/a	n/a
10	CTCF	chr8:48100480-48100630	BJ	skin:	n/a	n/a
11	CTCF	chr8:48100100-48100250	HRE	kidney:	n/a	n/a
12	CTCF	chr8:48100448-48100600	MCF-7	breast:	n/a	n/a
13	CTCF	chr8:48100160-48100310	HCFaa	heart:	n/a	n/a
14	CTCF	chr8:48100080-48100230	AG10803	skin:	n/a	n/a
15	CTCF	chr8:48100480-48100630	BE2_C	brain:	n/a	n/a
16	CTCF	chr8:48100200-48100350	BJ	skin:	n/a	n/a
17	CTCF	chr8:48100100-48100250	HBMEC	blood vessel:	n/a	n/a
18	CTCF	chr8:48095920-48096070	GM12873	blood:	n/a	n/a
19	CTCF	chr8:48100200-48100350	HCPEpiC	choroid plexus:	n/a	n/a
20	CTCF	chr8:48100123-48100398	MCF-7	breast:	n/a	n/a
21	CTCF	chr8:48100780-48100930	BJ	skin:	n/a	n/a
22	CTCF	chr8:48100540-48100690	GM12865	blood:	n/a	n/a
23	CTCF	chr8:48100420-48100570	MCF-7	breast:	n/a	n/a
24	CTCF	chr8:48100980-48101130	AG10803	skin:	n/a	n/a
25	CTCF	chr8:48100154-48100291	Spleen_OC	spleen:	n/a	n/a
26	CTCF	chr8:48100500-48100650	GM12868	blood:	n/a	n/a
27	CTCF	chr8:48100080-48100230	HAc	cerebellar:	n/a	n/a
28	CTCF	chr8:48100540-48100690	HUVEC	blood vessel:	n/a	n/a
29	CTCF	chr8:48100160-48100310	MCF-7	breast:	n/a	n/a
30	CTCF	chr8:48100500-48100650	GM12873	blood:	n/a	n/a
31	CTCF	chr8:48100871-48101016	MCF-7	breast:	n/a	n/a
32	CTCF	chr8:48100840-48100990	GM12873	blood:	n/a	n/a
33	CTCF	chr8:48100892-48100960	MCF-7	breast:	n/a	n/a
34	CTCF	chr8:48100460-48100610	HepG2	liver:	n/a	n/a
35	CTCF	chr8:48100197-48100273	NHEK	skin:	n/a	n/a
36	CTCF	chr8:48100480-48100630	HMEC	breast:	n/a	n/a
37	CTCF	chr8:48100461-48100486	LNCaP	prostate:	n/a	n/a
38	CTCF	chr8:48100871-48100999	MCF-7	breast:	n/a	n/a
39	CTCF	chr8:48100720-48100870	BJ	skin:	n/a	n/a
40	CTCF	chr8:48100391-48100452	LNCaP	prostate:	n/a	n/a
41	CTCF	chr8:48100154-48100346	Fibrobl	skin:	n/a	n/a
42	CTCF	chr8:48100180-48100330	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr8:48100320-48100470	AG09309	skin:	n/a	n/a
44	CTCF	chr8:48100460-48100610	AG10803	skin:	n/a	n/a
45	CTCF	chr8:48100140-48100290	HCM	heart:	n/a	n/a
46	CTCF	chr8:48100180-48100330	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr8:48100144-48100343	MCF-7	breast:	n/a	n/a
48	CTCF	chr8:48100360-48100610	GM12873	blood:	n/a	n/a
49	CTCF	chr8:48100460-48100625	MCF-7	breast:	n/a	n/a
50	CTCF	chr8:48100500-48100650	A549	lung:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:48100170-48100220	HAEpiC	amniotic membrane:	n/a
2	chr8:48100957-48101007	BJ	skin:	n/a
3	chr8:48100170-48100220	HAEpiC	amniotic membrane:	n/a
4	chr8:48100957-48101007	BJ	skin:	n/a
5	chr8:48097610-48097660	HUVEC	blood vessel:	n/a
6	chr8:48100429-48100479	HL-60	blood:	n/a
7	chr8:48100957-48101007	PANC-1	pancreas:	n/a
8	chr8:48100081-48100131	NH-A	brain:	n/a
9	chr8:48100908-48100958	GM12878	blood:	n/a
10	chr8:48100898-48100948	LNCaP	prostate:	n/a
11	chr8:48100186-48100236	IMR90	lung:	fetal
12	chr8:48097610-48097660	SK-N-SH	brain:	n/a
13	chr8:48100186-48100236	LNCaP	prostate:	n/a
14	chr8:48100898-48100948	ovcar-3	ovarian:	n/a
15	chr8:48099615-48099665	ProgFib	skin:	n/a
16	chr8:48099615-48099665	GM19239	blood:	n/a
17	chr8:48099615-48099665	HRPEpiC	eye:	n/a
18	chr8:48100186-48100236	HepG2	liver:	n/a
19	chr8:48100868-48100918	HepG2	liver:	n/a
20	chr8:48100170-48100220	GM12878	blood:	n/a
21	chr8:48100186-48100236	GM06990	blood:	n/a
22	chr8:48100957-48101007	HMEC	breast:	n/a
23	chr8:48100898-48100948	NT2-D1	testis:	n/a
24	chr8:48100429-48100479	SKMC	muscle:	n/a
25	chr8:48100410-48100460	IMR90	lung:	fetal
26	chr8:48100179-48100229	Hepatocyte	liver:	n/a
27	chr8:48100410-48100460	SAEC	small airway:	n/a
28	chr8:48100186-48100236	CMK	blood:	n/a
29	chr8:48100898-48100948	MCF10A-Er-Src	breast:	n/a
30	chr8:48100957-48101007	ECC-1	luminal epithelium:	n/a
31	chr8:48100898-48100948	HUVEC	blood vessel:	n/a
32	chr8:48100186-48100236	HIPEpiC	eye:	n/a
33	chr8:48099615-48099665	BJ	skin:	n/a
34	chr8:48100186-48100236	PANC-1	pancreas:	n/a
35	chr8:48100868-48100918	U87	brain:	n/a
36	chr8:48100179-48100229	GM06990	blood:	n/a
37	chr8:48100868-48100918	AoSMC	blood vessel:	n/a
38	chr8:48100429-48100479	HMEC	breast:	n/a
39	chr8:48100868-48100918	HMEC	breast:	n/a
40	chr8:48100410-48100460	GM12892	blood:	n/a
41	chr8:48100957-48101007	HRCEpiC	kidney:	n/a
42	chr8:48100957-48101007	HRE	kidney:	n/a
43	chr8:48100081-48100131	BJ	skin:	n/a
44	chr8:48100868-48100918	Hepatocyte	liver:	n/a
45	chr8:48097610-48097660	Jurkat	blood:	n/a
46	chr8:48100170-48100220	NH-A	brain:	n/a
47	chr8:48100908-48100958	GM12892	blood:	n/a
48	chr8:48100429-48100479	NT2-D1	testis:	n/a
49	chr8:48097610-48097660	HEK293	kidney:	embryo
50	chr8:48097610-48097660	Caco-2	colon:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:48090533..48093121-chr8:48649815..48651920,2	MCF-7	breast:
2	chr8:48090559..48092887-chr8:48171914..48174846,2	MCF-7	breast:
3	chr8:48091200..48093897-chr8:48104866..48107848,2	K562	blood:
4	chr8:48089038..48091327-chr8:48097909..48100771,2	MCF-7	breast:
5	chr8:48094665..48096718-chr8:48111922..48113998,2	MCF-7	breast:
6	chr8:47868480..47869132-chr8:48100099..48100692,2	MCF-7	breast:
7	chr8:48078768..48081017-chr8:48097820..48099416,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-1134I14.8.1-1	chr8:48100930-48104439	NONHSAT126435
2	lnc-RP11-1134I14.8.1-1	chr8:48100928-48101183	NONHSAT126434
3	lnc-RP11-1134I14.8.1-1	chr8:48101531-48101575	NONHSAT126436

No data

Variant related genes	Relation type
ENSG00000254348	TF binding region
ENSG00000255366	TF binding region
ENSG00000254348	CpG island
ENSG00000255366	CpG island
ENSG00000253502	chromatin interactions
ENSG00000164808	chromatin interactions
ENSG00000221869	chromatin interactions

Extended variants
information (count: 335 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:335 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565409381	chr8:48092615-48092616	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs532487136	chr8:48092654-48092655	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs551200808	chr8:48092655-48092656	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs540328508	chr8:48092699-48092700	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs369808960	chr8:48092700-48092701	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs569425181	chr8:48092782-48092783	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs190289587	chr8:48092785-48092786	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs181641820	chr8:48092798-48092799	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs75821046	chr8:48092814-48092815	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs534641377	chr8:48092886-48092887	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs552678332	chr8:48092888-48092889	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs571359483	chr8:48092915-48092916	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs532603647	chr8:48092918-48092919	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs538353710	chr8:48093011-48093012	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs370290222	chr8:48093034-48093035	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs552768358	chr8:48093061-48093062	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs556741610	chr8:48093062-48093063	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs575056521	chr8:48093122-48093123	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs144974099	chr8:48093137-48093138	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs554418950	chr8:48093141-48093142	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs116205863	chr8:48093175-48093176	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs540660384	chr8:48093190-48093191	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs563053364	chr8:48093200-48093201	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs565130973	chr8:48093231-48093232	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs577268551	chr8:48093330-48093331	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs148662642	chr8:48093416-48093417	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs72644571	chr8:48093431-48093432	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs4872962	chr8:48093483-48093484	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs77208117	chr8:48093523-48093524	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs185718701	chr8:48093529-48093530	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs78272699	chr8:48093674-48093675	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs556281662	chr8:48093721-48093722	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs567199447	chr8:48093753-48093754	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs546622872	chr8:48093763-48093764	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs142443886	chr8:48093800-48093801	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs377757856	chr8:48093895-48093896	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs536198337	chr8:48093908-48093909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs571110588	chr8:48093918-48093919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538739038	chr8:48093933-48093934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs73581087	chr8:48093948-48093949	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs543408878	chr8:48093964-48093965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs377367299	chr8:48093965-48093966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190190282	chr8:48093982-48093983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs536073122	chr8:48094018-48094019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs182372728	chr8:48094021-48094022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs573135907	chr8:48094047-48094048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185989363	chr8:48094113-48094114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538480463	chr8:48094148-48094149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577128939	chr8:48094199-48094200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544713538	chr8:48094202-48094203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
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
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	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
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medulloblastoma	20607354	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
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	20409316	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
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Tetralogy of Fallot	22912587	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	22522925	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD

Chromatin state (count:250 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:48091600-48093000	Weak transcription	Right Atrium	heart
2	chr8:48092000-48100000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr8:48093400-48093600	Enhancers	Right Atrium	heart
4	chr8:48095000-48097000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr8:48098800-48099400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
6	chr8:48099000-48099400	Enhancers	Brain Cingulate Gyrus	brain
7	chr8:48099000-48099600	Enhancers	Fetal Brain Male	brain
8	chr8:48099200-48099400	Enhancers	Aorta	Aorta
9	chr8:48099200-48099400	Enhancers	Brain Inferior Temporal Lobe	brain
10	chr8:48099200-48099600	Enhancers	Brain Angular Gyrus	brain
11	chr8:48099200-48099600	Enhancers	Brain Hippocampus Middle	brain
12	chr8:48099200-48101200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr8:48099400-48099600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr8:48099400-48099600	Flanking Active TSS	Brain Cingulate Gyrus	brain
15	chr8:48099400-48099600	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
16	chr8:48099400-48099600	Enhancers	Fetal Brain Female	brain
17	chr8:48099400-48099600	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
18	chr8:48099400-48099600	Enhancers	Spleen	Spleen
19	chr8:48099400-48099800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
20	chr8:48099400-48100000	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr8:48099400-48100000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
22	chr8:48099400-48100000	Bivalent Enhancer	Fetal Stomach	stomach
23	chr8:48099400-48100600	Active TSS	Pancreas	Pancrea
24	chr8:48099600-48099800	Flanking Active TSS	Brain Angular Gyrus	brain
25	chr8:48099600-48099800	Enhancers	Brain Cingulate Gyrus	brain
26	chr8:48099600-48099800	Flanking Active TSS	Brain Hippocampus Middle	brain
27	chr8:48099600-48099800	Flanking Active TSS	Fetal Brain Female	brain
28	chr8:48099600-48100000	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr8:48099600-48100000	Enhancers	Brain Substantia Nigra	brain
30	chr8:48099600-48100000	Enhancers	Colon Smooth Muscle	Colon
31	chr8:48099600-48100000	Bivalent Enhancer	Duodenum Mucosa	Duodenum
32	chr8:48099600-48100000	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
33	chr8:48099600-48100200	Flanking Active TSS	Fetal Brain Male	brain
34	chr8:48099600-48100200	Bivalent/Poised TSS	Skeletal Muscle Female	skeletal muscle
35	chr8:48099600-48100200	Weak transcription	Spleen	Spleen
36	chr8:48099600-48100600	Active TSS	Stomach Smooth Muscle	stomach
37	chr8:48099600-48101000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr8:48099600-48101000	Active TSS	Brain Anterior Caudate	brain
39	chr8:48099600-48101400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
40	chr8:48099800-48101000	Active TSS	Brain Hippocampus Middle	brain
41	chr8:48099800-48101200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr8:48099800-48101400	Active TSS	Brain Cingulate Gyrus	brain
43	chr8:48099800-48101400	Active TSS	Brain Inferior Temporal Lobe	brain
44	chr8:48099800-48101800	Active TSS	Brain Angular Gyrus	brain
45	chr8:48099800-48102000	Active TSS	Fetal Brain Female	brain
46	chr8:48100000-48100200	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr8:48100000-48100200	Bivalent/Poised TSS	Primary B cells from cord blood	blood
48	chr8:48100000-48100200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
49	chr8:48100000-48100200	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
50	chr8:48100000-48100200	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood

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