Variant report

Variant	nsv1054286
Chromosome Location	chr13:88023520-88206587
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:274)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:274 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr13:88082864-88082918	K562	blood:	n/a	n/a
2	BCL11A	chr13:88188747-88189098	GM12878	blood:	n/a	n/a
3	BHLHE40	chr13:88096440-88096715	GM12878	blood:	n/a	n/a
4	BHLHE40	chr13:88206384-88206692	GM12878	blood:	n/a	n/a
5	BHLHE40	chr13:88188832-88189566	GM12878	blood:	n/a	n/a
6	CEBPB	chr13:88094207-88094561	HepG2	liver:	n/a	chr13:88094372-88094383
7	CEBPB	chr13:88078861-88079143	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr13:88094236-88094497	K562	blood:	n/a	chr13:88094372-88094383
9	CEBPB	chr13:88166206-88166451	HepG2	liver:	n/a	chr13:88166294-88166307 chr13:88166294-88166305 chr13:88166296-88166307
10	CEBPB	chr13:88107751-88107960	HepG2	liver:	n/a	chr13:88107869-88107880
11	CHD1	chr13:88189433-88189865	GM12878	blood:	n/a	n/a
12	CHD2	chr13:88188672-88189531	GM12878	blood:	n/a	n/a
13	CTCF	chr13:88048420-88048570	GM12867	blood:	n/a	n/a
14	CTCF	chr13:88050400-88050550	WERI-Rb-1	eye:	n/a	n/a
15	CTCF	chr13:88175315-88175321	GM20000	blood:	n/a	n/a
16	CTCF	chr13:88112920-88113070	GM06990	blood:	n/a	n/a
17	CTCF	chr13:88057280-88057430	RPTEC	kidney:	n/a	n/a
18	CTCF	chr13:88185397-88185429	GM10266	blood:	n/a	n/a
19	CTCF	chr13:88175290-88175308	GM20000	blood:	n/a	n/a
20	CTCF	chr13:88050400-88050550	HAc	cerebellar:	n/a	n/a
21	CTCF	chr13:88050469-88050532	Medullo	brain:	n/a	n/a
22	CTCF	chr13:88050408-88050589	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr13:88193756-88193819	ProgFib	skin:	n/a	n/a
24	CTCF	chr13:88033720-88033870	NB4	blood:	n/a	n/a
25	CTCF	chr13:88057250-88057450	GM12878	blood:	n/a	n/a
26	CTCF	chr13:88050482-88050517	HepG2	liver:	n/a	n/a
27	CTCF	chr13:88151800-88151950	GM06990	blood:	n/a	n/a
28	CTCF	chr13:88050360-88050510	RPTEC	kidney:	n/a	n/a
29	CTCF	chr13:88050356-88050608	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr13:88194472-88194509	ProgFib	skin:	n/a	n/a
31	CTCF	chr13:88050456-88050519	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr13:88050400-88050550	RPTEC	kidney:	n/a	n/a
33	CTCF	chr13:88195238-88195309	GM20000	blood:	n/a	n/a
34	CTCF	chr13:88050460-88050610	HBMEC	blood vessel:	n/a	n/a
35	CUX1	chr13:88188804-88188985	GM12878	blood:	n/a	n/a
36	CUX1	chr13:88177242-88177433	GM12878	blood:	n/a	n/a
37	E2F4	chr13:88151541-88151638	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr13:88092929-88093361	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F4	chr13:88127724-88128291	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr13:88060491-88060691	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr13:88107539-88107633	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr13:88195921-88195989	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr13:88125345-88125541	MCF10A-Er-Src	breast:	n/a	n/a
44	EBF1	chr13:88172514-88172885	GM12878	blood:	n/a	chr13:88172667-88172678
45	EBF1	chr13:88188325-88189595	GM12878	blood:	n/a	n/a
46	EBF1	chr13:88096403-88096631	GM12878	blood:	n/a	n/a
47	EBF1	chr13:88205072-88205665	GM12878	blood:	n/a	n/a
48	EBF1	chr13:88206262-88206574	GM12878	blood:	n/a	n/a
49	EBF1	chr13:88190801-88191001	GM12878	blood:	n/a	n/a
50	EBF1	chr13:88174345-88174847	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:88078884-88078934	HEEpiC	esophagus:	n/a
2	chr13:88078884-88078934	H1-hESC	embryonic stem cell:	embryo
3	chr13:88078884-88078934	MCF10A-Er-Src	breast:	n/a
4	chr13:88078884-88078934	NT2-D1	testis:	n/a
5	chr13:88078884-88078934	AG04450	lung:	fetal
6	chr13:88078884-88078934	GM19239	blood:	n/a
7	chr13:88078884-88078934	HL-60	blood:	n/a
8	chr13:88078884-88078934	HUVEC	blood vessel:	n/a
9	chr13:88078884-88078934	HPAEpiC	pulmonary alveolar:	n/a
10	chr13:88078884-88078934	HAEpiC	amniotic membrane:	n/a
11	chr13:88078884-88078934	HMEC	breast:	n/a
12	chr13:88078884-88078934	GM06990	blood:	n/a
13	chr13:88078884-88078934	ProgFib	skin:	n/a
14	chr13:88078884-88078934	PFSK-1	brain:	n/a
15	chr13:88078884-88078934	HRE	kidney:	n/a
16	chr13:88078884-88078934	U87	brain:	n/a
17	chr13:88078884-88078934	AG10803	skin:	n/a
18	chr13:88078884-88078934	AG09319	gingival:	n/a
19	chr13:88078884-88078934	AG04449	skin:	fetal
20	chr13:88078884-88078934	SK-N-MC	brain:	n/a
21	chr13:88078884-88078934	HCPEpiC	choroid plexus:	n/a
22	chr13:88078884-88078934	SKMC	muscle:	n/a
23	chr13:88078884-88078934	ovcar-3	ovarian:	n/a
24	chr13:88078884-88078934	GM12891	blood:	n/a
25	chr13:88078884-88078934	HCF	heart:	n/a
26	chr13:88078884-88078934	Hela-S3	cervix:	n/a
27	chr13:88078884-88078934	BE2_C	brain:	n/a
28	chr13:88078884-88078934	HCM	heart:	n/a
29	chr13:88078884-88078934	PrEC	prostate:	n/a
30	chr13:88078884-88078934	PANC-1	pancreas:	n/a
31	chr13:88078884-88078934	IMR90	lung:	fetal
32	chr13:88078884-88078934	NHBE	bronchial:	n/a
33	chr13:88078884-88078934	HEK293	kidney:	embryo
34	chr13:88078884-88078934	Jurkat	blood:	n/a
35	chr13:88078884-88078934	A549	lung:	n/a
36	chr13:88078884-88078934	HRPEpiC	eye:	n/a
37	chr13:88078884-88078934	LNCaP	prostate:	n/a
38	chr13:88078884-88078934	AoSMC	blood vessel:	n/a
39	chr13:88078884-88078934	Hepatocyte	liver:	n/a
40	chr13:88078884-88078934	GM12892	blood:	n/a
41	chr13:88078884-88078934	GM12878	blood:	n/a
42	chr13:88078884-88078934	NH-A	brain:	n/a
43	chr13:88078884-88078934	HRCEpiC	kidney:	n/a
44	chr13:88078884-88078934	T-47D	breast:	n/a
45	chr13:88078884-88078934	HIPEpiC	eye:	n/a
46	chr13:88078884-88078934	SK-N-SH_RA	brain:	n/a
47	chr13:88078884-88078934	ECC-1	luminal epithelium:	n/a
48	chr13:88078884-88078934	CMK	blood:	n/a
49	chr13:88078884-88078934	HepG2	liver:	n/a
50	chr13:88078884-88078934	NB4	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:88107156..88107790-chr5:66024900..66025639,2	MCF-7	breast:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK6-9	chr13:88125695-88125808	ENSG00000228824
2	lnc-SLITRK6-9	chr13:88113179-88113224	XLOC_010683
3	lnc-SLITRK6-9	chr13:88099351-88099488	XLOC_010683
4	lnc-SLITRK6-9	chr13:88080353-88080410	ENSG00000228824.2
5	lnc-SLITRK6-9	chr13:88099351-88099488	ENSG00000228824.2
6	lnc-SLITRK6-9	chr13:88099351-88099490	ENSG00000232636.2
7	lnc-SLITRK6-9	chr13:88099351-88099488	ENSG00000228824
8	lnc-SLITRK6-9	chr13:88096247-88097385	ENSG00000228824
9	lnc-SLITRK6-9	chr13:88163621-88163725	XLOC_010683
10	lnc-SLITRK6-8	chr13:88079469-88079802	XLOC_010682
11	lnc-SLITRK6-8	chr13:88080353-88080528	XLOC_010682
12	lnc-SLITRK6-9	chr13:88096242-88097385	XLOC_010683
13	lnc-SLITRK6-9	chr13:88113179-88113224	ENSG00000228824
14	lnc-SLITRK6-9	chr13:88079469-88079802	ENSG00000228824.2
15	lnc-SLITRK6-9	chr13:88079455-88079802	ENSG00000232636.2
16	lnc-SLITRK6-9	chr13:88125695-88125808	XLOC_010683
17	lnc-SLITRK6-9	chr13:88113179-88113224	ENSG00000228824.2
18	lnc-SLITRK6-9	chr13:88097266-88097385	ENSG00000232636.2
19	lnc-SLITRK6-9	chr13:88163621-88163725	ENSG00000228824
20	lnc-SLITRK6-9	chr13:88080353-88080410	ENSG00000232636.2

No data

Variant related genes	Relation type
ENSG00000232636	TF binding region
MIR4500HG	TF binding region
LIN28AP2	TF binding region
ENSG00000232636	CpG island
MIR4500HG	CpG island
LIN28AP2	CpG island
WARS2	miRNA target sites
SCD	miRNA target sites
MIB1	miRNA target sites
DPF2	miRNA target sites
DENR	miRNA target sites

Extended variants
information (count: 1394 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1394 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9556712	chr13:88023525-88023526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs527944505	chr13:88023526-88023527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148922709	chr13:88023540-88023541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs184411518	chr13:88023592-88023593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370328597	chr13:88023615-88023616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs114192107	chr13:88023620-88023621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs116309359	chr13:88023624-88023625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs568570440	chr13:88023642-88023643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs189410554	chr13:88023655-88023656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs535600242	chr13:88023680-88023681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs200191222	chr13:88023769-88023770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs554103039	chr13:88023770-88023771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs113706591	chr13:88023781-88023782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184532272	chr13:88023791-88023792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558937844	chr13:88023819-88023820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577099913	chr13:88023859-88023860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555125578	chr13:88023878-88023879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs189239363	chr13:88023880-88023881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs555963745	chr13:88023890-88023891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181764609	chr13:88023891-88023892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs541574965	chr13:88023904-88023905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs560053674	chr13:88023950-88023951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534304630	chr13:88023974-88023975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs543982643	chr13:88023977-88023978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs560897847	chr13:88023994-88023995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs143680686	chr13:88023995-88023996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559053720	chr13:88024027-88024028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs577314550	chr13:88024091-88024092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs148110355	chr13:88024128-88024129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs141302171	chr13:88024130-88024131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs9516921	chr13:88024152-88024153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs540255782	chr13:88024158-88024159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373619268	chr13:88024167-88024168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562161235	chr13:88024169-88024170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs73563790	chr13:88024183-88024184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547580866	chr13:88024200-88024201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs115024458	chr13:88024201-88024202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs115662789	chr13:88024226-88024227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186324619	chr13:88024244-88024245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs570785895	chr13:88024275-88024276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs9584568	chr13:88024289-88024290	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs138973978	chr13:88024325-88024326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs574555549	chr13:88024326-88024327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs367753202	chr13:88024379-88024380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs75734166	chr13:88024396-88024397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371504192	chr13:88024413-88024414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189660677	chr13:88024547-88024548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs180725039	chr13:88024563-88024564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs137873683	chr13:88024605-88024606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs202223737	chr13:88024677-88024678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
abnormal development	18461090	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Cancer	21220470	CNVD
Cancer	21183584	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Mantle cell lymphoma	19690137	CNVD
Rhabdomyosarcoma	17210683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Breast cancer	17142309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Mental retardation	17847001	CNVD
Medulloblastoma	19270706	CNVD
Non-small cell lung cancer	16651412	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:88015200-88025000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr13:88025000-88026200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr13:88026200-88038800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr13:88038400-88039200	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr13:88056200-88056800	Enhancers	Liver	Liver
6	chr13:88059400-88060000	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
7	chr13:88060000-88062000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr13:88078400-88079600	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr13:88078800-88080000	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr13:88079000-88079400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr13:88079000-88079400	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr13:88079000-88079800	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr13:88079000-88081000	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr13:88079200-88080000	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr13:88110800-88111400	Enhancers	HUVEC	blood vessel
16	chr13:88111400-88111800	Flanking Active TSS	HUVEC	blood vessel
17	chr13:88111800-88113200	Enhancers	HUVEC	blood vessel
18	chr13:88114000-88114400	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr13:88162400-88162800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr13:88166800-88167400	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr13:88167000-88167200	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr13:88167000-88167400	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr13:88169000-88169400	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr13:88178600-88179800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr13:88178600-88180200	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr13:88179000-88179200	Enhancers	NHEK	skin
27	chr13:88179000-88179800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr13:88179000-88180200	Enhancers	HMEC	breast
29	chr13:88179200-88179600	Flanking Active TSS	NHEK	skin
30	chr13:88179200-88180200	Enhancers	Fetal Brain Male	brain
31	chr13:88179600-88180200	Enhancers	NHEK	skin
32	chr13:88188000-88188800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr13:88188000-88188800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr13:88188000-88189400	Enhancers	HMEC	breast
35	chr13:88188200-88188800	Enhancers	NHEK	skin
36	chr13:88189600-88189800	Enhancers	GM12878-XiMat	blood
37	chr13:88192600-88193000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr13:88197800-88198200	Active TSS	Fetal Heart	heart
39	chr13:88205000-88205600	Enhancers	HepG2	liver

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