Variant report

Variant	nsv562778
Chromosome Location	chr13:95992979-96027507
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:147)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:147 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr13:96001635-96001886	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr13:96012862-96013164	K562	blood:	n/a	n/a
3	CBX3	chr13:96015553-96015829	K562	blood:	n/a	n/a
4	CBX3	chr13:96008953-96009226	K562	blood:	n/a	n/a
5	CEBPB	chr13:96001631-96001874	K562	blood:	n/a	n/a
6	CEBPB	chr13:96022472-96022715	IMR90	lung:	n/a	chr13:96022629-96022640
7	CEBPB	chr13:96022569-96022728	HepG2	liver:	n/a	chr13:96022629-96022640
8	CEBPB	chr13:96004765-96005063	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr13:96022480-96022768	K562	blood:	n/a	chr13:96022629-96022640
10	CTCF	chr13:96004731-96004837	Gliobla	brain:	n/a	n/a
11	CTCF	chr13:95994700-95994850	GM12873	blood:	n/a	n/a
12	CTCF	chr13:96004749-96004822	MCF-7	breast:	n/a	n/a
13	CTCF	chr13:96021789-96021840	Kidney_OC	kidney:	n/a	n/a
14	CTCF	chr13:96004540-96004690	HFF-Myc	foreskin:	n/a	n/a
15	CTCF	chr13:96006337-96006441	Spleen_OC	spleen:	n/a	n/a
16	CTCF	chr13:96004740-96004890	RPTEC	kidney:	n/a	n/a
17	CTCF	chr13:96004720-96004870	HRPEpiC	eye:	n/a	n/a
18	CTCF	chr13:96006620-96006770	RPTEC	kidney:	n/a	n/a
19	CTCF	chr13:96004720-96004870	RPTEC	kidney:	n/a	n/a
20	CTCF	chr13:96004700-96004850	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr13:96004700-96004850	HRE	kidney:	n/a	n/a
22	CTCF	chr13:96004664-96004889	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr13:96004719-96004845	MCF-7	breast:	n/a	n/a
24	CTCF	chr13:96006600-96006750	AG04450	lung:	n/a	n/a
25	CTCF	chr13:96006559-96006675	K562	blood:	n/a	n/a
26	CTCF	chr13:96015920-96016070	GM12864	blood:	n/a	n/a
27	CTCF	chr13:96004692-96004867	NHEK	skin:	n/a	n/a
28	CTCF	chr13:96004700-96004850	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr13:96006440-96006797	K562	blood:	n/a	n/a
30	CTCF	chr13:95999859-95999866	Kidney_OC	kidney:	n/a	n/a
31	CTCF	chr13:96006540-96006690	HMEC	breast:	n/a	n/a
32	CTCF	chr13:96004700-96004850	NHEK	skin:	n/a	n/a
33	CTCF	chr13:96004693-96004848	MCF-7	breast:	n/a	n/a
34	CTCF	chr13:96004700-96004850	HEEpiC	esophagus:	n/a	n/a
35	CTCF	chr13:96012942-96013126	K562	blood:	n/a	n/a
36	CTCF	chr13:96004680-96004830	SAEC	small airway:	n/a	n/a
37	CTCF	chr13:96004676-96004874	MCF-7	breast:	n/a	n/a
38	CTCF	chr13:96006611-96006697	Lung_OC	lung:	n/a	n/a
39	CTCF	chr13:96004762-96004802	HepG2	liver:	n/a	n/a
40	CTCF	chr13:96006484-96006517	LNCaP	prostate:	n/a	n/a
41	CTCF	chr13:96025846-96025897	GM13977	blood:	n/a	n/a
42	CTCF	chr13:96004640-96004790	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr13:96004690-96004865	MCF-7	breast:	n/a	n/a
44	E2F4	chr13:96004890-96005181	MCF10A-Er-Src	breast:	n/a	n/a
45	EP300	chr13:96019845-96020073	SK-N-SH_RA	brain:	n/a	n/a
46	EP300	chr13:96001655-96001818	K562	blood:	n/a	chr13:96001754-96001763
47	EP300	chr13:96019712-96020054	SK-N-SH_RA	brain:	n/a	n/a
48	EP300	chr13:96009877-96009886	K562	blood:	n/a	n/a
49	EP300	chr13:96012950-96013110	K562	blood:	n/a	n/a
50	FOS	chr13:96021341-96021524	MCF10A-Er-Src	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:96008021-96008071	HCT-116	colon:	n/a
2	chr13:96008021-96008071	NT2-D1	testis:	n/a
3	chr13:96008021-96008071	HCPEpiC	choroid plexus:	n/a
4	chr13:96008021-96008071	NB4	blood:	n/a
5	chr13:96008021-96008071	ECC-1	luminal epithelium:	n/a
6	chr13:96008021-96008071	AG04449	skin:	fetal
7	chr13:96008021-96008071	IMR90	lung:	fetal
8	chr13:96008021-96008071	NHBE	bronchial:	n/a
9	chr13:96008021-96008071	AG04450	lung:	fetal
10	chr13:96008021-96008071	HCM	heart:	n/a
11	chr13:96008021-96008071	PrEC	prostate:	n/a
12	chr13:96008021-96008071	AG10803	skin:	n/a
13	chr13:96008021-96008071	U87	brain:	n/a
14	chr13:96008021-96008071	HMEC	breast:	n/a
15	chr13:96008021-96008071	NH-A	brain:	n/a
16	chr13:96008021-96008071	AG09309	skin:	n/a
17	chr13:96008021-96008071	HUVEC	blood vessel:	n/a
18	chr13:96008021-96008071	CMK	blood:	n/a
19	chr13:96008021-96008071	PFSK-1	brain:	n/a
20	chr13:96008021-96008071	ovcar-3	ovarian:	n/a
21	chr13:96008021-96008071	T-47D	breast:	n/a
22	chr13:96008021-96008071	HRE	kidney:	n/a
23	chr13:96008021-96008071	Jurkat	blood:	n/a
24	chr13:96008021-96008071	HPAEpiC	pulmonary alveolar:	n/a
25	chr13:96008021-96008071	HNPCEpiC	eye:	n/a
26	chr13:96008021-96008071	SKMC	muscle:	n/a
27	chr13:96008021-96008071	Caco-2	colon:	n/a
28	chr13:96008021-96008071	GM12891	blood:	n/a
29	chr13:96008021-96008071	HCF	heart:	n/a
30	chr13:96008021-96008071	H1-hESC	embryonic stem cell:	embryo
31	chr13:96008021-96008071	A549	lung:	n/a
32	chr13:96008021-96008071	SK-N-SH	brain:	n/a
33	chr13:96008021-96008071	ProgFib	skin:	n/a
34	chr13:96008021-96008071	HEK293	kidney:	embryo
35	chr13:96008021-96008071	HL-60	blood:	n/a
36	chr13:96008021-96008071	AoSMC	blood vessel:	n/a
37	chr13:96008021-96008071	HEEpiC	esophagus:	n/a
38	chr13:96008021-96008071	HIPEpiC	eye:	n/a
39	chr13:96008021-96008071	HRCEpiC	kidney:	n/a
40	chr13:96008021-96008071	AG09319	gingival:	n/a
41	chr13:96008021-96008071	BJ	skin:	n/a
42	chr13:96008021-96008071	MCF-7	breast:	n/a
43	chr13:96008021-96008071	HAEpiC	amniotic membrane:	n/a
44	chr13:96008021-96008071	BE2_C	brain:	n/a
45	chr13:96008021-96008071	K562	blood:	n/a
46	chr13:96008021-96008071	SK-N-SH_RA	brain:	n/a
47	chr13:96008021-96008071	RPTEC	kidney:	n/a
48	chr13:96008021-96008071	NHDF-neo	bronchial:	n/a
49	chr13:96008021-96008071	Hepatocyte	liver:	n/a
50	chr13:96008021-96008071	LNCaP	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr13:95990065..95992069-chr13:95994982..95997042,2	K562	blood:
2	chr13:96010392..96012474-chr13:96022109..96025076,2	K562	blood:
3	chr13:96010392..96012474-chr13:96022109..96025076,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABCC4-2	chr13:96003796-96003967	NONHSAT034758

No data

Variant related genes	Relation type
RNY4P27	TF binding region
RNY4P27	CpG island

Extended variants
information (count: 1223 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1223 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11617735	chr13:95992979-95992980	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs527991055	chr13:95992983-95992984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs138582409	chr13:95992996-95992997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs34194995	chr13:95993005-95993006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184745804	chr13:95993035-95993036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs550520670	chr13:95993051-95993052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs189202251	chr13:95993065-95993066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs11617741	chr13:95993079-95993080	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs535583163	chr13:95993087-95993088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs549319561	chr13:95993088-95993089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs113395570	chr13:95993153-95993154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs535063906	chr13:95993176-95993177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs180962665	chr13:95993200-95993201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs578257872	chr13:95993202-95993203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs533065088	chr13:95993211-95993212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs537618238	chr13:95993291-95993292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs557292713	chr13:95993292-95993293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs573633325	chr13:95993293-95993294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs146321081	chr13:95993295-95993296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs559070104	chr13:95993327-95993328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs572484316	chr13:95993329-95993330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs376719994	chr13:95993339-95993340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs10508011	chr13:95993350-95993351	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs372801739	chr13:95993396-95993397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs564806617	chr13:95993415-95993416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs530738825	chr13:95993424-95993425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs550706571	chr13:95993458-95993459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538012238	chr13:95993483-95993484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs569568809	chr13:95993498-95993499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs560936131	chr13:95993516-95993517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs375952845	chr13:95993524-95993525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs386380303	chr13:95993525-95993526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs202027123	chr13:95993527-95993528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs11618008	chr13:95993528-95993529	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs113266941	chr13:95993544-95993545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs568329466	chr13:95993555-95993556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs529938535	chr13:95993576-95993577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs374839740	chr13:95993599-95993600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs2211050	chr13:95993605-95993606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs191333873	chr13:95993621-95993622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs534998134	chr13:95993638-95993639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs7322526	chr13:95993655-95993656	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs77310018	chr13:95993668-95993669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs75611145	chr13:95993782-95993783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs142452699	chr13:95993829-95993830	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574150710	chr13:95993862-95993863	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs2250912	chr13:95993924-95993925	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs115930364	chr13:95993944-95993945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs35313353	chr13:95993952-95993953	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs151312807	chr13:95993955-95993956	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
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
Metanephric adenoma	20802469	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
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Rhabdomyosarcoma	17210683	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	19651601	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Intellectual disability	22102821	CNVD
Burkitt''s lymphoma	20823134	CNVD

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:95986600-95993800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr13:95990400-95996200	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr13:95991200-95993000	Enhancers	Rectal Smooth Muscle	rectum
4	chr13:95991600-95993000	Enhancers	Colon Smooth Muscle	Colon
5	chr13:95993000-95994200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr13:95993800-95994200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr13:95993800-95994200	Enhancers	Osteobl	bone
8	chr13:95996000-95996800	Enhancers	HUVEC	blood vessel
9	chr13:95996200-95996400	Enhancers	Skeletal Muscle Male	skeletal muscle
10	chr13:95999800-96000200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr13:95999800-96000200	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr13:96001200-96001800	Enhancers	Psoas Muscle	Psoas
13	chr13:96001400-96001800	Enhancers	K562	blood
14	chr13:96001600-96002000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr13:96001800-96005800	Weak transcription	K562	blood
16	chr13:96003800-96004200	Enhancers	HepG2	liver
17	chr13:96004200-96004600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr13:96004200-96006800	Weak transcription	HepG2	liver
19	chr13:96004400-96005200	Enhancers	Hela-S3	cervix
20	chr13:96004600-96005200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr13:96005000-96005400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr13:96005200-96008000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr13:96005400-96007000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr13:96005800-96006200	Enhancers	HMEC	breast
25	chr13:96005800-96007000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr13:96005800-96007000	Enhancers	K562	blood
27	chr13:96006000-96008000	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr13:96006000-96008200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr13:96006000-96008400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr13:96006200-96007200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr13:96006400-96009600	Enhancers	Liver	Liver
32	chr13:96006600-96007000	Enhancers	Brain Hippocampus Middle	brain
33	chr13:96006600-96007400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr13:96006600-96008000	Enhancers	Brain Anterior Caudate	brain
35	chr13:96006600-96008200	Enhancers	Stomach Mucosa	stomach
36	chr13:96006800-96007200	Enhancers	Brain Angular Gyrus	brain
37	chr13:96006800-96007400	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr13:96006800-96007600	Enhancers	HepG2	liver
39	chr13:96006800-96008000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr13:96006800-96008000	Enhancers	Brain Substantia Nigra	brain
41	chr13:96006800-96008200	Enhancers	HUVEC	blood vessel
42	chr13:96006800-96008400	Enhancers	Fetal Stomach	stomach
43	chr13:96007000-96007400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr13:96007000-96007400	Enhancers	Brain Germinal Matrix	brain
45	chr13:96007000-96007400	Flanking Active TSS	Brain Hippocampus Middle	brain
46	chr13:96007000-96007400	Enhancers	Colon Smooth Muscle	Colon
47	chr13:96007000-96007400	Enhancers	Gastric	stomach
48	chr13:96007000-96008200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr13:96007000-96008200	Enhancers	Fetal Kidney	kidney
50	chr13:96007000-96008200	Enhancers	Fetal Lung	lung

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