Variant report

Variant	esv3349738
Chromosome Location	chr19:24058940-24150711
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:408)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:408 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:24097373-24097798	K562	blood:	n/a	n/a
2	ATF1	chr19:24082792-24082903	K562	blood:	n/a	n/a
3	ATF3	chr19:24097347-24097690	K562	blood:	n/a	n/a
4	CBX3	chr19:24097376-24097802	K562	blood:	n/a	n/a
5	CEBPB	chr19:24137391-24137485	IMR90	lung:	n/a	n/a
6	CEBPB	chr19:24137373-24138010	HepG2	liver:	n/a	chr19:24137849-24137860
7	CEBPB	chr19:24091167-24091261	A549	lung:	n/a	n/a
8	CEBPB	chr19:24090268-24090459	A549	lung:	n/a	n/a
9	CEBPB	chr19:24097420-24097714	K562	blood:	n/a	n/a
10	CEBPB	chr19:24137722-24138015	IMR90	lung:	n/a	chr19:24137849-24137860
11	CEBPB	chr19:24098849-24098997	K562	blood:	n/a	n/a
12	CEBPB	chr19:24097506-24097590	A549	lung:	n/a	n/a
13	CEBPB	chr19:24072689-24072942	A549	lung:	n/a	n/a
14	CEBPB	chr19:24097393-24097705	MCF-7	breast:	n/a	n/a
15	CEBPB	chr19:24097435-24097683	IMR90	lung:	n/a	n/a
16	CEBPB	chr19:24108284-24108419	H1-hESC	embryonic stem cell:	n/a	chr19:24108307-24108318
17	CEBPB	chr19:24097376-24097743	K562	blood:	n/a	n/a
18	CEBPB	chr19:24150478-24150629	HepG2	liver:	n/a	n/a
19	CEBPB	chr19:24089814-24089980	A549	lung:	n/a	n/a
20	CEBPB	chr19:24065481-24065571	HepG2	liver:	n/a	n/a
21	CEBPB	chr19:24108206-24108466	A549	lung:	n/a	chr19:24108307-24108318
22	CEBPB	chr19:24137774-24137977	K562	blood:	n/a	chr19:24137849-24137860
23	CEBPB	chr19:24089351-24089528	A549	lung:	n/a	n/a
24	CEBPB	chr19:24108238-24108422	K562	blood:	n/a	chr19:24108307-24108318
25	CEBPB	chr19:24081510-24082196	A549	lung:	n/a	n/a
26	CEBPB	chr19:24100626-24100978	MCF-7	breast:	n/a	n/a
27	CEBPB	chr19:24108215-24108391	HepG2	liver:	n/a	chr19:24108307-24108318
28	CEBPB	chr19:24104270-24104301	K562	blood:	n/a	n/a
29	CEBPB	chr19:24137704-24138014	A549	lung:	n/a	chr19:24137849-24137860
30	CEBPB	chr19:24072664-24072864	HepG2	liver:	n/a	n/a
31	CEBPB	chr19:24067770-24067949	HepG2	liver:	n/a	n/a
32	CEBPB	chr19:24108200-24108395	IMR90	lung:	n/a	chr19:24108307-24108318
33	CEBPB	chr19:24081588-24082206	HepG2	liver:	n/a	n/a
34	CEBPZ	chr19:24065321-24065511	HepG2	liver:	n/a	n/a
35	CEBPZ	chr19:24070604-24070807	HepG2	liver:	n/a	n/a
36	CHD2	chr19:24097507-24098117	K562	blood:	n/a	n/a
37	CHD2	chr19:24097496-24097766	GM12878	blood:	n/a	n/a
38	CREB1	chr19:24097434-24097763	A549	lung:	n/a	n/a
39	CTCF	chr19:24140820-24140970	HMF	breast:	n/a	n/a
40	CTCF	chr19:24140640-24140790	AG10803	skin:	n/a	n/a
41	CTCF	chr19:24087497-24087527	GM10266	blood:	n/a	n/a
42	CTCF	chr19:24097820-24098070	AG04449	skin:	n/a	n/a
43	CTCF	chr19:24101899-24101916	GM20000	blood:	n/a	n/a
44	CTCF	chr19:24069956-24070010	GM13976	blood:	n/a	n/a
45	CTCF	chr19:24097880-24098030	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr19:24097820-24097970	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr19:24106500-24106537	GM10248	blood:	n/a	n/a
48	CTCF	chr19:24140934-24141042	GM20000	blood:	n/a	n/a
49	CTCF	chr19:24140660-24140810	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr19:24110520-24110543	Kidney_OC	kidney:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:24097753-24097803	HRPEpiC	eye:	n/a
2	chr19:24097753-24097803	HRE	kidney:	n/a
3	chr19:24097753-24097803	HL-60	blood:	n/a
4	chr19:24097753-24097803	HIPEpiC	eye:	n/a
5	chr19:24097753-24097803	HAEpiC	amniotic membrane:	n/a
6	chr19:24097753-24097803	PFSK-1	brain:	n/a
7	chr19:24097753-24097803	GM12878	blood:	n/a
8	chr19:24097753-24097803	AG09319	gingival:	n/a
9	chr19:24097753-24097803	GM12891	blood:	n/a
10	chr19:24097753-24097803	SK-N-SH	brain:	n/a
11	chr19:24097753-24097803	PANC-1	pancreas:	n/a
12	chr19:24097753-24097803	K562	blood:	n/a
13	chr19:24097753-24097803	Hepatocyte	liver:	n/a
14	chr19:24097753-24097803	AG09309	skin:	n/a
15	chr19:24097753-24097803	BE2_C	brain:	n/a
16	chr19:24097753-24097803	PrEC	prostate:	n/a
17	chr19:24097753-24097803	U87	brain:	n/a
18	chr19:24097753-24097803	AG04449	skin:	fetal
19	chr19:24097753-24097803	NHDF-neo	bronchial:	n/a
20	chr19:24097753-24097803	SK-N-SH_RA	brain:	n/a
21	chr19:24097753-24097803	HNPCEpiC	eye:	n/a
22	chr19:24097753-24097803	MCF-7	breast:	n/a
23	chr19:24097753-24097803	GM12892	blood:	n/a
24	chr19:24097753-24097803	ECC-1	luminal epithelium:	n/a
25	chr19:24097753-24097803	HCPEpiC	choroid plexus:	n/a
26	chr19:24097753-24097803	NT2-D1	testis:	n/a
27	chr19:24097753-24097803	GM19239	blood:	n/a
28	chr19:24097753-24097803	SKMC	muscle:	n/a
29	chr19:24097753-24097803	NB4	blood:	n/a
30	chr19:24097753-24097803	HEEpiC	esophagus:	n/a
31	chr19:24097753-24097803	SAEC	small airway:	n/a
32	chr19:24097753-24097803	HRCEpiC	kidney:	n/a
33	chr19:24097753-24097803	HUVEC	blood vessel:	n/a
34	chr19:24097753-24097803	IMR90	lung:	fetal
35	chr19:24097753-24097803	NH-A	brain:	n/a
36	chr19:24097753-24097803	LNCaP	prostate:	n/a
37	chr19:24097753-24097803	HPAEpiC	pulmonary alveolar:	n/a
38	chr19:24097753-24097803	T-47D	breast:	n/a
39	chr19:24097753-24097803	HCF	heart:	n/a
40	chr19:24097753-24097803	Jurkat	blood:	n/a
41	chr19:24097753-24097803	GM06990	blood:	n/a
42	chr19:24097753-24097803	ovcar-3	ovarian:	n/a
43	chr19:24097753-24097803	AG10803	skin:	n/a
44	chr19:24097753-24097803	HCM	heart:	n/a
45	chr19:24097753-24097803	BJ	skin:	n/a
46	chr19:24097753-24097803	HEK293	kidney:	embryo
47	chr19:24097753-24097803	CMK	blood:	n/a
48	chr19:24097753-24097803	AG04450	lung:	fetal
49	chr19:24097753-24097803	SK-N-MC	brain:	n/a
50	chr19:24097753-24097803	Hela-S3	cervix:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:24097706..24100500-chr19:24267529..24270344,3	K562	blood:
2	chr19:24093000..24094884-chr19:24096609..24099585,2	K562	blood:
3	chr19:24121908..24123986-chr19:24125230..24127009,2	MCF-7	breast:
4	chr19:24095542..24098509-chr19:24107269..24108889,2	K562	blood:
5	chr19:24090411..24092500-chr19:24096453..24099025,2	K562	blood:
6	chr19:24121908..24123986-chr19:24125230..24127009,2	MCF-7	breast:
7	chr19:24098019..24099596-chr19:24100994..24103194,2	K562	blood:
8	chr19:24113206..24114972-chr19:24116698..24118505,2	K562	blood:
9	chr19:24097916..24099582-chr19:24104881..24106475,2	K562	blood:
10	chr19:24098019..24099596-chr19:24100994..24103194,2	K562	blood:
11	chr19:24097916..24099582-chr19:24104881..24106475,2	K562	blood:
12	chr19:24127186..24129970-chr19:24140101..24141968,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF681-2	chr19:24140533-24141028	NONHSAT063949
2	lnc-ZNF681-2	chr19:24101883-24103000	ENSG00000104777
3	lnc-RPSAP58-4	chr19:24110590-24112089	ENSG00000269397.1
4	lnc-ZNF681-2	chr19:24140533-24140732	ENSG00000104777
5	lnc-ZNF681-2	chr19:24134972-24135238	ENSG00000104777
6	lnc-ZNF681-2	chr19:24134950-24135238	NONHSAT063949
7	lnc-ZNF254-2	chr19:24118022-24118975	NONHSAT063946

No data

Variant related genes	Relation type
ZNF726	TF binding region
ENSG00000269397	TF binding region
ENSG00000267924	TF binding region
ZNF92P3	TF binding region
ENSG00000269289	TF binding region
ZNF726	CpG island
ENSG00000269397	CpG island
ENSG00000267924	CpG island
ZNF92P3	CpG island
ENSG00000269289	CpG island
ENSG00000213967	chromatin interactions
ENSG00000213096	chromatin interactions
ENSG00000269289	chromatin interactions
ENSG00000269421	chromatin interactions
RALB	miRNA target sites
PGRMC1	miRNA target sites

Extended variants
information (count: 3279 )
Associated
traits (count: 43 )

Variant overlapped rSNPs/rCNVs (count:3279 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561935264	chr19:24058963-24058964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs141927388	chr19:24058979-24058980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs8105540	chr19:24059015-24059016	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs8105541	chr19:24059016-24059017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs532999506	chr19:24059026-24059027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs551408048	chr19:24059048-24059049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs373144008	chr19:24059056-24059057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs570316791	chr19:24059080-24059081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs145752939	chr19:24059097-24059098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs535139645	chr19:24059108-24059109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs373193597	chr19:24059112-24059113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555322085	chr19:24059122-24059123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs190227276	chr19:24059126-24059127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs8105380	chr19:24059150-24059151	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs182517925	chr19:24059166-24059167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs73525817	chr19:24059250-24059251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs556956232	chr19:24059256-24059257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs187514611	chr19:24059257-24059258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs543346098	chr19:24059275-24059276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs17725202	chr19:24059276-24059277	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs138683821	chr19:24059277-24059278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs376378306	chr19:24059293-24059294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs142749794	chr19:24059301-24059302	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs559359458	chr19:24059305-24059306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs150334263	chr19:24059361-24059362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs34150406	chr19:24059424-24059425	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs563290599	chr19:24059433-24059434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs111410718	chr19:24059451-24059452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs66482561	chr19:24059452-24059453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs58927924	chr19:24059454-24059455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs191623537	chr19:24059475-24059476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs112041263	chr19:24059487-24059488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs549681309	chr19:24059498-24059499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs74825083	chr19:24059507-24059508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
35	rs73021235	chr19:24059508-24059509	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs138012564	chr19:24059519-24059520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs549715004	chr19:24059528-24059529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs374718394	chr19:24059561-24059562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs571378100	chr19:24059594-24059595	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs149510242	chr19:24059597-24059598	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs556921227	chr19:24059629-24059630	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs568937290	chr19:24059634-24059635	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs562108901	chr19:24059652-24059653	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs555673254	chr19:24059660-24059661	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs573862359	chr19:24059666-24059667	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs530888295	chr19:24059681-24059682	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs541174309	chr19:24059696-24059697	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs552915189	chr19:24059700-24059701	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs577779789	chr19:24059715-24059716	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs116189225	chr19:24059719-24059720	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:43)

Disease	PMID	Source
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Colorectal cancer	20459617	CNVD
Ductal carcinoma	22052326	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Renal cell carcinoma	18194544	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:702 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:24048200-24059600	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr19:24054600-24060000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr19:24058200-24060000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr19:24059200-24060200	Enhancers	Fetal Lung	lung
5	chr19:24059200-24060400	Enhancers	Gastric	stomach
6	chr19:24059200-24060600	Enhancers	Placenta	Placenta
7	chr19:24059200-24060600	Enhancers	Rectal Mucosa Donor 29	rectum
8	chr19:24059600-24060400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr19:24059600-24060600	Enhancers	Placenta Amnion	Placenta Amnion
10	chr19:24059800-24060200	Enhancers	Colonic Mucosa	Colon
11	chr19:24060000-24060200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
12	chr19:24060000-24060600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr19:24060000-24060800	ZNF genes & repeats	Lung	lung
14	chr19:24060400-24065200	Weak transcription	Gastric	stomach
15	chr19:24060800-24065200	Weak transcription	Lung	lung
16	chr19:24061400-24063400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
17	chr19:24063000-24063400	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
18	chr19:24064600-24067600	Enhancers	Liver	Liver
19	chr19:24064800-24066000	Enhancers	Rectal Mucosa Donor 31	rectum
20	chr19:24065000-24065400	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
21	chr19:24065000-24065400	Enhancers	Colonic Mucosa	Colon
22	chr19:24065000-24065600	Active TSS	Rectal Mucosa Donor 29	rectum
23	chr19:24065200-24065600	Enhancers	Gastric	stomach
24	chr19:24065200-24065600	Enhancers	Lung	lung
25	chr19:24065400-24065800	Enhancers	Stomach Mucosa	stomach
26	chr19:24065600-24065800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
27	chr19:24065600-24070600	Weak transcription	Gastric	stomach
28	chr19:24065800-24066400	Active TSS	Rectal Mucosa Donor 29	rectum
29	chr19:24066400-24069000	Weak transcription	Rectal Mucosa Donor 29	rectum
30	chr19:24067600-24068000	Flanking Active TSS	Liver	Liver
31	chr19:24068000-24071600	Enhancers	Liver	Liver
32	chr19:24069000-24070000	Enhancers	Colonic Mucosa	Colon
33	chr19:24069000-24070400	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
34	chr19:24069600-24071600	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
35	chr19:24070000-24070800	Weak transcription	Colonic Mucosa	Colon
36	chr19:24070400-24071000	Active TSS	Rectal Mucosa Donor 29	rectum
37	chr19:24070600-24071400	Enhancers	Gastric	stomach
38	chr19:24070800-24071200	Active TSS	Colonic Mucosa	Colon
39	chr19:24071000-24071400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
40	chr19:24071400-24071600	ZNF genes & repeats	Colonic Mucosa	Colon
41	chr19:24071400-24071600	Active TSS	Rectal Mucosa Donor 29	rectum
42	chr19:24079200-24080000	Enhancers	Liver	Liver
43	chr19:24079400-24080200	Enhancers	Colonic Mucosa	Colon
44	chr19:24079400-24080400	ZNF genes & repeats	Adipose Nuclei	Adipose
45	chr19:24080200-24084000	Weak transcription	Colonic Mucosa	Colon
46	chr19:24083400-24084000	Enhancers	Rectal Mucosa Donor 29	rectum
47	chr19:24084000-24085000	Enhancers	Colonic Mucosa	Colon
48	chr19:24087800-24088200	ZNF genes & repeats	Liver	Liver
49	chr19:24088200-24089200	Weak transcription	Liver	Liver
50	chr19:24089200-24093000	Enhancers	Liver	Liver

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