Variant report

Variant	nsv517362
Chromosome Location	chr19:19846458-19872093
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	ATF3	chr19:19852066-19852400	K562	blood:	n/a	chr19:19852091-19852105
2	BHLHE40	chr19:19849881-19850182	K562	blood:	n/a	n/a
3	BHLHE40	chr19:19861740-19861820	K562	blood:	n/a	chr19:19861759-19861768 chr19:19861759-19861768
4	CEBPB	chr19:19860802-19860934	K562	blood:	n/a	chr19:19860889-19860898 chr19:19860887-19860900 chr19:19860889-19860898 chr19:19860889-19860898 chr19:19860889-19860898
5	CEBPB	chr19:19860725-19860953	HepG2	liver:	n/a	chr19:19860889-19860898 chr19:19860887-19860900 chr19:19860889-19860898 chr19:19860889-19860898 chr19:19860889-19860898
6	CTCF	chr19:19856945-19857039	Hela-S3	cervix:	n/a	n/a
7	CTCF	chr19:19857500-19857650	K562	blood:	n/a	chr19:19857550-19857568 chr19:19857553-19857563 chr19:19857545-19857566 chr19:19857556-19857565 chr19:19857552-19857565
8	CTCF	chr19:19869080-19869230	GM12864	blood:	n/a	n/a
9	CTCF	chr19:19857480-19857630	HEK293	kidney:	n/a	chr19:19857550-19857568 chr19:19857553-19857563 chr19:19857545-19857566 chr19:19857556-19857565 chr19:19857552-19857565
10	CTCF	chr19:19869020-19869384	MCF-7	breast:	n/a	n/a
11	CTCF	chr19:19857320-19857470	GM12871	blood:	n/a	chr19:19857444-19857465 chr19:19857442-19857460
12	CTCF	chr19:19857420-19857570	WERI-Rb-1	eye:	n/a	chr19:19857550-19857568 chr19:19857553-19857563 chr19:19857545-19857566 chr19:19857444-19857465 chr19:19857442-19857460 chr19:19857556-19857565 chr19:19857552-19857565
13	CTCF	chr19:19857500-19857650	NB4	blood:	n/a	chr19:19857550-19857568 chr19:19857553-19857563 chr19:19857545-19857566 chr19:19857556-19857565 chr19:19857552-19857565
14	CTCF	chr19:19869058-19869226	K562	blood:	n/a	n/a
15	CTCF	chr19:19857365-19857702	K562	blood:	n/a	chr19:19857550-19857568 chr19:19857553-19857563 chr19:19857545-19857566 chr19:19857444-19857465 chr19:19857442-19857460 chr19:19857556-19857565 chr19:19857552-19857565
16	CTCF	chr19:19869106-19869247	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr19:19869160-19869310	MCF-7	breast:	n/a	n/a
18	CTCF	chr19:19869040-19869190	HepG2	liver:	n/a	n/a
19	CTCF	chr19:19857301-19857649	H1-hESC	embryonic stem cell:	n/a	chr19:19857550-19857568 chr19:19857553-19857563 chr19:19857545-19857566 chr19:19857444-19857465 chr19:19857442-19857460 chr19:19857556-19857565 chr19:19857552-19857565
20	CTCF	chr19:19869040-19869190	GM12867	blood:	n/a	n/a
21	CTCF	chr19:19850000-19850150	GM12866	blood:	n/a	n/a
22	CTCF	chr19:19857531-19857636	Medullo	brain:	n/a	chr19:19857550-19857568 chr19:19857553-19857563 chr19:19857545-19857566 chr19:19857556-19857565 chr19:19857552-19857565
23	CTCF	chr19:19856977-19856997	Fibrobl	skin:	n/a	n/a
24	CTCF	chr19:19869100-19869250	HCT-116	colon:	n/a	n/a
25	CTCF	chr19:19869060-19869210	GM12873	blood:	n/a	n/a
26	CTCF	chr19:19861961-19862044	K562	blood:	n/a	chr19:19861995-19862013
27	CTCF	chr19:19857386-19857678	K562	blood:	n/a	chr19:19857550-19857568 chr19:19857553-19857563 chr19:19857545-19857566 chr19:19857444-19857465 chr19:19857442-19857460 chr19:19857556-19857565 chr19:19857552-19857565
28	CTCF	chr19:19869060-19869226	HepG2	liver:	n/a	n/a
29	CTCF	chr19:19856940-19857090	GM12873	blood:	n/a	n/a
30	CTCF	chr19:19869220-19869370	GM12872	blood:	n/a	n/a
31	CTCF	chr19:19856939-19857063	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr19:19869160-19869310	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr19:19856900-19857050	NHEK	skin:	n/a	n/a
34	CTCF	chr19:19869200-19869350	GM12871	blood:	n/a	n/a
35	CTCF	chr19:19857480-19857630	WERI-Rb-1	eye:	n/a	chr19:19857550-19857568 chr19:19857553-19857563 chr19:19857545-19857566 chr19:19857556-19857565 chr19:19857552-19857565
36	CTCF	chr19:19869135-19869224	MCF-7	breast:	n/a	n/a
37	CTCF	chr19:19869100-19869250	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr19:19856860-19857010	HepG2	liver:	n/a	n/a
39	CTCF	chr19:19857351-19857652	K562	blood:	n/a	chr19:19857550-19857568 chr19:19857553-19857563 chr19:19857545-19857566 chr19:19857444-19857465 chr19:19857442-19857460 chr19:19857556-19857565 chr19:19857552-19857565
40	CTCF	chr19:19857460-19857610	HCT-116	colon:	n/a	chr19:19857550-19857568 chr19:19857553-19857563 chr19:19857545-19857566 chr19:19857556-19857565 chr19:19857552-19857565
41	CTCF	chr19:19857401-19857704	H1-hESC	embryonic stem cell:	n/a	chr19:19857550-19857568 chr19:19857553-19857563 chr19:19857545-19857566 chr19:19857444-19857465 chr19:19857442-19857460 chr19:19857556-19857565 chr19:19857552-19857565
42	CTCF	chr19:19869080-19869230	HEK293	kidney:	n/a	n/a
43	CTCF	chr19:19857420-19857570	Hela-S3	cervix:	n/a	chr19:19857550-19857568 chr19:19857553-19857563 chr19:19857545-19857566 chr19:19857444-19857465 chr19:19857442-19857460 chr19:19857556-19857565 chr19:19857552-19857565
44	CTCF	chr19:19868973-19869292	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr19:19869051-19869393	K562	blood:	n/a	n/a
46	CTCF	chr19:19857450-19857625	HepG2	liver:	n/a	chr19:19857550-19857568 chr19:19857553-19857563 chr19:19857545-19857566 chr19:19857556-19857565 chr19:19857552-19857565
47	CTCF	chr19:19869100-19869250	HepG2	liver:	n/a	n/a
48	CTCF	chr19:19857480-19857630	GM12872	blood:	n/a	chr19:19857550-19857568 chr19:19857553-19857563 chr19:19857545-19857566 chr19:19857556-19857565 chr19:19857552-19857565
49	CTCF	chr19:19856939-19857035	Spleen_OC	spleen:	n/a	n/a
50	CTCF	chr19:19869080-19869230	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:19855831-19855881	ProgFib	skin:	n/a
2	chr19:19856230-19856280	PFSK-1	brain:	n/a
3	chr19:19856230-19856280	SK-N-MC	brain:	n/a
4	chr19:19856230-19856280	HEK293	kidney:	embryo
5	chr19:19855831-19855881	CMK	blood:	n/a
6	chr19:19856230-19856280	HL-60	blood:	n/a
7	chr19:19855831-19855881	Jurkat	blood:	n/a
8	chr19:19856230-19856280	RPTEC	kidney:	n/a
9	chr19:19856230-19856280	AG04449	skin:	fetal
10	chr19:19856230-19856280	IMR90	lung:	fetal
11	chr19:19856230-19856280	U87	brain:	n/a
12	chr19:19855831-19855881	NHDF-neo	bronchial:	n/a
13	chr19:19855831-19855881	MCF-7	breast:	n/a
14	chr19:19856230-19856280	NHBE	bronchial:	n/a
15	chr19:19855831-19855881	RPTEC	kidney:	n/a
16	chr19:19855831-19855881	HCM	heart:	n/a
17	chr19:19856230-19856280	SK-N-SH	brain:	n/a
18	chr19:19855831-19855881	HAEpiC	amniotic membrane:	n/a
19	chr19:19856230-19856280	K562	blood:	n/a
20	chr19:19855831-19855881	AoSMC	blood vessel:	n/a
21	chr19:19855831-19855881	AG04449	skin:	fetal
22	chr19:19856230-19856280	NT2-D1	testis:	n/a
23	chr19:19855831-19855881	T-47D	breast:	n/a
24	chr19:19856230-19856280	ovcar-3	ovarian:	n/a
25	chr19:19856230-19856280	H1-hESC	embryonic stem cell:	embryo
26	chr19:19855831-19855881	SKMC	muscle:	n/a
27	chr19:19855831-19855881	PFSK-1	brain:	n/a
28	chr19:19855831-19855881	PANC-1	pancreas:	n/a
29	chr19:19856230-19856280	ProgFib	skin:	n/a
30	chr19:19855831-19855881	GM06990	blood:	n/a
31	chr19:19856230-19856280	Jurkat	blood:	n/a
32	chr19:19856230-19856280	GM12878	blood:	n/a
33	chr19:19856230-19856280	HCPEpiC	choroid plexus:	n/a
34	chr19:19856230-19856280	AG10803	skin:	n/a
35	chr19:19856230-19856280	AG09309	skin:	n/a
36	chr19:19855831-19855881	ECC-1	luminal epithelium:	n/a
37	chr19:19855831-19855881	HRE	kidney:	n/a
38	chr19:19855831-19855881	HepG2	liver:	n/a
39	chr19:19855831-19855881	IMR90	lung:	fetal
40	chr19:19856230-19856280	NH-A	brain:	n/a
41	chr19:19855831-19855881	SK-N-MC	brain:	n/a
42	chr19:19855831-19855881	NH-A	brain:	n/a
43	chr19:19855831-19855881	AG10803	skin:	n/a
44	chr19:19856230-19856280	AoSMC	blood vessel:	n/a
45	chr19:19856230-19856280	HAEpiC	amniotic membrane:	n/a
46	chr19:19856230-19856280	HCM	heart:	n/a
47	chr19:19856230-19856280	HRCEpiC	kidney:	n/a
48	chr19:19856230-19856280	HCT-116	colon:	n/a
49	chr19:19855831-19855881	BE2_C	brain:	n/a
50	chr19:19856230-19856280	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:19843487..19845582-chr19:19856344..19858979,2	MCF-7	breast:
2	chr19:19842192..19843794-chr19:19857515..19860071,2	K562	blood:
3	chr19:19842402..19846588-chr19:19867933..19871933,3	MCF-7	breast:
4	chr19:19843963..19845573-chr19:19852096..19854779,2	MCF-7	breast:
5	chr19:19858129..19859838-chr19:19860115..19862862,2	K562	blood:
6	chr19:19857908..19860504-chr19:19872011..19873705,2	K562	blood:
7	chr19:19841771..19844188-chr19:19847201..19851046,3	MCF-7	breast:
8	chr19:19853777..19855300-chr19:19860531..19862733,2	K562	blood:
9	chr19:19772378..19774383-chr19:19858493..19860458,2	K562	blood:
10	chr19:19857908..19860504-chr19:19872011..19873705,2	K562	blood:
11	chr19:19844232..19845828-chr19:19861726..19863362,2	MCF-7	breast:
12	chr19:19861019..19863618-chr19:19865280..19868048,2	K562	blood:
13	chr19:19869687..19871477-chr19:19882175..19885147,2	MCF-7	breast:
14	chr19:19773494..19775880-chr19:19854600..19857474,2	MCF-7	breast:
15	chr19:19857732..19859328-chr19:19976906..19978604,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF14-2	chr19:19855285-19856046	NONHSAT063177
2	lnc-ZNF506-1	chr19:19871967-19872230	ENSG00000266904.1
3	lnc-ZNF506-1	chr19:19868952-19869355	ENSG00000266904.1
4	lnc-ZNF506-1	chr19:19872066-19872230	ENSG00000228642
5	lnc-ZNF506-1	chr19:19872066-19872230	ENSG00000266904.1
6	lnc-ZNF506-1	chr19:19872013-19872230	ENSG00000266904.1
7	lnc-ZNF506-1	chr19:19872018-19872230	NONHSAT063584
8	lnc-ZNF506-1	chr19:19867916-19869355	ENSG00000228642
9	lnc-ZNF506-1	chr19:19868610-19869355	NONHSAT063584
10	lnc-ZNF506-1	chr19:19867185-19867496	ENSG00000228642
11	lnc-ZNF506-1	chr19:19868592-19869355	ENSG00000266904.1
12	lnc-ZNF506-1	chr19:19868175-19869355	ENSG00000228642
13	lnc-ZNF506-1	chr19:19869205-19869355	ENSG00000266904.1

Variant related genes	Relation type
ZNF14	TF binding region
ENSG00000271499	TF binding region
ZNF14	CpG island
ENSG00000271499	CpG island
ENSG00000105726	chromatin interactions
ENSG00000271499	chromatin interactions
ENSG00000105708	chromatin interactions
PDRG1	miRNA target sites
MYCN	miRNA target sites
CGN	miRNA target sites

Extended variants
information (count: 1152 )
Associated
traits (count: 49 )

Variant overlapped rSNPs/rCNVs (count:1152 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs247772	chr19:19846458-19846459	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs551038786	chr19:19846461-19846462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs571117420	chr19:19846557-19846558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs56193587	chr19:19846595-19846596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs115130585	chr19:19846609-19846610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533420312	chr19:19846626-19846627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs547178551	chr19:19846627-19846628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs567040067	chr19:19846636-19846637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs535557889	chr19:19846641-19846642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561843473	chr19:19846669-19846670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs12976586	chr19:19846671-19846672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs568897776	chr19:19846689-19846690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537843775	chr19:19846744-19846745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs149285686	chr19:19846745-19846746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs550516582	chr19:19846759-19846760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577877649	chr19:19846785-19846786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs540108874	chr19:19846794-19846795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553566736	chr19:19846801-19846802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs573486066	chr19:19846811-19846812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs189252395	chr19:19846842-19846843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561841980	chr19:19846843-19846844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566892928	chr19:19846878-19846879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534308000	chr19:19846886-19846887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs530848370	chr19:19846917-19846918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs77657514	chr19:19846924-19846925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs552534472	chr19:19846978-19846979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs533697150	chr19:19847037-19847038	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs114757056	chr19:19847099-19847100	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567107203	chr19:19847106-19847107	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs529491336	chr19:19847115-19847116	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs146246235	chr19:19847144-19847145	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568925481	chr19:19847150-19847151	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs139348247	chr19:19847151-19847152	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs144040836	chr19:19847160-19847161	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571128302	chr19:19847187-19847188	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs146464250	chr19:19847315-19847316	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs553628448	chr19:19847326-19847327	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs573545430	chr19:19847336-19847337	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs192287277	chr19:19847375-19847376	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs555529305	chr19:19847376-19847377	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs575694884	chr19:19847413-19847414	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs539891801	chr19:19847451-19847452	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs537614147	chr19:19847453-19847454	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs557273983	chr19:19847484-19847485	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs577461953	chr19:19847486-19847487	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs182998494	chr19:19847518-19847519	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs560766213	chr19:19847522-19847523	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs187092628	chr19:19847549-19847550	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs398130	chr19:19847559-19847560	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs191844002	chr19:19847579-19847580	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:49)

Disease	PMID	Source
Prostate cancer	16573809	CNVD
Lung cancer	17297452	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Medulloblastoma	16783165	CNVD
Monoclonal gammopathy of undetermined significance	17077331	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
Basal cell lymphoma	21115979	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21364760	CNVD
Acute monocytic leukemia	16498392	CNVD
Lung cancer	18438408	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Cancer	17440070	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Nasopharyngeal cancer	20548289	CNVD

Chromatin state (count:76 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:19844400-19847000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr19:19844400-19848200	Weak transcription	K562	blood
3	chr19:19844400-19848600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr19:19847000-19847200	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr19:19848200-19848600	Enhancers	K562	blood
6	chr19:19848200-19851200	Weak transcription	Stomach Smooth Muscle	stomach
7	chr19:19848600-19849000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr19:19849000-19849800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr19:19849600-19850400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr19:19849800-19850400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr19:19850000-19850200	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
12	chr19:19850400-19857000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr19:19852800-19853800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr19:19853000-19862600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr19:19853200-19855600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr19:19853400-19853600	Bivalent/Poised TSS	HepG2	liver
17	chr19:19853600-19853800	Bivalent Enhancer	HepG2	liver
18	chr19:19853800-19854000	Flanking Bivalent TSS/Enh	HepG2	liver
19	chr19:19854000-19854800	Bivalent Enhancer	HepG2	liver
20	chr19:19854600-19854800	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
21	chr19:19856600-19859000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr19:19856600-19862200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr19:19857000-19858000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr19:19857200-19857400	Bivalent/Poised TSS	Fetal Brain Female	brain
25	chr19:19857400-19857600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr19:19858000-19858400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr19:19858400-19863200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr19:19859000-19859200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr19:19859000-19859600	ZNF genes & repeats	Spleen	Spleen
30	chr19:19859200-19865000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr19:19859600-19860800	Weak transcription	Spleen	Spleen
32	chr19:19859800-19870800	Weak transcription	Placenta Amnion	Placenta Amnion
33	chr19:19860400-19861400	Weak transcription	Gastric	stomach
34	chr19:19860800-19862400	ZNF genes & repeats	Spleen	Spleen
35	chr19:19861000-19875000	Weak transcription	Brain Angular Gyrus	brain
36	chr19:19861400-19862200	Strong transcription	Gastric	stomach
37	chr19:19862200-19862800	Enhancers	Pancreas	Pancrea
38	chr19:19862200-19869200	Weak transcription	Gastric	stomach
39	chr19:19862400-19862800	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
40	chr19:19862400-19869000	Weak transcription	Spleen	Spleen
41	chr19:19862800-19874000	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr19:19862800-19886400	Weak transcription	Pancreas	Pancrea
43	chr19:19865200-19865600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr19:19865200-19886400	Weak transcription	Right Ventricle	heart
45	chr19:19865400-19873800	Weak transcription	Ovary	ovary
46	chr19:19865600-19879000	Weak transcription	Brain Substantia Nigra	brain
47	chr19:19865800-19866200	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
48	chr19:19866200-19868600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr19:19866200-19886000	Weak transcription	Brain Hippocampus Middle	brain
50	chr19:19866600-19868400	Weak transcription	Brain Cingulate Gyrus	brain

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