Variant report

Variant	nsv579079
Chromosome Location	chr19:24267575-24308487
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:469)
CpG islands
(count:366)
Chromatin interactive
region (count:23)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:469 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:24269634-24269992	K562	blood:	n/a	n/a
2	ARID3A	chr19:24277965-24278090	HepG2	liver:	n/a	n/a
3	ATF1	chr19:24269666-24270047	K562	blood:	n/a	n/a
4	ATF2	chr19:24269632-24269953	GM12878	blood:	n/a	n/a
5	BACH1	chr19:24270502-24270514	K562	blood:	n/a	n/a
6	BCL3	chr19:24269688-24270514	A549	lung:	n/a	n/a
7	BCL3	chr19:24269800-24270463	A549	lung:	n/a	n/a
8	BCL3	chr19:24269789-24270455	GM12878	blood:	n/a	n/a
9	BCLAF1	chr19:24269773-24270344	GM12878	blood:	n/a	n/a
10	BHLHE40	chr19:24269821-24270044	K562	blood:	n/a	n/a
11	CBX3	chr19:24269975-24270349	K562	blood:	n/a	n/a
12	CEBPB	chr19:24269699-24270116	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr19:24269736-24270125	K562	blood:	n/a	n/a
14	CEBPB	chr19:24268405-24268573	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr19:24269746-24270087	K562	blood:	n/a	n/a
16	CEBPB	chr19:24274254-24274360	K562	blood:	n/a	n/a
17	CEBPB	chr19:24270144-24270151	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr19:24268418-24268618	K562	blood:	n/a	n/a
19	CEBPB	chr19:24269821-24270021	A549	lung:	n/a	n/a
20	CEBPD	chr19:24269710-24270404	K562	blood:	n/a	n/a
21	CEBPD	chr19:24269764-24270215	K562	blood:	n/a	n/a
22	CHD1	chr19:24269530-24270611	IMR90	lung:	n/a	n/a
23	CHD1	chr19:24270004-24270498	GM12878	blood:	n/a	n/a
24	CHD2	chr19:24269745-24270337	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr19:24269727-24270371	GM12878	blood:	n/a	n/a
26	CHD2	chr19:24269818-24270242	K562	blood:	n/a	n/a
27	CHD2	chr19:24269829-24270027	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr19:24269797-24270053	A549	lung:	n/a	n/a
29	CREB1	chr19:24269696-24270445	A549	lung:	n/a	n/a
30	CTCF	chr19:24269980-24270130	SK-N-SH_RA	brain:	n/a	chr19:24270081-24270089
31	CTCF	chr19:24270280-24270430	A549	lung:	n/a	n/a
32	CTCF	chr19:24270260-24270410	AG09319	gingival:	n/a	n/a
33	CTCF	chr19:24270280-24270430	AoAF	blood vessel:	n/a	n/a
34	CTCF	chr19:24270062-24270085	MCF-7	breast:	n/a	n/a
35	CTCF	chr19:24270260-24270410	AG04450	lung:	n/a	n/a
36	CTCF	chr19:24270340-24270490	HAc	cerebellar:	n/a	n/a
37	CTCF	chr19:24270000-24270150	BE2_C	brain:	n/a	chr19:24270081-24270089
38	CTCF	chr19:24270240-24270390	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr19:24270260-24270410	NHLF	lung:	n/a	n/a
40	CTCF	chr19:24270240-24270390	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr19:24270220-24270370	AG09309	skin:	n/a	n/a
42	CTCF	chr19:24270220-24270370	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr19:24270280-24270430	HVMF	connective:	n/a	n/a
44	CTCF	chr19:24270420-24270570	HFF	foreskin:	n/a	n/a
45	CTCF	chr19:24270326-24270350	MCF-7	breast:	n/a	n/a
46	CTCF	chr19:24270300-24270450	HA-sp	spinal cord:	n/a	n/a
47	CTCF	chr19:24270328-24270356	Lung_OC	lung:	n/a	n/a
48	CTCF	chr19:24270060-24270157	Lung_OC	lung:	n/a	chr19:24270081-24270089
49	CTCF	chr19:24270240-24270390	HCFaa	heart:	n/a	n/a
50	CTCF	chr19:24270220-24270370	GM12864	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:24269890-24269940	NT2-D1	testis:	n/a
2	chr19:24270468-24270518	GM12891	blood:	n/a
3	chr19:24270007-24270057	U87	brain:	n/a
4	chr19:24269890-24269940	HRCEpiC	kidney:	n/a
5	chr19:24269968-24270018	Hela-S3	cervix:	n/a
6	chr19:24269890-24269940	RPTEC	kidney:	n/a
7	chr19:24269890-24269940	MCF-7	breast:	n/a
8	chr19:24270073-24270123	SK-N-SH_RA	brain:	n/a
9	chr19:24270007-24270057	GM06990	blood:	n/a
10	chr19:24269975-24270025	HepG2	liver:	n/a
11	chr19:24269890-24269940	HepG2	liver:	n/a
12	chr19:24269890-24269940	Hela-S3	cervix:	n/a
13	chr19:24269890-24269940	HCT-116	colon:	n/a
14	chr19:24270007-24270057	AG09319	gingival:	n/a
15	chr19:24270073-24270123	CMK	blood:	n/a
16	chr19:24269890-24269940	HCF	heart:	n/a
17	chr19:24270007-24270057	SK-N-SH	brain:	n/a
18	chr19:24270007-24270057	NHDF-neo	bronchial:	n/a
19	chr19:24270073-24270123	AG09319	gingival:	n/a
20	chr19:24270073-24270123	HAEpiC	amniotic membrane:	n/a
21	chr19:24270468-24270518	HCF	heart:	n/a
22	chr19:24269890-24269940	HMEC	breast:	n/a
23	chr19:24270073-24270123	HCT-116	colon:	n/a
24	chr19:24269975-24270025	HCPEpiC	choroid plexus:	n/a
25	chr19:24270073-24270123	HEEpiC	esophagus:	n/a
26	chr19:24270007-24270057	RPTEC	kidney:	n/a
27	chr19:24269975-24270025	AG04449	skin:	fetal
28	chr19:24270468-24270518	PANC-1	pancreas:	n/a
29	chr19:24270007-24270057	NHBE	bronchial:	n/a
30	chr19:24269975-24270025	Hela-S3	cervix:	n/a
31	chr19:24270468-24270518	NB4	blood:	n/a
32	chr19:24270073-24270123	HPAEpiC	pulmonary alveolar:	n/a
33	chr19:24269975-24270025	SK-N-MC	brain:	n/a
34	chr19:24270073-24270123	HNPCEpiC	eye:	n/a
35	chr19:24270468-24270518	HEK293	kidney:	embryo
36	chr19:24269975-24270025	HMEC	breast:	n/a
37	chr19:24270073-24270123	SAEC	small airway:	n/a
38	chr19:24269968-24270018	Jurkat	blood:	n/a
39	chr19:24269975-24270025	A549	lung:	n/a
40	chr19:24270073-24270123	U87	brain:	n/a
41	chr19:24269968-24270018	AoSMC	blood vessel:	n/a
42	chr19:24269968-24270018	HRE	kidney:	n/a
43	chr19:24269975-24270025	RPTEC	kidney:	n/a
44	chr19:24270073-24270123	HRCEpiC	kidney:	n/a
45	chr19:24270073-24270123	HCM	heart:	n/a
46	chr19:24269975-24270025	GM12892	blood:	n/a
47	chr19:24270007-24270057	HRE	kidney:	n/a
48	chr19:24270468-24270518	ProgFib	skin:	n/a
49	chr19:24270468-24270518	SK-N-SH	brain:	n/a
50	chr19:24270007-24270057	LNCaP	prostate:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:24216051..24217841-chr19:24269020..24271219,2	MCF-7	breast:
2	chr19:24269869..24271737-chr19:24281128..24282836,2	MCF-7	breast:
3	chr19:24266915..24268889-chr19:24271542..24273329,2	MCF-7	breast:
4	chr19:24097706..24100500-chr19:24267529..24270344,3	K562	blood:
5	chr19:24269806..24272597-chr19:24274053..24277432,4	K562	blood:
6	chr19:24269191..24271795-chr19:24273714..24276847,3	MCF-7	breast:
7	chr19:24269735..24271787-chr19:24289462..24293668,3	MCF-7	breast:
8	chr19:24278737..24281409-chr19:24289986..24291875,2	K562	blood:
9	chr19:24278737..24281409-chr19:24289986..24291875,2	K562	blood:
10	chr19:23299713..23300295-chr19:24269911..24270643,3	Hela-S3	cervix:
11	chr19:24269869..24271737-chr19:24281128..24282836,2	MCF-7	breast:
12	chr19:24269801..24271346-chr19:24277835..24280239,2	K562	blood:
13	chr19:24264646..24268309-chr19:24268403..24270705,3	MCF-7	breast:
14	chr19:24273653..24275947-chr19:24283763..24286065,2	K562	blood:
15	chr19:24216492..24217018-chr19:24270056..24270717,2	Hela-S3	cervix:
16	chr19:24214637..24216513-chr19:24268176..24271021,2	K562	blood:
17	chr19:24266915..24268889-chr19:24271542..24273329,2	MCF-7	breast:
18	chr19:24269855..24272221-chr19:24274367..24277034,2	K562	blood:
19	chr19:24269481..24270366-chr8:29940201..29940789,2	NB4	blood:
20	chr19:24214690..24216513-chr19:24269521..24272423,2	K562	blood:
21	chr19:24273653..24275947-chr19:24283763..24286065,2	K562	blood:
22	chr19:24269905..24270406-chr19:47616316..47616816,2	Hela-S3	cervix:
23	chr19:24269211..24271747-chr19:24290443..24293090,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF726-3	chr19:24286988-24290154	NONHSAT063958
2	lnc-ZNF681-5	chr19:24281227-24281782	NONHSAT063956

No data

Variant related genes	Relation type
ZNF254	TF binding region
ENSG00000268058	TF binding region
ZNF254	CpG island
ENSG00000268058	CpG island
ENSG00000142230	chromatin interactions
ENSG00000268362	chromatin interactions
ENSG00000213967	chromatin interactions
ENSG00000213096	chromatin interactions
ENSG00000133872	chromatin interactions
ENSG00000183850	chromatin interactions
ENSG00000268058	chromatin interactions
ENSG00000272256	chromatin interactions

Extended variants
information (count: 1596 )
Associated
traits (count: 43 )

Variant overlapped rSNPs/rCNVs (count:1596 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4932942	chr19:24267575-24267576	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs189250346	chr19:24267600-24267601	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs559721076	chr19:24267601-24267602	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs143384310	chr19:24267678-24267679	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs371572997	chr19:24267683-24267684	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs192466010	chr19:24267686-24267687	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs376021410	chr19:24267694-24267695	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs150066308	chr19:24267735-24267736	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs202206627	chr19:24267740-24267741	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs79334864	chr19:24267751-24267752	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs566577210	chr19:24267795-24267796	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs551649008	chr19:24267880-24267881	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs529278502	chr19:24267890-24267891	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs530640713	chr19:24267947-24267948	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs4932943	chr19:24267955-24267956	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs567331918	chr19:24267970-24267971	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs140232144	chr19:24267976-24267977	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs183099520	chr19:24268028-24268029	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs571651295	chr19:24268029-24268030	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs189593292	chr19:24268038-24268039	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs66670702	chr19:24268109-24268110	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs557140233	chr19:24268126-24268127	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs575396759	chr19:24268210-24268211	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs369827913	chr19:24268211-24268212	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs547673608	chr19:24268228-24268229	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs186678473	chr19:24268229-24268230	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs375891924	chr19:24268245-24268246	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs536775051	chr19:24268253-24268254	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs199560972	chr19:24268266-24268267	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs137914157	chr19:24268361-24268362	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs142459406	chr19:24268400-24268401	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs540311117	chr19:24268498-24268499	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs565276839	chr19:24268510-24268511	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs558423038	chr19:24268559-24268560	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs527406048	chr19:24268577-24268578	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs73524123	chr19:24268582-24268583	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs545284079	chr19:24268587-24268588	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs563494134	chr19:24268633-24268634	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs530645654	chr19:24268651-24268652	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs549145625	chr19:24268694-24268695	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs138598183	chr19:24268742-24268743	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs113727469	chr19:24268766-24268767	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs567569646	chr19:24268779-24268780	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs570867756	chr19:24268780-24268781	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs144590524	chr19:24268848-24268849	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs191179122	chr19:24268901-24268902	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs536445536	chr19:24268964-24268965	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs550038689	chr19:24268965-24268966	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs369886667	chr19:24268975-24268976	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs555138101	chr19:24268979-24268980	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 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	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
Renal cell carcinoma	18194544	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Autism	19287141	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1721 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:24236200-24269400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr19:24239800-24269600	Weak transcription	Small Intestine	intestine
3	chr19:24242000-24269800	Weak transcription	Stomach Mucosa	stomach
4	chr19:24242400-24269400	Weak transcription	Fetal Thymus	thymus
5	chr19:24243600-24269600	Weak transcription	NHLF	lung
6	chr19:24244200-24269400	Weak transcription	HUVEC	blood vessel
7	chr19:24245200-24270000	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr19:24250200-24269200	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr19:24251000-24269400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr19:24251200-24269200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr19:24251200-24269600	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr19:24251200-24269800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr19:24251400-24269600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr19:24251600-24269600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr19:24251600-24269600	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr19:24251800-24269000	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr19:24251800-24269400	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr19:24255800-24269600	Weak transcription	Osteobl	bone
19	chr19:24256200-24269600	Weak transcription	Rectal Smooth Muscle	rectum
20	chr19:24256200-24269600	Weak transcription	HSMM	muscle
21	chr19:24256600-24269600	Weak transcription	NHDF-Ad	bronchial
22	chr19:24256600-24269800	Weak transcription	Colon Smooth Muscle	Colon
23	chr19:24256800-24269600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr19:24256800-24270000	Weak transcription	Fetal Brain Male	brain
25	chr19:24257000-24269400	Weak transcription	Brain Hippocampus Middle	brain
26	chr19:24257000-24269400	Weak transcription	Pancreas	Pancrea
27	chr19:24257000-24269600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr19:24257000-24269800	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr19:24257000-24270000	Weak transcription	Aorta	Aorta
30	chr19:24257200-24269200	Weak transcription	Primary B cells from peripheral blood	blood
31	chr19:24257200-24269400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr19:24257200-24269800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr19:24257400-24269400	Weak transcription	Thymus	Thymus
34	chr19:24257400-24269600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr19:24257400-24269800	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr19:24257400-24269800	Weak transcription	Ovary	ovary
37	chr19:24257400-24270000	Weak transcription	Gastric	stomach
38	chr19:24257600-24269400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr19:24257600-24269400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr19:24257600-24269400	Weak transcription	Adipose Nuclei	Adipose
41	chr19:24257600-24269400	Weak transcription	Duodenum Mucosa	Duodenum
42	chr19:24257600-24269400	Weak transcription	Lung	lung
43	chr19:24257600-24269400	Weak transcription	Rectal Mucosa Donor 29	rectum
44	chr19:24257600-24269400	Weak transcription	Hela-S3	cervix
45	chr19:24257600-24269600	Weak transcription	HMEC	breast
46	chr19:24257800-24269200	Weak transcription	Primary B cells from cord blood	blood
47	chr19:24257800-24269600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr19:24257800-24269800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr19:24258000-24269600	Weak transcription	Fetal Intestine Large	intestine
50	chr19:24258000-24269800	Weak transcription	Brain Anterior Caudate	brain

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