Variant report

Variant	nsv579464
Chromosome Location	chr19:37858660-37881556
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:572)
CpG islands
(count:796)
Chromatin interactive
region (count:6)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:572 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:37861654-37862744	HepG2	liver:	n/a	n/a
2	ATF1	chr19:37861774-37862351	K562	blood:	n/a	n/a
3	ATF2	chr19:37861461-37862444	GM12878	blood:	n/a	n/a
4	ATF2	chr19:37861866-37862149	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr19:37861740-37862270	GM12878	blood:	n/a	n/a
6	ATF2	chr19:37861886-37862212	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr19:37861668-37862146	GM12878	blood:	n/a	n/a
8	ATF3	chr19:37861795-37861990	K562	blood:	n/a	n/a
9	ATF3	chr19:37861394-37862600	A549	lung:	n/a	n/a
10	BACH1	chr19:37861660-37862501	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL3	chr19:37861361-37862743	A549	lung:	n/a	n/a
12	BCL3	chr19:37861682-37862682	GM12878	blood:	n/a	n/a
13	BCLAF1	chr19:37861465-37862373	GM12878	blood:	n/a	n/a
14	BCLAF1	chr19:37861539-37862504	GM12878	blood:	n/a	n/a
15	BHLHE40	chr19:37861601-37862021	K562	blood:	n/a	n/a
16	BHLHE40	chr19:37861458-37862467	GM12878	blood:	n/a	chr19:37862143-37862159
17	BHLHE40	chr19:37861635-37862492	HepG2	liver:	n/a	chr19:37862143-37862159
18	BRCA1	chr19:37861740-37862192	HepG2	liver:	n/a	n/a
19	BRCA1	chr19:37861775-37862384	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr19:37861772-37862220	GM12878	blood:	n/a	n/a
21	BRCA1	chr19:37861728-37862459	Hela-S3	cervix:	n/a	n/a
22	CCNT2	chr19:37861708-37862295	K562	blood:	n/a	n/a
23	CEBPB	chr19:37876513-37876823	HepG2	liver:	n/a	n/a
24	CEBPB	chr19:37876558-37876844	A549	lung:	n/a	n/a
25	CEBPB	chr19:37861849-37862122	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr19:37876534-37876835	IMR90	lung:	n/a	n/a
27	CEBPB	chr19:37861577-37862510	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr19:37868038-37868365	A549	lung:	n/a	n/a
29	CEBPB	chr19:37861623-37862421	HepG2	liver:	n/a	n/a
30	CEBPD	chr19:37861596-37861828	HepG2	liver:	n/a	n/a
31	CEBPD	chr19:37861906-37862425	HepG2	liver:	n/a	n/a
32	CHD1	chr19:37876875-37876950	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD1	chr19:37862055-37862511	GM12878	blood:	n/a	n/a
34	CHD2	chr19:37861649-37862378	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr19:37861795-37862229	K562	blood:	n/a	n/a
36	CHD2	chr19:37861508-37862519	GM12878	blood:	n/a	n/a
37	CHD2	chr19:37861729-37862223	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr19:37861620-37862316	HepG2	liver:	n/a	n/a
39	CREB1	chr19:37861659-37862334	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chr19:37861535-37862527	A549	lung:	n/a	n/a
41	CREB1	chr19:37861728-37862268	ECC-1	luminal epithelium:	n/a	n/a
42	CREB1	chr19:37861685-37862243	A549	lung:	n/a	n/a
43	CREB1	chr19:37861475-37862342	GM12878	blood:	n/a	n/a
44	CREB1	chr19:37861706-37862232	K562	blood:	n/a	n/a
45	CREB1	chr19:37861433-37862532	GM12878	blood:	n/a	n/a
46	CREB1	chr19:37861555-37862386	HepG2	liver:	n/a	n/a
47	CREB1	chr19:37861738-37862189	K562	blood:	n/a	n/a
48	CREB1	chr19:37861610-37862390	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr19:37861477-37862692	HepG2	liver:	n/a	n/a
50	CTBP2	chr19:37861611-37862322	H1-hESC	embryonic stem cell:	n/a	n/a

(count:796 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:37862220-37862270	BE2_C	brain:	n/a
2	chr19:37862272-37862322	SK-N-SH_RA	brain:	n/a
3	chr19:37861925-37861975	RPTEC	kidney:	n/a
4	chr19:37862220-37862270	BE2_C	brain:	n/a
5	chr19:37862272-37862322	SK-N-SH_RA	brain:	n/a
6	chr19:37861925-37861975	RPTEC	kidney:	n/a
7	chr19:37862220-37862270	Caco-2	colon:	n/a
8	chr19:37858855-37858905	ovcar-3	ovarian:	n/a
9	chr19:37862232-37862282	AG04450	lung:	fetal
10	chr19:37858855-37858905	NHDF-neo	bronchial:	n/a
11	chr19:37862232-37862282	GM19239	blood:	n/a
12	chr19:37858855-37858905	LNCaP	prostate:	n/a
13	chr19:37861546-37861596	GM12878	blood:	n/a
14	chr19:37861925-37861975	HCPEpiC	choroid plexus:	n/a
15	chr19:37861935-37861985	SK-N-MC	brain:	n/a
16	chr19:37862220-37862270	U87	brain:	n/a
17	chr19:37865648-37865698	AG04450	lung:	fetal
18	chr19:37861984-37862034	AG04449	skin:	fetal
19	chr19:37861935-37861985	PFSK-1	brain:	n/a
20	chr19:37861546-37861596	Hepatocyte	liver:	n/a
21	chr19:37861707-37861757	HEEpiC	esophagus:	n/a
22	chr19:37858855-37858905	Hela-S3	cervix:	n/a
23	chr19:37861652-37861702	BJ	skin:	n/a
24	chr19:37861925-37861975	NHBE	bronchial:	n/a
25	chr19:37862272-37862322	IMR90	lung:	fetal
26	chr19:37861986-37862036	SK-N-SH_RA	brain:	n/a
27	chr19:37861984-37862034	NH-A	brain:	n/a
28	chr19:37865648-37865698	CMK	blood:	n/a
29	chr19:37865648-37865698	HUVEC	blood vessel:	n/a
30	chr19:37862045-37862095	GM12892	blood:	n/a
31	chr19:37862272-37862322	GM06990	blood:	n/a
32	chr19:37865648-37865698	RPTEC	kidney:	n/a
33	chr19:37861546-37861596	AG09309	skin:	n/a
34	chr19:37861935-37861985	HPAEpiC	pulmonary alveolar:	n/a
35	chr19:37861986-37862036	GM12891	blood:	n/a
36	chr19:37861546-37861596	Hela-S3	cervix:	n/a
37	chr19:37861986-37862036	NHBE	bronchial:	n/a
38	chr19:37861986-37862036	ECC-1	luminal epithelium:	n/a
39	chr19:37862045-37862095	HL-60	blood:	n/a
40	chr19:37862220-37862270	ProgFib	skin:	n/a
41	chr19:37861984-37862034	HPAEpiC	pulmonary alveolar:	n/a
42	chr19:37862232-37862282	Caco-2	colon:	n/a
43	chr19:37865648-37865698	ProgFib	skin:	n/a
44	chr19:37862045-37862095	PANC-1	pancreas:	n/a
45	chr19:37861707-37861757	LNCaP	prostate:	n/a
46	chr19:37858855-37858905	ECC-1	luminal epithelium:	n/a
47	chr19:37861652-37861702	SKMC	muscle:	n/a
48	chr19:37861984-37862034	HEK293	kidney:	embryo
49	chr19:37862232-37862282	ProgFib	skin:	n/a
50	chr19:37861546-37861596	NHBE	bronchial:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:37855409..37858293-chr19:37876540..37879521,2	MCF-7	breast:
2	chr19:37860446..37862285-chr19:38041060..38043682,2	K562	blood:
3	chr19:37867252..37869425-chr19:37869859..37871564,2	MCF-7	breast:
4	chr19:37851946..37854387-chr19:37859960..37862069,2	MCF-7	breast:
5	chr19:37861996..37864602-chr19:37959702..37962085,2	MCF-7	breast:
6	chr19:37867252..37869425-chr19:37869859..37871564,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF527-2	chr19:37865060-37865133	NONHSAT066108
2	lnc-ZNF569-3	chr19:37869794-37870014	l_1679_chr19:37869793-37874605_adrenal
3	lnc-ZNF569-3	chr19:37874109-37874614	l_1679_chr19:37869793-37874605_adrenal
4	lnc-ZNF527-2	chr19:37870022-37870148	NONHSAT066108
5	lnc-ZNF527-2	chr19:37861963-37862128	NONHSAT066108
6	lnc-ZNF527-2	chr19:37870389-37870594	NONHSAT066108

No data

Variant related genes	Relation type
ZNF527	TF binding region
ZNF527	CpG island
ENSG00000267470	chromatin interactions
ENSG00000171827	chromatin interactions
ENSG00000171817	chromatin interactions
ENSG00000181666	chromatin interactions
ENSG00000196437	chromatin interactions

Extended variants
information (count: 765 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:765 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs256739	chr19:37858660-37858661	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs563948479	chr19:37858721-37858722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs528056755	chr19:37858762-37858763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs10422320	chr19:37858782-37858783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs540148116	chr19:37858823-37858824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs181787061	chr19:37858839-37858840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529100020	chr19:37858859-37858860	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs550352180	chr19:37858863-37858864	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs185217063	chr19:37858880-37858881	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs533248300	chr19:37858903-37858904	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs551823602	chr19:37859115-37859116	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs375232689	chr19:37859149-37859150	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs373515600	chr19:37859178-37859179	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs73629665	chr19:37859249-37859250	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs190494225	chr19:37859271-37859272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs567954804	chr19:37859304-37859305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs538478997	chr19:37859325-37859326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs556463509	chr19:37859340-37859341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs536662632	chr19:37859363-37859364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs578104104	chr19:37859427-37859428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs556507591	chr19:37859487-37859488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545598227	chr19:37859515-37859516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560088986	chr19:37859534-37859535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557796660	chr19:37859583-37859584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs572511149	chr19:37859584-37859585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs576406287	chr19:37859592-37859593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs561688237	chr19:37859779-37859780	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs528595511	chr19:37859836-37859837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113960859	chr19:37859900-37859901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570183504	chr19:37859901-37859902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs113730735	chr19:37859905-37859906	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
32	rs544031144	chr19:37859924-37859925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562561515	chr19:37859931-37859932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs141743791	chr19:37859951-37859952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs374699017	chr19:37859975-37859976	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs570470368	chr19:37860011-37860012	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs56986819	chr19:37860024-37860025	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs76876292	chr19:37860042-37860043	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs527731394	chr19:37860114-37860115	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs549385984	chr19:37860252-37860253	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs571996519	chr19:37860288-37860289	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs375070981	chr19:37860334-37860335	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs567991850	chr19:37860349-37860350	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs256738	chr19:37860368-37860369	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs150555213	chr19:37860491-37860492	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs538515462	chr19:37860595-37860596	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs550417024	chr19:37860602-37860603	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs139625873	chr19:37860609-37860610	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs539178254	chr19:37860612-37860613	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs557617137	chr19:37860641-37860642	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	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
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Glioma	17123091	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Wilms tumour	21544195	CNVD
Mental retardation	19951919	CNVD
19q13.11 deletion syndrome	22378287	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Lung cancer	21569311	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1186 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:37826600-37861600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr19:37854200-37861200	Weak transcription	Psoas Muscle	Psoas
3	chr19:37854200-37861400	Weak transcription	Small Intestine	intestine
4	chr19:37855000-37861400	Weak transcription	Fetal Heart	heart
5	chr19:37855000-37861600	Weak transcription	Aorta	Aorta
6	chr19:37855200-37860800	Weak transcription	Brain Cingulate Gyrus	brain
7	chr19:37855200-37861000	Weak transcription	Right Ventricle	heart
8	chr19:37855200-37861200	Weak transcription	Left Ventricle	heart
9	chr19:37855200-37861400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr19:37855200-37861400	Weak transcription	Fetal Brain Male	brain
11	chr19:37855200-37861400	Weak transcription	NH-A	brain
12	chr19:37855400-37860400	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr19:37855400-37860800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr19:37855400-37860800	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr19:37855400-37861000	Weak transcription	Fetal Kidney	kidney
16	chr19:37855400-37861400	Weak transcription	Hela-S3	cervix
17	chr19:37855600-37860600	Weak transcription	Stomach Smooth Muscle	stomach
18	chr19:37855600-37860800	Weak transcription	Brain Angular Gyrus	brain
19	chr19:37855600-37861200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr19:37855600-37861200	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr19:37855600-37861400	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr19:37855600-37861400	Weak transcription	Ovary	ovary
23	chr19:37855600-37861400	Weak transcription	HSMMtube	muscle
24	chr19:37855600-37861400	Weak transcription	Osteobl	bone
25	chr19:37855800-37860800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr19:37855800-37861200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr19:37855800-37861400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr19:37855800-37861400	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr19:37856400-37861400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr19:37856400-37861400	Weak transcription	Brain Hippocampus Middle	brain
31	chr19:37856600-37860800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr19:37856600-37860800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr19:37856800-37861200	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr19:37856800-37861200	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr19:37856800-37861200	Weak transcription	Fetal Lung	lung
36	chr19:37857000-37860400	Weak transcription	Dnd41	blood
37	chr19:37857000-37860800	Weak transcription	Adipose Nuclei	Adipose
38	chr19:37857000-37861200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr19:37857000-37861400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr19:37857200-37861200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr19:37857400-37860800	Weak transcription	NHDF-Ad	bronchial
42	chr19:37859000-37859200	ZNF genes & repeats	A549	lung
43	chr19:37859200-37860200	Weak transcription	A549	lung
44	chr19:37860200-37861000	ZNF genes & repeats	A549	lung
45	chr19:37860400-37860600	Enhancers	Dnd41	blood
46	chr19:37860400-37861000	ZNF genes & repeats	Liver	Liver
47	chr19:37860400-37861200	Enhancers	Primary T cells from cord blood	blood
48	chr19:37860400-37861400	Active TSS	Skeletal Muscle Female	skeletal muscle
49	chr19:37860600-37860800	Enhancers	Duodenum Mucosa	Duodenum
50	chr19:37860600-37861200	Active TSS	Primary T helper cells PMA-I stimulated	--

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