Variant report

Variant	nsv963134
Chromosome Location	chr19:41429958-41437852
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:34)
CpG islands
(count:122)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:34 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:41434897-41435097	K562	blood:	n/a	n/a
2	BACH1	chr19:41430483-41430507	K562	blood:	n/a	n/a
3	CCNT2	chr19:41434884-41435092	K562	blood:	n/a	n/a
4	CEBPB	chr19:41434742-41435118	K562	blood:	n/a	n/a
5	CEBPB	chr19:41430599-41430915	HepG2	liver:	n/a	n/a
6	CEBPB	chr19:41434755-41435152	K562	blood:	n/a	n/a
7	CEBPB	chr19:41430580-41430916	A549	lung:	n/a	n/a
8	CEBPB	chr19:41430620-41430805	K562	blood:	n/a	n/a
9	CEBPB	chr19:41434826-41435086	K562	blood:	n/a	n/a
10	CTCF	chr19:41430640-41430790	A549	lung:	n/a	n/a
11	CTCF	chr19:41436101-41436138	MCF-7	breast:	n/a	n/a
12	CTCF	chr19:41437073-41439938	A549	lung:	n/a	n/a
13	CUX1	chr19:41435256-41435570	K562	blood:	n/a	n/a
14	CUX1	chr19:41434360-41434765	K562	blood:	n/a	n/a
15	EP300	chr19:41434756-41435138	K562	blood:	n/a	n/a
16	ESR1	chr19:41434874-41435116	T-47D	breast:	n/a	n/a
17	ESR1	chr19:41434788-41435139	T-47D	breast:	n/a	n/a
18	ESR1	chr19:41434822-41435116	T-47D	breast:	n/a	n/a
19	ESR1	chr19:41434821-41435131	T-47D	breast:	n/a	n/a
20	ESR1	chr19:41434736-41435100	T-47D	breast:	n/a	n/a
21	ESR1	chr19:41434838-41435089	T-47D	breast:	n/a	n/a
22	FOS	chr19:41430453-41430653	MCF10A-Er-Src	breast:	n/a	n/a
23	FOSL2	chr19:41430005-41430846	A549	lung:	n/a	n/a
24	GATA1	chr19:41434163-41435362	K562	blood:	n/a	n/a
25	GATA2	chr19:41434798-41435151	K562	blood:	n/a	n/a
26	GATA3	chr19:41434778-41435095	T-47D	breast:	n/a	n/a
27	IRF1	chr19:41434848-41434955	K562	blood:	n/a	n/a
28	JUND	chr19:41434830-41435079	K562	blood:	n/a	n/a
29	MYC	chr19:41434838-41435089	K562	blood:	n/a	n/a
30	MYC	chr19:41435981-41436123	MCF-7	breast:	n/a	n/a
31	RCOR1	chr19:41434896-41435075	K562	blood:	n/a	n/a
32	TAL1	chr19:41434800-41435135	K562	blood:	n/a	n/a
33	TEAD4	chr19:41434733-41435174	K562	blood:	n/a	n/a
34	TEAD4	chr19:41434744-41435190	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:41430077-41430127	HIPEpiC	eye:	n/a
2	chr19:41430189-41430239	SAEC	small airway:	n/a
3	chr19:41430189-41430239	ECC-1	luminal epithelium:	n/a
4	chr19:41430189-41430239	HRCEpiC	kidney:	n/a
5	chr19:41430189-41430239	AG09319	gingival:	n/a
6	chr19:41430189-41430239	AoSMC	blood vessel:	n/a
7	chr19:41430189-41430239	PFSK-1	brain:	n/a
8	chr19:41430189-41430239	HAEpiC	amniotic membrane:	n/a
9	chr19:41430189-41430239	SKMC	muscle:	n/a
10	chr19:41430189-41430239	NT2-D1	testis:	n/a
11	chr19:41430189-41430239	GM06990	blood:	n/a
12	chr19:41430189-41430239	RPTEC	kidney:	n/a
13	chr19:41430189-41430239	HIPEpiC	eye:	n/a
14	chr19:41430077-41430127	SK-N-SH	brain:	n/a
15	chr19:41430189-41430239	HEK293	kidney:	embryo
16	chr19:41430077-41430127	GM12892	blood:	n/a
17	chr19:41430189-41430239	H1-hESC	embryonic stem cell:	embryo
18	chr19:41430189-41430239	BJ	skin:	n/a
19	chr19:41430077-41430127	GM12878	blood:	n/a
20	chr19:41430189-41430239	HRE	kidney:	n/a
21	chr19:41430189-41430239	NH-A	brain:	n/a
22	chr19:41430077-41430127	HepG2	liver:	n/a
23	chr19:41430077-41430127	K562	blood:	n/a
24	chr19:41430077-41430127	AG09319	gingival:	n/a
25	chr19:41430189-41430239	AG04449	skin:	fetal
26	chr19:41430077-41430127	ECC-1	luminal epithelium:	n/a
27	chr19:41430189-41430239	Jurkat	blood:	n/a
28	chr19:41430189-41430239	MCF10A-Er-Src	breast:	n/a
29	chr19:41430189-41430239	HCT-116	colon:	n/a
30	chr19:41430189-41430239	K562	blood:	n/a
31	chr19:41430189-41430239	A549	lung:	n/a
32	chr19:41430189-41430239	NHDF-neo	bronchial:	n/a
33	chr19:41430189-41430239	PANC-1	pancreas:	n/a
34	chr19:41430077-41430127	Hela-S3	cervix:	n/a
35	chr19:41430189-41430239	HepG2	liver:	n/a
36	chr19:41430077-41430127	HMEC	breast:	n/a
37	chr19:41430077-41430127	NH-A	brain:	n/a
38	chr19:41430077-41430127	HNPCEpiC	eye:	n/a
39	chr19:41430077-41430127	Caco-2	colon:	n/a
40	chr19:41430077-41430127	HCT-116	colon:	n/a
41	chr19:41430077-41430127	HCF	heart:	n/a
42	chr19:41430189-41430239	HMEC	breast:	n/a
43	chr19:41430077-41430127	HRCEpiC	kidney:	n/a
44	chr19:41430189-41430239	HUVEC	blood vessel:	n/a
45	chr19:41430189-41430239	BE2_C	brain:	n/a
46	chr19:41430189-41430239	HCF	heart:	n/a
47	chr19:41430077-41430127	SK-N-MC	brain:	n/a
48	chr19:41430077-41430127	T-47D	breast:	n/a
49	chr19:41430077-41430127	ProgFib	skin:	n/a
50	chr19:41430189-41430239	SK-N-SH	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:41400931..41403268-chr19:41432541..41435329,2	K562	blood:
2	chr19:41429883..41432599-chr19:41435321..41438137,2	MCF-7	breast:
3	chr19:41433604..41436108-chr19:41440713..41443622,2	MCF-7	breast:
4	chr19:41436490..41439337-chr19:41447432..41449781,2	MCF-7	breast:
5	chr19:41303143..41305588-chr19:41428304..41431722,3	MCF-7	breast:
6	chr19:41303781..41306051-chr19:41433024..41435492,2	MCF-7	breast:
7	chr19:41435849..41437489-chr19:41440022..41442246,2	MCF-7	breast:

No data

Variant related genes	Relation type
CYP2B7P	TF binding region
CYP2B7P	CpG island
ENSG00000269858	chromatin interactions
ENSG00000256612	chromatin interactions

Extended variants
information (count: 302 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:302 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534443347	chr19:41429964-41429965	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs192544366	chr19:41429966-41429967	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs145276544	chr19:41429977-41429978	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs139008091	chr19:41429991-41429992	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs529227404	chr19:41429994-41429995	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs142214964	chr19:41429995-41429996	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs34418474	chr19:41430151-41430152	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs543794612	chr19:41430153-41430154	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs559582941	chr19:41430196-41430197	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs146400592	chr19:41430219-41430220	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs376905133	chr19:41430239-41430240	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs532819778	chr19:41430242-41430243	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs115334099	chr19:41430243-41430244	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs541554979	chr19:41430254-41430255	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs559562113	chr19:41430257-41430258	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs202042326	chr19:41430280-41430281	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs541721564	chr19:41430281-41430282	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs112620024	chr19:41430309-41430310	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs530761743	chr19:41430314-41430315	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs552133444	chr19:41430330-41430331	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs570125848	chr19:41430361-41430362	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs113177009	chr19:41430367-41430368	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs528144509	chr19:41430381-41430382	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs4062241	chr19:41430402-41430403	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs4062242	chr19:41430404-41430405	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs551356322	chr19:41430409-41430410	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs546292146	chr19:41430455-41430456	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs565895057	chr19:41430472-41430473	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs184739211	chr19:41430519-41430520	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs548545633	chr19:41430590-41430591	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs112298484	chr19:41430601-41430602	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs386809304	chr19:41430610-41430611	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs116257965	chr19:41430611-41430612	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs116740487	chr19:41430614-41430615	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs571743358	chr19:41430633-41430634	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs536710747	chr19:41430779-41430780	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs373555271	chr19:41430786-41430787	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs549167012	chr19:41430796-41430797	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs535075285	chr19:41430801-41430802	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs553516239	chr19:41430861-41430862	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs574878134	chr19:41430862-41430863	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs187892246	chr19:41430877-41430878	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs192989033	chr19:41430889-41430890	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs575459223	chr19:41430940-41430941	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs185233790	chr19:41430969-41430970	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs545798377	chr19:41430984-41430985	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs563689205	chr19:41430985-41430986	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs528083920	chr19:41431006-41431007	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs546230607	chr19:41431018-41431019	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs561442540	chr19:41431020-41431021	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
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
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
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Genital abnormality	22378287	CNVD
Hypospadia	22378287	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD

Chromatin state (count:74 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41426400-41430200	Enhancers	Fetal Intestine Large	intestine
2	chr19:41426400-41430200	Enhancers	Fetal Intestine Small	intestine
3	chr19:41428000-41430200	Weak transcription	Hela-S3	cervix
4	chr19:41428000-41430800	Enhancers	Rectal Mucosa Donor 31	rectum
5	chr19:41428200-41430200	Weak transcription	Lung	lung
6	chr19:41428400-41430200	Weak transcription	Placenta	Placenta
7	chr19:41429000-41434200	Weak transcription	K562	blood
8	chr19:41429200-41434600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr19:41429600-41430200	Weak transcription	Ovary	ovary
10	chr19:41429600-41430400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr19:41429600-41430400	Flanking Active TSS	Liver	Liver
12	chr19:41429600-41430400	Enhancers	Colonic Mucosa	Colon
13	chr19:41429600-41430600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr19:41429600-41430800	Flanking Active TSS	Duodenum Mucosa	Duodenum
15	chr19:41429600-41430800	Enhancers	Gastric	stomach
16	chr19:41429800-41430000	Enhancers	Pancreas	Pancrea
17	chr19:41429800-41430000	Flanking Active TSS	Stomach Mucosa	stomach
18	chr19:41429800-41430000	Flanking Bivalent TSS/Enh	A549	lung
19	chr19:41429800-41430200	Active TSS	Rectal Mucosa Donor 29	rectum
20	chr19:41430000-41430200	Enhancers	Sigmoid Colon	Sigmoid Colon
21	chr19:41430000-41430200	Enhancers	Stomach Mucosa	stomach
22	chr19:41430000-41430200	Bivalent Enhancer	HepG2	liver
23	chr19:41430000-41430400	Bivalent Enhancer	A549	lung
24	chr19:41430200-41430400	Flanking Active TSS	Fetal Intestine Small	intestine
25	chr19:41430200-41430400	Enhancers	Placenta	Placenta
26	chr19:41430200-41430400	Enhancers	Ovary	ovary
27	chr19:41430200-41430400	Enhancers	Rectal Mucosa Donor 29	rectum
28	chr19:41430200-41430400	Flanking Active TSS	Stomach Mucosa	stomach
29	chr19:41430200-41430800	Flanking Active TSS	Fetal Intestine Large	intestine
30	chr19:41430200-41433200	Active TSS	Lung	lung
31	chr19:41430400-41430600	Active TSS	Liver	Liver
32	chr19:41430400-41430600	Flanking Bivalent TSS/Enh	A549	lung
33	chr19:41430400-41430800	Enhancers	Stomach Mucosa	stomach
34	chr19:41430400-41432800	Active TSS	Fetal Intestine Small	intestine
35	chr19:41430600-41430800	Flanking Active TSS	Liver	Liver
36	chr19:41430600-41430800	Enhancers	Sigmoid Colon	Sigmoid Colon
37	chr19:41430600-41430800	Bivalent Enhancer	A549	lung
38	chr19:41430600-41430800	Enhancers	Hela-S3	cervix
39	chr19:41430600-41432600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr19:41430800-41431400	Enhancers	Duodenum Mucosa	Duodenum
41	chr19:41430800-41431600	Active TSS	Liver	Liver
42	chr19:41430800-41432800	Active TSS	Fetal Intestine Large	intestine
43	chr19:41431600-41432000	Flanking Active TSS	Liver	Liver
44	chr19:41432000-41432200	Enhancers	Liver	Liver
45	chr19:41432200-41447600	Weak transcription	Liver	Liver
46	chr19:41432400-41432600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr19:41432600-41433000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr19:41432600-41434600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr19:41432800-41433000	Flanking Active TSS	Fetal Intestine Small	intestine
50	chr19:41432800-41433200	Flanking Active TSS	Fetal Intestine Large	intestine

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