Variant report

Variant	nsv1065684
Chromosome Location	chr19:41516389-41644542
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1131)
CpG islands
(count:2812)
Chromatin interactive
region (count:17)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1131 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:41570900-41571220	K562	blood:	n/a	n/a
2	ATF1	chr19:41551132-41551364	K562	blood:	n/a	n/a
3	ATF2	chr19:41632705-41633050	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr19:41595895-41596235	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr19:41545692-41546096	K562	blood:	n/a	n/a
6	BACH1	chr19:41545740-41546031	K562	blood:	n/a	n/a
7	BACH1	chr19:41633739-41634068	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr19:41545723-41546056	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr19:41602012-41602181	K562	blood:	n/a	n/a
10	CBX3	chr19:41545744-41546043	K562	blood:	n/a	n/a
11	CBX3	chr19:41641205-41641658	K562	blood:	n/a	n/a
12	CBX3	chr19:41545730-41546088	K562	blood:	n/a	n/a
13	CBX3	chr19:41633673-41634067	K562	blood:	n/a	n/a
14	CBX3	chr19:41601607-41601944	K562	blood:	n/a	n/a
15	CEBPB	chr19:41580473-41580764	HepG2	liver:	n/a	chr19:41580633-41580644
16	CEBPB	chr19:41633758-41633806	A549	lung:	n/a	n/a
17	CEBPB	chr19:41612130-41612377	Hela-S3	cervix:	n/a	chr19:41612266-41612277
18	CEBPB	chr19:41633738-41633817	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr19:41632768-41633061	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr19:41580573-41580736	IMR90	lung:	n/a	chr19:41580633-41580644
21	CEBPB	chr19:41548015-41548148	A549	lung:	n/a	n/a
22	CEBPB	chr19:41623653-41623893	MCF-7	breast:	n/a	n/a
23	CEBPB	chr19:41630028-41630136	HepG2	liver:	n/a	n/a
24	CEBPB	chr19:41623635-41623835	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr19:41612166-41612279	H1-hESC	embryonic stem cell:	n/a	chr19:41612266-41612277
26	CEBPB	chr19:41623799-41623919	A549	lung:	n/a	n/a
27	CEBPB	chr19:41537730-41538295	MCF-7	breast:	n/a	chr19:41537946-41537958
28	CEBPB	chr19:41641877-41641888	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr19:41623786-41623841	IMR90	lung:	n/a	n/a
30	CEBPB	chr19:41612105-41612447	HepG2	liver:	n/a	chr19:41612266-41612277
31	CEBPB	chr19:41580598-41580688	H1-hESC	embryonic stem cell:	n/a	chr19:41580633-41580644
32	CEBPB	chr19:41580530-41580745	K562	blood:	n/a	chr19:41580633-41580644
33	CEBPB	chr19:41602688-41602965	A549	lung:	n/a	chr19:41602812-41602829
34	CEBPB	chr19:41602701-41602963	HepG2	liver:	n/a	chr19:41602812-41602829
35	CEBPB	chr19:41537723-41538348	MCF-7	breast:	n/a	chr19:41537946-41537958
36	CEBPB	chr19:41612093-41612457	A549	lung:	n/a	chr19:41612266-41612277
37	CEBPB	chr19:41537932-41538128	Hela-S3	cervix:	n/a	chr19:41537946-41537958
38	CEBPB	chr19:41612117-41612446	K562	blood:	n/a	chr19:41612266-41612277
39	CEBPB	chr19:41580495-41580780	A549	lung:	n/a	chr19:41580633-41580644
40	CEBPB	chr19:41580628-41580647	Hela-S3	cervix:	n/a	chr19:41580633-41580644
41	CEBPB	chr19:41559363-41559560	HepG2	liver:	n/a	n/a
42	CEBPB	chr19:41623802-41623993	K562	blood:	n/a	n/a
43	CEBPB	chr19:41573328-41573433	A549	lung:	n/a	n/a
44	CEBPB	chr19:41612098-41612450	IMR90	lung:	n/a	chr19:41612266-41612277
45	CHD2	chr19:41571045-41571167	K562	blood:	n/a	n/a
46	CHD2	chr19:41570926-41571215	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr19:41570843-41571298	K562	blood:	n/a	n/a
48	CREB1	chr19:41570905-41571266	A549	lung:	n/a	n/a
49	CREB1	chr19:41570828-41571179	HepG2	liver:	n/a	n/a
50	CREB1	chr19:41633660-41634108	A549	lung:	n/a	chr19:41633688-41633701

(count:2812 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:41618922-41618972	PrEC	prostate:	n/a
2	chr19:41601892-41601942	GM12891	blood:	n/a
3	chr19:41535072-41535122	GM12892	blood:	n/a
4	chr19:41619952-41620002	ProgFib	skin:	n/a
5	chr19:41524298-41524348	MCF10A-Er-Src	breast:	n/a
6	chr19:41601892-41601942	U87	brain:	n/a
7	chr19:41618922-41618972	PrEC	prostate:	n/a
8	chr19:41601892-41601942	GM12891	blood:	n/a
9	chr19:41535072-41535122	GM12892	blood:	n/a
10	chr19:41619952-41620002	ProgFib	skin:	n/a
11	chr19:41524298-41524348	MCF10A-Er-Src	breast:	n/a
12	chr19:41601892-41601942	U87	brain:	n/a
13	chr19:41641742-41641792	NHBE	bronchial:	n/a
14	chr19:41643199-41643249	Caco-2	colon:	n/a
15	chr19:41620211-41620261	ECC-1	luminal epithelium:	n/a
16	chr19:41634828-41634878	HRCEpiC	kidney:	n/a
17	chr19:41627236-41627286	U87	brain:	n/a
18	chr19:41640397-41640447	T-47D	breast:	n/a
19	chr19:41594746-41594796	H1-hESC	embryonic stem cell:	embryo
20	chr19:41634046-41634096	MCF10A-Er-Src	breast:	n/a
21	chr19:41642064-41642114	BE2_C	brain:	n/a
22	chr19:41640676-41640726	MCF10A-Er-Src	breast:	n/a
23	chr19:41601892-41601942	T-47D	breast:	n/a
24	chr19:41596066-41596116	NHDF-neo	bronchial:	n/a
25	chr19:41619952-41620002	Caco-2	colon:	n/a
26	chr19:41593202-41593252	HUVEC	blood vessel:	n/a
27	chr19:41627236-41627286	AoSMC	blood vessel:	n/a
28	chr19:41634046-41634096	PFSK-1	brain:	n/a
29	chr19:41531805-41531855	Hela-S3	cervix:	n/a
30	chr19:41594746-41594796	HIPEpiC	eye:	n/a
31	chr19:41593995-41594045	LNCaP	prostate:	n/a
32	chr19:41596066-41596116	HPAEpiC	pulmonary alveolar:	n/a
33	chr19:41601892-41601942	AG09309	skin:	n/a
34	chr19:41596066-41596116	GM12892	blood:	n/a
35	chr19:41642064-41642114	BJ	skin:	n/a
36	chr19:41633902-41633952	ProgFib	skin:	n/a
37	chr19:41619952-41620002	U87	brain:	n/a
38	chr19:41531634-41531684	GM12891	blood:	n/a
39	chr19:41640397-41640447	SKMC	muscle:	n/a
40	chr19:41601892-41601942	PANC-1	pancreas:	n/a
41	chr19:41630546-41630596	AG09319	gingival:	n/a
42	chr19:41531805-41531855	NHDF-neo	bronchial:	n/a
43	chr19:41633906-41633956	HNPCEpiC	eye:	n/a
44	chr19:41641847-41641897	A549	lung:	n/a
45	chr19:41596486-41596536	AoSMC	blood vessel:	n/a
46	chr19:41629018-41629068	MCF-7	breast:	n/a
47	chr19:41630511-41630561	NHDF-neo	bronchial:	n/a
48	chr19:41633906-41633956	HPAEpiC	pulmonary alveolar:	n/a
49	chr19:41640397-41640447	MCF10A-Er-Src	breast:	n/a
50	chr19:41618922-41618972	SK-N-SH	brain:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:41621979..41624352-chr19:41625905..41628342,2	K562	blood:
2	chr19:41563480..41565776-chr19:41588166..41589708,2	MCF-7	breast:
3	chr19:41563694..41565684-chr19:41568429..41571133,2	MCF-7	breast:
4	chr19:41558214..41561207-chr19:41573889..41576480,2	K562	blood:
5	chr19:41621979..41624352-chr19:41625905..41628342,2	K562	blood:
6	chr19:41633343..41635661-chr19:41766604..41769050,2	K562	blood:
7	chr19:41254906..41257408-chr19:41618440..41620283,2	MCF-7	breast:
8	chr19:41563694..41565684-chr19:41568429..41571133,2	MCF-7	breast:
9	chr19:41223179..41225407-chr19:41612527..41615194,2	MCF-7	breast:
10	chr19:41323756..41325875-chr19:41632979..41635488,2	MCF-7	breast:
11	chr19:41622398..41625038-chr19:41628718..41631460,2	MCF-7	breast:
12	chr19:41528977..41530590-chr19:41532130..41533740,2	K562	blood:
13	chr19:41631544..41633545-chr19:41769821..41772768,2	MCF-7	breast:
14	chr19:41310257..41312648-chr19:41642254..41645069,2	K562	blood:
15	chr19:41563480..41565776-chr19:41588166..41589708,2	MCF-7	breast:
16	chr19:41426562..41427465-chr19:41557958..41558773,3	MCF-7	breast:
17	chr19:41558214..41561207-chr19:41573889..41576480,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CYP2A7P1-1	chr19:41579709-41580012	NONHSAT066430
2	lnc-CYP2A7P1-2	chr19:41642278-41642471	NONHSAT066433
3	lnc-CYP2A7P1-2	chr19:41626672-41627570	NONHSAT066433

No data

Variant related genes	Relation type
CYP2G2P	TF binding region
CYP2F1	TF binding region
CYP2A13	TF binding region
ENSG00000271299	TF binding region
CYP2A7P1	TF binding region
CYP2T3P	TF binding region
CYP2G2P	CpG island
CYP2F1	CpG island
CYP2A13	CpG island
ENSG00000271299	CpG island
CYP2A7P1	CpG island
CYP2T3P	CpG island
ENSG00000077312	chromatin interactions
ENSG00000213908	chromatin interactions
ENSG00000123815	chromatin interactions
ENSG00000197446	chromatin interactions
ENSG00000269858	chromatin interactions
ENSG00000105323	chromatin interactions
ENSG00000188493	chromatin interactions

Extended variants
information (count: 4630 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:4630 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146227786	chr19:41516392-41516393	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs183506021	chr19:41516403-41516404	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561520323	chr19:41516407-41516408	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529070661	chr19:41516418-41516419	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs550421675	chr19:41516421-41516422	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs35051166	chr19:41516443-41516444	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs34027040	chr19:41516444-41516445	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs34842746	chr19:41516446-41516447	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs566429492	chr19:41516463-41516464	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs35222661	chr19:41516467-41516468	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs34083789	chr19:41516485-41516486	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs35999356	chr19:41516494-41516495	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs34566353	chr19:41516505-41516506	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs34094522	chr19:41516516-41516517	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs149000595	chr19:41516520-41516521	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs35613640	chr19:41516550-41516551	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs35005584	chr19:41516554-41516555	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs376461828	chr19:41516556-41516557	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs34223056	chr19:41516573-41516574	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568634169	chr19:41516598-41516599	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs114807742	chr19:41516603-41516604	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs557638532	chr19:41516631-41516632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556694054	chr19:41516644-41516645	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189134301	chr19:41516647-41516648	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs142978769	chr19:41516659-41516660	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs113535769	chr19:41516662-41516663	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs533785957	chr19:41516665-41516666	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555115209	chr19:41516673-41516674	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs151086735	chr19:41516694-41516695	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs11882424	chr19:41516722-41516723	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs142583125	chr19:41516784-41516785	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs146504460	chr19:41516792-41516793	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544049455	chr19:41516795-41516796	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs139175533	chr19:41516818-41516819	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs78633574	chr19:41516846-41516847	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs147028723	chr19:41516888-41516889	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs193002414	chr19:41516900-41516901	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs539170990	chr19:41516911-41516912	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185314452	chr19:41516932-41516933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138148974	chr19:41516935-41516936	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs34830389	chr19:41516946-41516947	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs536049819	chr19:41516948-41516949	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs35185769	chr19:41516951-41516952	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149525861	chr19:41516974-41516975	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181535627	chr19:41516986-41516987	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540100794	chr19:41516998-41516999	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558185524	chr19:41517050-41517051	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs566820335	chr19:41517054-41517055	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs560015360	chr19:41517061-41517062	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs533935901	chr19:41517091-41517092	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Medulloblastoma	21163964	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:698 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41507400-41529200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr19:41508000-41522400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr19:41513600-41520000	Weak transcription	Fetal Intestine Small	intestine
4	chr19:41514000-41524600	Strong transcription	Liver	Liver
5	chr19:41514400-41519200	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr19:41520000-41520200	ZNF genes & repeats	Fetal Intestine Small	intestine
7	chr19:41520200-41524400	Weak transcription	Fetal Intestine Small	intestine
8	chr19:41520600-41521800	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr19:41521200-41521800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr19:41521800-41523800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr19:41522400-41522600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr19:41522400-41522600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr19:41522400-41522800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
14	chr19:41522400-41523000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr19:41522600-41522800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr19:41523800-41524400	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr19:41524600-41531800	Weak transcription	Liver	Liver
18	chr19:41525000-41525400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
19	chr19:41525200-41525600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr19:41528400-41528600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr19:41528600-41529400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr19:41528800-41529000	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr19:41529200-41529400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
24	chr19:41529200-41529400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr19:41529400-41529600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr19:41529400-41531800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr19:41530200-41534000	Weak transcription	Right Atrium	heart
28	chr19:41531200-41531800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr19:41531400-41532000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr19:41531400-41532200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
31	chr19:41531600-41531800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
32	chr19:41531600-41531800	Bivalent Enhancer	Lung	lung
33	chr19:41531600-41532200	Bivalent Enhancer	Placenta	Placenta
34	chr19:41531600-41532400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr19:41531800-41532000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
36	chr19:41531800-41532000	Enhancers	Liver	Liver
37	chr19:41531800-41532000	Bivalent Enhancer	Colonic Mucosa	Colon
38	chr19:41531800-41532200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr19:41531800-41532200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
40	chr19:41531800-41532200	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr19:41531800-41532200	Enhancers	Pancreas	Pancrea
42	chr19:41532000-41532200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
43	chr19:41532000-41532200	Weak transcription	Liver	Liver
44	chr19:41532200-41532400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
45	chr19:41532200-41532400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
46	chr19:41532200-41536800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr19:41532200-41537000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr19:41533600-41533800	Bivalent Enhancer	Fetal Intestine Small	intestine
49	chr19:41533800-41534000	Enhancers	Fetal Intestine Small	intestine
50	chr19:41534200-41534400	Enhancers	Placenta	Placenta

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