Variant report

Variant	esv12495
Chromosome Location	chr19:18746535-18747892
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:322)
CpG islands
(count:550)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:322 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:18747519-18747929	K562	blood:	n/a	n/a
2	ATF3	chr19:18747756-18747997	K562	blood:	n/a	n/a
3	ATF3	chr19:18747762-18747941	GM12878	blood:	n/a	n/a
4	BACH1	chr19:18747805-18747960	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr19:18747309-18747344	K562	blood:	n/a	n/a
6	BHLHE40	chr19:18746864-18747605	GM12878	blood:	n/a	chr19:18747037-18747046
7	BHLHE40	chr19:18747885-18747926	K562	blood:	n/a	n/a
8	BHLHE40	chr19:18746835-18747478	K562	blood:	n/a	chr19:18747037-18747046
9	BHLHE40	chr19:18746866-18747411	HepG2	liver:	n/a	chr19:18747037-18747046
10	BRCA1	chr19:18747417-18747501	HepG2	liver:	n/a	n/a
11	BRCA1	chr19:18747315-18747432	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr19:18747093-18747690	K562	blood:	n/a	n/a
13	CCNT2	chr19:18747288-18748028	K562	blood:	n/a	chr19:18747761-18747770
14	CHD1	chr19:18747892-18747957	GM12878	blood:	n/a	n/a
15	CHD2	chr19:18747272-18747503	K562	blood:	n/a	n/a
16	CHD2	chr19:18746902-18747891	Hela-S3	cervix:	n/a	n/a
17	CREB1	chr19:18747416-18748097	H1-hESC	embryonic stem cell:	n/a	n/a
18	CREB1	chr19:18746976-18748182	K562	blood:	n/a	n/a
19	CREB1	chr19:18746769-18748180	HepG2	liver:	n/a	n/a
20	CREB1	chr19:18746990-18748208	GM12878	blood:	n/a	n/a
21	CREB1	chr19:18747642-18748063	ECC-1	luminal epithelium:	n/a	n/a
22	CREB1	chr19:18747509-18747978	A549	lung:	n/a	n/a
23	CREB1	chr19:18747541-18748205	H1-hESC	embryonic stem cell:	n/a	n/a
24	CREB1	chr19:18747530-18748171	K562	blood:	n/a	n/a
25	CTCF	chr19:18747464-18747475	Lung_OC	lung:	n/a	n/a
26	CTCF	chr19:18747302-18747605	H1-hESC	embryonic stem cell:	n/a	n/a
27	E2F4	chr19:18747454-18748058	K562	blood:	n/a	chr19:18747632-18747642
28	E2F4	chr19:18747160-18747921	MCF10A-Er-Src	breast:	n/a	chr19:18747196-18747206 chr19:18747367-18747377 chr19:18747391-18747400 chr19:18747632-18747642
29	E2F6	chr19:18747697-18747926	K562	blood:	n/a	n/a
30	E2F6	chr19:18747749-18747880	K562	blood:	n/a	n/a
31	EBF1	chr19:18746886-18747081	GM12878	blood:	n/a	n/a
32	EGR1	chr19:18746935-18747611	K562	blood:	n/a	chr19:18747390-18747400 chr19:18747104-18747117 chr19:18747392-18747405 chr19:18747161-18747171 chr19:18747129-18747142
33	EGR1	chr19:18746981-18747329	K562	blood:	n/a	chr19:18747104-18747117 chr19:18747161-18747171 chr19:18747129-18747142
34	ELF1	chr19:18747344-18747985	K562	blood:	n/a	chr19:18747754-18747766
35	ELF1	chr19:18747108-18747747	GM12878	blood:	n/a	chr19:18747110-18747122
36	ELF1	chr19:18747338-18747783	HepG2	liver:	n/a	chr19:18747754-18747766
37	ELF1	chr19:18747390-18747992	K562	blood:	n/a	chr19:18747754-18747766
38	ELK1	chr19:18747449-18747450	K562	blood:	n/a	n/a
39	ELK1	chr19:18747372-18747379	Hela-S3	cervix:	n/a	n/a
40	FOS	chr19:18747529-18747744	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr19:18747480-18747645	MCF10A-Er-Src	breast:	n/a	n/a
42	FOXP2	chr19:18747232-18747995	PFSK-1	brain:	n/a	n/a
43	GTF2F1	chr19:18747339-18747358	K562	blood:	n/a	n/a
44	GTF2F1	chr19:18747840-18747895	H1-hESC	embryonic stem cell:	n/a	n/a
45	GTF2F1	chr19:18747236-18747405	H1-hESC	embryonic stem cell:	n/a	n/a
46	HCFC1	chr19:18747322-18748050	K562	blood:	n/a	n/a
47	HCFC1	chr19:18746577-18748328	Hela-S3	cervix:	n/a	n/a
48	HEY1	chr19:18747754-18748073	K562	blood:	n/a	n/a
49	HEY1	chr19:18747747-18748106	HepG2	liver:	n/a	n/a
50	HEY1	chr19:18747764-18748007	HepG2	liver:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:18747733-18747783	PANC-1	pancreas:	n/a
2	chr19:18747733-18747783	PANC-1	pancreas:	n/a
3	chr19:18746981-18747031	HEEpiC	esophagus:	n/a
4	chr19:18746992-18747042	ProgFib	skin:	n/a
5	chr19:18747721-18747771	Caco-2	colon:	n/a
6	chr19:18746985-18747035	LNCaP	prostate:	n/a
7	chr19:18747619-18747669	GM06990	blood:	n/a
8	chr19:18747727-18747777	Jurkat	blood:	n/a
9	chr19:18746992-18747042	NT2-D1	testis:	n/a
10	chr19:18747733-18747783	GM06990	blood:	n/a
11	chr19:18747619-18747669	HCF	heart:	n/a
12	chr19:18747704-18747754	SAEC	small airway:	n/a
13	chr19:18746985-18747035	SAEC	small airway:	n/a
14	chr19:18747691-18747741	NHBE	bronchial:	n/a
15	chr19:18747721-18747771	HRE	kidney:	n/a
16	chr19:18746992-18747042	HMEC	breast:	n/a
17	chr19:18746981-18747031	GM19239	blood:	n/a
18	chr19:18746981-18747031	Caco-2	colon:	n/a
19	chr19:18747691-18747741	HPAEpiC	pulmonary alveolar:	n/a
20	chr19:18746981-18747031	AG10803	skin:	n/a
21	chr19:18746981-18747031	SK-N-SH_RA	brain:	n/a
22	chr19:18747704-18747754	HCPEpiC	choroid plexus:	n/a
23	chr19:18747727-18747777	HRPEpiC	eye:	n/a
24	chr19:18747704-18747754	GM12878	blood:	n/a
25	chr19:18747704-18747754	LNCaP	prostate:	n/a
26	chr19:18747691-18747741	LNCaP	prostate:	n/a
27	chr19:18747727-18747777	GM12878	blood:	n/a
28	chr19:18747721-18747771	NH-A	brain:	n/a
29	chr19:18746985-18747035	HEK293	kidney:	embryo
30	chr19:18747704-18747754	BJ	skin:	n/a
31	chr19:18747619-18747669	SKMC	muscle:	n/a
32	chr19:18747691-18747741	NB4	blood:	n/a
33	chr19:18747733-18747783	BE2_C	brain:	n/a
34	chr19:18747691-18747741	HEEpiC	esophagus:	n/a
35	chr19:18746985-18747035	NT2-D1	testis:	n/a
36	chr19:18746981-18747031	HL-60	blood:	n/a
37	chr19:18746992-18747042	HUVEC	blood vessel:	n/a
38	chr19:18746992-18747042	NH-A	brain:	n/a
39	chr19:18747619-18747669	GM12891	blood:	n/a
40	chr19:18746985-18747035	HMEC	breast:	n/a
41	chr19:18747721-18747771	SK-N-MC	brain:	n/a
42	chr19:18747733-18747783	NHBE	bronchial:	n/a
43	chr19:18747721-18747771	SK-N-SH_RA	brain:	n/a
44	chr19:18747727-18747777	K562	blood:	n/a
45	chr19:18747691-18747741	A549	lung:	n/a
46	chr19:18746985-18747035	HRPEpiC	eye:	n/a
47	chr19:18747721-18747771	HRPEpiC	eye:	n/a
48	chr19:18746985-18747035	NHBE	bronchial:	n/a
49	chr19:18747704-18747754	SK-N-SH_RA	brain:	n/a
50	chr19:18746981-18747031	NH-A	brain:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:18698708..18701515-chr19:18746316..18749182,4	MCF-7	breast:
2	chr19:18698512..18700358-chr19:18745222..18750244,4	K562	blood:
3	chr19:18700524..18703188-chr19:18747828..18749371,2	K562	blood:
4	chr19:18699138..18701400-chr19:18744196..18746923,2	K562	blood:
5	chr19:18738729..18743227-chr19:18745299..18749316,6	K562	blood:
6	chr19:18630375..18633112-chr19:18747617..18750132,3	K562	blood:
7	chr19:18716807..18719687-chr19:18745756..18748857,3	K562	blood:
8	chr19:18739642..18741715-chr19:18744659..18746767,2	MCF-7	breast:
9	chr19:18703681..18707981-chr19:18746387..18750076,5	K562	blood:
10	chr19:18717575..18719687-chr19:18746806..18748857,2	K562	blood:
11	chr19:18681104..18684544-chr19:18745683..18749906,4	K562	blood:
12	chr19:18744815..18748522-chr19:18792822..18794594,3	K562	blood:
13	chr19:18746749..18750617-chr19:18752436..18756057,4	K562	blood:
14	chr19:18740493..18743219-chr19:18745834..18748100,2	K562	blood:
15	chr19:18744967..18748846-chr19:18753096..18757449,4	MCF-7	breast:
16	chr19:18704018..18706684-chr19:18745467..18747163,2	MCF-7	breast:
17	chr19:18747079..18749227-chr19:18751650..18755741,5	MCF-7	breast:
18	chr19:18553947..18555891-chr19:18746913..18749059,2	K562	blood:
19	chr19:18745231..18747115-chr19:18793241..18795774,2	MCF-7	breast:
20	chr19:18681409..18685264-chr19:18744559..18747664,3	MCF-7	breast:

No data

Variant related genes	Relation type
KLHL26	TF binding region
RN7SL155P	TF binding region
KLHL26	CpG island
RN7SL155P	CpG island
ENSG00000167487	chromatin interactions
ENSG00000006016	chromatin interactions
ENSG00000221983	chromatin interactions
ENSG00000105662	chromatin interactions
ENSG00000256989	chromatin interactions
ENSG00000105696	chromatin interactions
ENSG00000006015	chromatin interactions
ENSG00000105656	chromatin interactions
ENSG00000263490	chromatin interactions

Extended variants
information (count: 41 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:41 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565286805	chr19:18746542-18746543	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs534314048	chr19:18746547-18746548	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs547920452	chr19:18746548-18746549	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs78041499	chr19:18746576-18746577	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs1991017	chr19:18746593-18746594	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs143014528	chr19:18746626-18746627	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs539314104	chr19:18746668-18746669	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
8	rs558998532	chr19:18746771-18746772	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
9	rs185391903	chr19:18746831-18746832	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
10	rs541430267	chr19:18746846-18746847	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs561404774	chr19:18746968-18746969	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
12	rs574808794	chr19:18747046-18747047	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
13	rs117009988	chr19:18747048-18747049	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
14	rs563688034	chr19:18747120-18747121	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
15	rs147445774	chr19:18747143-18747144	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
16	rs532841171	chr19:18747161-18747162	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
17	rs77267035	chr19:18747168-18747169	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
18	rs559608926	chr19:18747180-18747181	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
19	rs528108258	chr19:18747187-18747188	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
20	rs547760785	chr19:18747199-18747200	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
21	rs567837959	chr19:18747232-18747233	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
22	rs75473975	chr19:18747244-18747245	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
23	rs550761728	chr19:18747264-18747265	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
24	rs182920776	chr19:18747317-18747318	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
25	rs539619237	chr19:18747334-18747335	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
26	rs553347144	chr19:18747345-18747346	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
27	rs573160965	chr19:18747402-18747403	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
28	rs75059778	chr19:18747428-18747429	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
29	rs554965621	chr19:18747473-18747474	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
30	rs187514210	chr19:18747565-18747566	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
31	rs3764628	chr19:18747605-18747606	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
32	rs374110145	chr19:18747649-18747650	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
33	rs563797974	chr19:18747692-18747693	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
34	rs3764627	chr19:18747696-18747697	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs535094615	chr19:18747737-18747738	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
36	rs559646815	chr19:18747743-18747744	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
37	rs528733615	chr19:18747784-18747785	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
38	rs546095738	chr19:18747792-18747793	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
39	rs555610513	chr19:18747832-18747833	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
40	rs561485335	chr19:18747858-18747859	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
41	rs530634471	chr19:18747886-18747887	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Follicular lymphoma	20505157	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	20179077	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Lung cancer	17297452	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Chordoma	18071362	CNVD
Ewing''s sarcoma	21437220	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
Urothelial carcinoma	21177765	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Basal cell lymphoma	21115979	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Medullary thyroid carcinoma	18765511	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
Mycobacterial infection	18421352	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute monocytic leukemia	16498392	CNVD
Lung cancer	18438408	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Liver carcinoma	19366792	CNVD
Colorectal cancer	19455253	CNVD
Lujan-Fryns syndrom	21521776	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Cancer	17440070	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:331 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18725600-18747200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr19:18729400-18747200	Weak transcription	Brain Angular Gyrus	brain
3	chr19:18740600-18746600	Weak transcription	Fetal Brain Female	brain
4	chr19:18740800-18746600	Weak transcription	Brain Anterior Caudate	brain
5	chr19:18740800-18746600	Weak transcription	Brain Substantia Nigra	brain
6	chr19:18740800-18747200	Weak transcription	Brain Hippocampus Middle	brain
7	chr19:18740800-18747200	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr19:18741200-18746800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr19:18741200-18747200	Weak transcription	Adipose Nuclei	Adipose
10	chr19:18745200-18746600	Bivalent Enhancer	Fetal Muscle Leg	muscle
11	chr19:18745600-18746600	Enhancers	Duodenum Mucosa	Duodenum
12	chr19:18745600-18746600	Enhancers	Esophagus	oesophagus
13	chr19:18745600-18746600	Enhancers	Fetal Lung	lung
14	chr19:18745600-18746600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
15	chr19:18745600-18746600	Bivalent Enhancer	Placenta	Placenta
16	chr19:18745600-18746800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr19:18745600-18746800	Enhancers	Right Ventricle	heart
18	chr19:18745600-18746800	Flanking Active TSS	HepG2	liver
19	chr19:18745600-18747000	Enhancers	Primary T helper cells PMA-I stimulated	--
20	chr19:18745600-18747200	Enhancers	Primary T cells fromperipheralblood	blood
21	chr19:18745600-18747200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr19:18745600-18747200	Enhancers	Rectal Mucosa Donor 31	rectum
23	chr19:18745600-18747200	Enhancers	NHEK	skin
24	chr19:18745600-18747800	Enhancers	Fetal Brain Male	brain
25	chr19:18745800-18746600	Enhancers	Right Atrium	heart
26	chr19:18745800-18746800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr19:18745800-18746800	Enhancers	Primary hematopoietic stem cells	blood
28	chr19:18745800-18747200	Enhancers	Primary T cells from cord blood	blood
29	chr19:18745800-18747200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
30	chr19:18745800-18747200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
31	chr19:18745800-18747400	Enhancers	Stomach Mucosa	stomach
32	chr19:18746000-18746600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
33	chr19:18746000-18746600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr19:18746000-18746600	Enhancers	Primary T helper cells fromperipheralblood	blood
35	chr19:18746000-18746600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr19:18746000-18746600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr19:18746000-18746600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr19:18746000-18746600	Enhancers	Gastric	stomach
39	chr19:18746000-18746600	Enhancers	Rectal Mucosa Donor 29	rectum
40	chr19:18746000-18746800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
41	chr19:18746000-18746800	Enhancers	Brain Germinal Matrix	brain
42	chr19:18746000-18746800	Enhancers	Thymus	Thymus
43	chr19:18746000-18747000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr19:18746000-18747000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr19:18746000-18747000	Enhancers	Primary T helper naive cells from peripheral blood	blood
46	chr19:18746000-18747200	Enhancers	Primary B cells from peripheral blood	blood
47	chr19:18746000-18747200	Enhancers	Primary T killer memory cells from peripheral blood	blood
48	chr19:18746000-18747200	Enhancers	Fetal Intestine Small	intestine
49	chr19:18746000-18747200	Weak transcription	Left Ventricle	heart
50	chr19:18746000-18747200	Weak transcription	Lung	lung

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