Variant report

Variant	nsv578759
Chromosome Location	chr19:18747006-18747845
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:314)
CpG islands
(count:549)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:314 , 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	chr19:18746866-18747411	HepG2	liver:	n/a	chr19:18747037-18747046
7	BHLHE40	chr19:18746864-18747605	GM12878	blood:	n/a	chr19:18747037-18747046
8	BHLHE40	chr19:18746835-18747478	K562	blood:	n/a	chr19:18747037-18747046
9	BRCA1	chr19:18747417-18747501	HepG2	liver:	n/a	n/a
10	BRCA1	chr19:18747315-18747432	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr19:18747093-18747690	K562	blood:	n/a	n/a
12	CCNT2	chr19:18747288-18748028	K562	blood:	n/a	chr19:18747761-18747770
13	CHD2	chr19:18747272-18747503	K562	blood:	n/a	n/a
14	CHD2	chr19:18746902-18747891	Hela-S3	cervix:	n/a	n/a
15	CREB1	chr19:18747416-18748097	H1-hESC	embryonic stem cell:	n/a	n/a
16	CREB1	chr19:18746990-18748208	GM12878	blood:	n/a	n/a
17	CREB1	chr19:18747509-18747978	A549	lung:	n/a	n/a
18	CREB1	chr19:18747541-18748205	H1-hESC	embryonic stem cell:	n/a	n/a
19	CREB1	chr19:18747530-18748171	K562	blood:	n/a	n/a
20	CREB1	chr19:18746976-18748182	K562	blood:	n/a	n/a
21	CREB1	chr19:18746769-18748180	HepG2	liver:	n/a	n/a
22	CREB1	chr19:18747642-18748063	ECC-1	luminal epithelium:	n/a	n/a
23	CTCF	chr19:18747302-18747605	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr19:18747464-18747475	Lung_OC	lung:	n/a	n/a
25	E2F4	chr19:18747454-18748058	K562	blood:	n/a	chr19:18747632-18747642
26	E2F4	chr19:18747160-18747921	MCF10A-Er-Src	breast:	n/a	chr19:18747196-18747206 chr19:18747367-18747377 chr19:18747391-18747400 chr19:18747632-18747642
27	E2F6	chr19:18747749-18747880	K562	blood:	n/a	n/a
28	E2F6	chr19:18747697-18747926	K562	blood:	n/a	n/a
29	EBF1	chr19:18746886-18747081	GM12878	blood:	n/a	n/a
30	EGR1	chr19:18746935-18747611	K562	blood:	n/a	chr19:18747390-18747400 chr19:18747104-18747117 chr19:18747392-18747405 chr19:18747161-18747171 chr19:18747129-18747142
31	EGR1	chr19:18746981-18747329	K562	blood:	n/a	chr19:18747104-18747117 chr19:18747161-18747171 chr19:18747129-18747142
32	ELF1	chr19:18747390-18747992	K562	blood:	n/a	chr19:18747754-18747766
33	ELF1	chr19:18747108-18747747	GM12878	blood:	n/a	chr19:18747110-18747122
34	ELF1	chr19:18747338-18747783	HepG2	liver:	n/a	chr19:18747754-18747766
35	ELF1	chr19:18747344-18747985	K562	blood:	n/a	chr19:18747754-18747766
36	ELK1	chr19:18747372-18747379	Hela-S3	cervix:	n/a	n/a
37	ELK1	chr19:18747449-18747450	K562	blood:	n/a	n/a
38	FOS	chr19:18747529-18747744	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr19:18747480-18747645	MCF10A-Er-Src	breast:	n/a	n/a
40	FOXP2	chr19:18747232-18747995	PFSK-1	brain:	n/a	n/a
41	GTF2F1	chr19:18747840-18747895	H1-hESC	embryonic stem cell:	n/a	n/a
42	GTF2F1	chr19:18747339-18747358	K562	blood:	n/a	n/a
43	GTF2F1	chr19:18747236-18747405	H1-hESC	embryonic stem cell:	n/a	n/a
44	HCFC1	chr19:18747322-18748050	K562	blood:	n/a	n/a
45	HCFC1	chr19:18746577-18748328	Hela-S3	cervix:	n/a	n/a
46	HEY1	chr19:18747755-18748094	K562	blood:	n/a	n/a
47	HEY1	chr19:18747754-18748073	K562	blood:	n/a	n/a
48	HEY1	chr19:18747747-18748106	HepG2	liver:	n/a	n/a
49	HEY1	chr19:18747764-18748007	HepG2	liver:	n/a	n/a
50	HMGN3	chr19:18747335-18748066	K562	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:18746992-18747042	NHBE	bronchial:	n/a
2	chr19:18747721-18747771	NHBE	bronchial:	n/a
3	chr19:18746992-18747042	GM19239	blood:	n/a
4	chr19:18747619-18747669	HCF	heart:	n/a
5	chr19:18747619-18747669	AG10803	skin:	n/a
6	chr19:18747691-18747741	HEEpiC	esophagus:	n/a
7	chr19:18746985-18747035	GM12892	blood:	n/a
8	chr19:18747619-18747669	PrEC	prostate:	n/a
9	chr19:18747733-18747783	GM12891	blood:	n/a
10	chr19:18746992-18747042	NT2-D1	testis:	n/a
11	chr19:18746981-18747031	HCPEpiC	choroid plexus:	n/a
12	chr19:18746992-18747042	SK-N-SH	brain:	n/a
13	chr19:18747721-18747771	HAEpiC	amniotic membrane:	n/a
14	chr19:18746981-18747031	NT2-D1	testis:	n/a
15	chr19:18747704-18747754	HCPEpiC	choroid plexus:	n/a
16	chr19:18747691-18747741	H1-hESC	embryonic stem cell:	embryo
17	chr19:18746992-18747042	RPTEC	kidney:	n/a
18	chr19:18746992-18747042	H1-hESC	embryonic stem cell:	embryo
19	chr19:18747704-18747754	MCF10A-Er-Src	breast:	n/a
20	chr19:18747727-18747777	Jurkat	blood:	n/a
21	chr19:18746981-18747031	IMR90	lung:	fetal
22	chr19:18746992-18747042	IMR90	lung:	fetal
23	chr19:18747727-18747777	Hela-S3	cervix:	n/a
24	chr19:18746992-18747042	ECC-1	luminal epithelium:	n/a
25	chr19:18747691-18747741	HepG2	liver:	n/a
26	chr19:18747691-18747741	PANC-1	pancreas:	n/a
27	chr19:18747727-18747777	SK-N-SH_RA	brain:	n/a
28	chr19:18746985-18747035	HCT-116	colon:	n/a
29	chr19:18747691-18747741	PrEC	prostate:	n/a
30	chr19:18746985-18747035	SK-N-MC	brain:	n/a
31	chr19:18747733-18747783	AG04449	skin:	fetal
32	chr19:18747704-18747754	MCF-7	breast:	n/a
33	chr19:18747727-18747777	AG04449	skin:	fetal
34	chr19:18747704-18747754	HCF	heart:	n/a
35	chr19:18747704-18747754	HMEC	breast:	n/a
36	chr19:18747691-18747741	NT2-D1	testis:	n/a
37	chr19:18747704-18747754	CMK	blood:	n/a
38	chr19:18746992-18747042	SK-N-MC	brain:	n/a
39	chr19:18747721-18747771	HRPEpiC	eye:	n/a
40	chr19:18747704-18747754	SK-N-MC	brain:	n/a
41	chr19:18746981-18747031	Jurkat	blood:	n/a
42	chr19:18746985-18747035	HEEpiC	esophagus:	n/a
43	chr19:18746981-18747031	ProgFib	skin:	n/a
44	chr19:18747704-18747754	SKMC	muscle:	n/a
45	chr19:18747733-18747783	NHBE	bronchial:	n/a
46	chr19:18746981-18747031	CMK	blood:	n/a
47	chr19:18746992-18747042	GM12892	blood:	n/a
48	chr19:18746992-18747042	NB4	blood:	n/a
49	chr19:18747704-18747754	HL-60	blood:	n/a
50	chr19:18747733-18747783	HL-60	blood:	n/a

(count:18 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 28 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	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
26	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
27	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
28	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

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:257 , 50 per page) page: 1 2 3 4 5 6

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	chr19:18740800-18747200	Weak transcription	Brain Hippocampus Middle	brain
4	chr19:18740800-18747200	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr19:18741200-18747200	Weak transcription	Adipose Nuclei	Adipose
6	chr19:18745600-18747200	Enhancers	Primary T cells fromperipheralblood	blood
7	chr19:18745600-18747200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr19:18745600-18747200	Enhancers	Rectal Mucosa Donor 31	rectum
9	chr19:18745600-18747200	Enhancers	NHEK	skin
10	chr19:18745600-18747800	Enhancers	Fetal Brain Male	brain
11	chr19:18745800-18747200	Enhancers	Primary T cells from cord blood	blood
12	chr19:18745800-18747200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
13	chr19:18745800-18747200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
14	chr19:18745800-18747400	Enhancers	Stomach Mucosa	stomach
15	chr19:18746000-18747200	Enhancers	Primary B cells from peripheral blood	blood
16	chr19:18746000-18747200	Enhancers	Primary T killer memory cells from peripheral blood	blood
17	chr19:18746000-18747200	Enhancers	Fetal Intestine Small	intestine
18	chr19:18746000-18747200	Weak transcription	Left Ventricle	heart
19	chr19:18746000-18747200	Weak transcription	Lung	lung
20	chr19:18746200-18747200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr19:18746200-18747200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
22	chr19:18746200-18747200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr19:18746200-18747200	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr19:18746200-18747200	Enhancers	Fetal Thymus	thymus
25	chr19:18746200-18747200	Enhancers	Pancreas	Pancrea
26	chr19:18746200-18747200	Enhancers	Small Intestine	intestine
27	chr19:18746200-18747200	Enhancers	NHDF-Ad	bronchial
28	chr19:18746200-18749000	Enhancers	Fetal Heart	heart
29	chr19:18746400-18747200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr19:18746400-18747200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr19:18746400-18747200	Weak transcription	Brain Cingulate Gyrus	brain
32	chr19:18746400-18747200	Enhancers	Fetal Intestine Large	intestine
33	chr19:18746400-18747200	Enhancers	Spleen	Spleen
34	chr19:18746600-18747200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr19:18746600-18747200	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr19:18746600-18747200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr19:18746600-18747200	Weak transcription	Duodenum Mucosa	Duodenum
38	chr19:18746600-18747200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr19:18746600-18747200	Weak transcription	Fetal Lung	lung
40	chr19:18746600-18747200	Enhancers	Fetal Muscle Leg	muscle
41	chr19:18746600-18747200	Enhancers	Placenta	Placenta
42	chr19:18746600-18747200	Weak transcription	Gastric	stomach
43	chr19:18746600-18747600	Flanking Active TSS	Dnd41	blood
44	chr19:18746600-18748000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr19:18746600-18748600	Active TSS	iPS-15b Cell Line	embryonic stem cell
46	chr19:18746600-18748800	Active TSS	A549	lung
47	chr19:18746800-18747200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr19:18746800-18747200	Enhancers	Primary B cells from cord blood	blood
49	chr19:18746800-18747200	Active TSS	Primary T helper naive cells fromperipheralblood	blood
50	chr19:18746800-18747200	Active TSS	Primary T helper cells fromperipheralblood	blood

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