Variant report

Variant	esv3375469
Chromosome Location	chr19:55671705-55672069
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:398)
CpG islands
(count:61)
Chromatin interactive
region (count:20)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:55671943-55672252	K562	blood:	n/a	n/a
2	ATF3	chr19:55671858-55672277	K562	blood:	n/a	chr19:55672187-55672196
3	BACH1	chr19:55671866-55672635	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr19:55671771-55672310	A549	lung:	n/a	n/a
5	BHLHE40	chr19:55671904-55672241	GM12878	blood:	n/a	n/a
6	BHLHE40	chr19:55671851-55672266	K562	blood:	n/a	n/a
7	BRCA1	chr19:55671889-55672277	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr19:55671931-55672094	GM12878	blood:	n/a	n/a
9	BRCA1	chr19:55672043-55672137	HepG2	liver:	n/a	n/a
10	BRCA1	chr19:55671941-55672211	H1-hESC	embryonic stem cell:	n/a	n/a
11	CBX3	chr19:55671767-55672356	K562	blood:	n/a	n/a
12	CCNT2	chr19:55671910-55672510	K562	blood:	n/a	n/a
13	CEBPB	chr19:55671995-55672209	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD1	chr19:55672039-55672188	GM12878	blood:	n/a	n/a
15	CHD2	chr19:55671911-55672297	Hela-S3	cervix:	n/a	n/a
16	CHD2	chr19:55672061-55672202	GM12878	blood:	n/a	n/a
17	CHD2	chr19:55671926-55672255	H1-hESC	embryonic stem cell:	n/a	n/a
18	CREB1	chr19:55671850-55672369	H1-hESC	embryonic stem cell:	n/a	n/a
19	CREB1	chr19:55671860-55672365	K562	blood:	n/a	n/a
20	CREB1	chr19:55671898-55672639	H1-hESC	embryonic stem cell:	n/a	n/a
21	CREB1	chr19:55671875-55672354	GM12878	blood:	n/a	n/a
22	CREB1	chr19:55671863-55672317	A549	lung:	n/a	n/a
23	CREB1	chr19:55671837-55672271	HepG2	liver:	n/a	n/a
24	CREB1	chr19:55671825-55672367	HepG2	liver:	n/a	n/a
25	CREB1	chr19:55671887-55672189	A549	lung:	n/a	n/a
26	CTCF	chr19:55671926-55672264	MCF-7	breast:	n/a	n/a
27	CTCF	chr19:55671900-55672257	T-47D	breast:	n/a	n/a
28	CTCF	chr19:55671911-55672313	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr19:55672000-55672150	MCF-7	breast:	n/a	n/a
30	CTCF	chr19:55671980-55672130	GM12869	blood:	n/a	n/a
31	CTCF	chr19:55672020-55672170	GM12865	blood:	n/a	n/a
32	CTCF	chr19:55671815-55672241	HepG2	liver:	n/a	n/a
33	CTCF	chr19:55671956-55672232	GM10248	blood:	n/a	n/a
34	CTCF	chr19:55672020-55672170	AG04449	skin:	n/a	n/a
35	CTCF	chr19:55671856-55672277	A549	lung:	n/a	n/a
36	CTCF	chr19:55671940-55672210	HCM	heart:	n/a	n/a
37	CTCF	chr19:55671669-55672417	HCT-116	colon:	n/a	n/a
38	CTCF	chr19:55671960-55672110	NB4	blood:	n/a	n/a
39	CTCF	chr19:55671939-55672236	A549	lung:	n/a	n/a
40	CTCF	chr19:55672060-55672210	GM12801	blood:	n/a	n/a
41	CTCF	chr19:55671968-55672233	Pancreas_OC	pancreas:	n/a	n/a
42	CTCF	chr19:55671947-55672222	ProgFib	skin:	n/a	n/a
43	CTCF	chr19:55672000-55672150	HVMF	connective:	n/a	n/a
44	CTCF	chr19:55672000-55672150	SAEC	small airway:	n/a	n/a
45	CTCF	chr19:55672020-55672170	HMEC	breast:	n/a	n/a
46	CTCF	chr19:55671980-55672130	HFF-Myc	foreskin:	n/a	n/a
47	CTCF	chr19:55671980-55672130	MCF-7	breast:	n/a	n/a
48	CTCF	chr19:55672000-55672150	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr19:55672000-55672150	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr19:55672000-55672150	HPF	lung:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:55672036-55672086	SK-N-SH	brain:	n/a
2	chr19:55672036-55672086	HUVEC	blood vessel:	n/a
3	chr19:55672036-55672086	HCT-116	colon:	n/a
4	chr19:55672036-55672086	RPTEC	kidney:	n/a
5	chr19:55672036-55672086	HepG2	liver:	n/a
6	chr19:55672036-55672086	NHBE	bronchial:	n/a
7	chr19:55672036-55672086	GM12892	blood:	n/a
8	chr19:55672036-55672086	HNPCEpiC	eye:	n/a
9	chr19:55672036-55672086	Jurkat	blood:	n/a
10	chr19:55672036-55672086	Hepatocyte	liver:	n/a
11	chr19:55672036-55672086	HPAEpiC	pulmonary alveolar:	n/a
12	chr19:55672036-55672086	A549	lung:	n/a
13	chr19:55672036-55672086	MCF10A-Er-Src	breast:	n/a
14	chr19:55672036-55672086	NH-A	brain:	n/a
15	chr19:55672036-55672086	AG09319	gingival:	n/a
16	chr19:55672036-55672086	SK-N-MC	brain:	n/a
17	chr19:55672036-55672086	ECC-1	luminal epithelium:	n/a
18	chr19:55672036-55672086	HEK293	kidney:	embryo
19	chr19:55672036-55672086	NB4	blood:	n/a
20	chr19:55672036-55672086	CMK	blood:	n/a
21	chr19:55672036-55672086	GM06990	blood:	n/a
22	chr19:55672036-55672086	PFSK-1	brain:	n/a
23	chr19:55672036-55672086	NHDF-neo	bronchial:	n/a
24	chr19:55672036-55672086	T-47D	breast:	n/a
25	chr19:55672036-55672086	HEEpiC	esophagus:	n/a
26	chr19:55672036-55672086	HL-60	blood:	n/a
27	chr19:55672036-55672086	LNCaP	prostate:	n/a
28	chr19:55672036-55672086	HRE	kidney:	n/a
29	chr19:55672036-55672086	BE2_C	brain:	n/a
30	chr19:55672036-55672086	AG04450	lung:	fetal
31	chr19:55672036-55672086	NT2-D1	testis:	n/a
32	chr19:55672036-55672086	ovcar-3	ovarian:	n/a
33	chr19:55672036-55672086	HRCEpiC	kidney:	n/a
34	chr19:55672036-55672086	HCPEpiC	choroid plexus:	n/a
35	chr19:55672036-55672086	Hela-S3	cervix:	n/a
36	chr19:55672036-55672086	AG10803	skin:	n/a
37	chr19:55672036-55672086	AoSMC	blood vessel:	n/a
38	chr19:55672036-55672086	GM12891	blood:	n/a
39	chr19:55672036-55672086	MCF-7	breast:	n/a
40	chr19:55672036-55672086	H1-hESC	embryonic stem cell:	embryo
41	chr19:55672036-55672086	SKMC	muscle:	n/a
42	chr19:55672036-55672086	GM12878	blood:	n/a
43	chr19:55672036-55672086	Caco-2	colon:	n/a
44	chr19:55672036-55672086	SK-N-SH_RA	brain:	n/a
45	chr19:55672036-55672086	HAEpiC	amniotic membrane:	n/a
46	chr19:55672036-55672086	HRPEpiC	eye:	n/a
47	chr19:55672036-55672086	BJ	skin:	n/a
48	chr19:55672036-55672086	HCM	heart:	n/a
49	chr19:55672036-55672086	U87	brain:	n/a
50	chr19:55672036-55672086	ProgFib	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:55652274..55653243-chr19:55671651..55672648,4	K562	blood:
2	chr19:55656783..55658511-chr19:55670096..55672623,2	MCF-7	breast:
3	chr19:55657720..55659447-chr19:55670409..55672561,2	MCF-7	breast:
4	chr19:55669654..55671920-chr19:55893818..55896729,2	MCF-7	breast:
5	chr19:55598098..55602192-chr19:55668353..55672028,4	K562	blood:
6	chr19:55670813..55674787-chr19:55917654..55919984,3	MCF-7	breast:
7	chr19:55670803..55672973-chr19:55678461..55680015,2	MCF-7	breast:
8	chr19:55669739..55671839-chr19:55895942..55898733,2	K562	blood:
9	chr19:55657176..55657861-chr19:55671612..55672279,3	MCF-7	breast:
10	chr19:55573018..55574580-chr19:55668896..55671784,2	K562	blood:
11	chr19:55656068..55658188-chr19:55669727..55672257,4	K562	blood:
12	chr19:55668909..55673851-chr19:55684249..55689420,6	K562	blood:
13	chr19:55650102..55652468-chr19:55670117..55672433,2	K562	blood:
14	chr19:55669904..55673815-chr19:55917688..55921815,5	K562	blood:
15	chr19:55590282..55593983-chr19:55668450..55672239,5	K562	blood:
16	chr19:55669094..55672573-chr19:55676633..55678240,3	K562	blood:
17	chr19:55657215..55657931-chr19:55671632..55672517,3	K562	blood:
18	chr19:55670339..55672194-chr19:55895106..55898791,3	K562	blood:
19	chr19:55627388..55629698-chr19:55672061..55673602,2	K562	blood:
20	chr19:55579852..55582710-chr19:55671936..55674879,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EPS8L1-2	chr19:55671860-55672582	NONHSAT067999
2	lnc-EPS8L1-2	chr19:55671860-55672582	NONHSAT067998

No data

Variant related genes	Relation type
ENSG00000267110	TF binding region
TNNI3	TF binding region
DNAAF3	TF binding region
ENSG00000267110	CpG island
TNNI3	CpG island
DNAAF3	CpG island
ENSG00000131037	chromatin interactions
ENSG00000167646	chromatin interactions
ENSG00000108106	chromatin interactions
ENSG00000129990	chromatin interactions
ENSG00000108107	chromatin interactions
ENSG00000160439	chromatin interactions
ENSG00000105048	chromatin interactions
ENSG00000233493	chromatin interactions
ENSG00000125503	chromatin interactions
ENSG00000239137	chromatin interactions

Extended variants
information (count: 22 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571980117	chr19:55671714-55671715	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
2	rs77353455	chr19:55671721-55671722	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
3	rs73066627	chr19:55671730-55671731	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs577759396	chr19:55671782-55671783	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
5	rs139659116	chr19:55671801-55671802	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
6	rs569446859	chr19:55671838-55671839	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs374587086	chr19:55671950-55671951	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
8	rs150324242	chr19:55671974-55671975	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
9	rs6146559	chr19:55671990-55671991	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
10	rs542851818	chr19:55671992-55671993	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
11	rs113445842	chr19:55672007-55672008	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
12	rs370282533	chr19:55672012-55672013	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
13	rs373649217	chr19:55672024-55672025	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
14	rs543007128	chr19:55672025-55672026	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
15	rs560113507	chr19:55672039-55672040	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
16	rs202056577	chr19:55672051-55672052	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
17	rs890871	chr19:55672055-55672056	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs552015501	chr19:55672057-55672058	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
19	rs571791610	chr19:55672059-55672060	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
20	rs7508641	chr19:55672065-55672066	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
21	rs371092262	chr19:55672066-55672067	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
22	rs545243133	chr19:55672067-55672068	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	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
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD
Glioblastoma multiforme	17002787	CNVD
Cervical cancer	21062161	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	16573809	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Breast cancer	20459607	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Alzheimer''s disease	22166940	CNVD
Heart disease	21282601	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Glioblastoma multiforme	21922591	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Lung squamous cell carcinoma	20842114	CNVD
Lung cancer	21203850	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:80 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:55668600-55672000	Weak transcription	Pancreas	Pancrea
2	chr19:55669000-55672000	Weak transcription	Spleen	Spleen
3	chr19:55669000-55672800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
4	chr19:55669200-55672200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr19:55669200-55672800	Enhancers	Fetal Heart	heart
6	chr19:55669600-55672400	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr19:55669600-55673400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
8	chr19:55669800-55672000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr19:55669800-55672400	Enhancers	A549	lung
10	chr19:55670000-55672000	Flanking Active TSS	K562	blood
11	chr19:55670000-55672200	Flanking Active TSS	Hela-S3	cervix
12	chr19:55670000-55672400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr19:55670200-55671800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr19:55670200-55671800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr19:55670200-55672000	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr19:55670200-55672000	Enhancers	Primary hematopoietic stem cells	blood
17	chr19:55670400-55671800	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr19:55670400-55671800	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr19:55670400-55671800	Enhancers	HSMMtube	muscle
20	chr19:55670400-55672000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr19:55670400-55672000	Enhancers	HMEC	breast
22	chr19:55670400-55672000	Flanking Active TSS	NHEK	skin
23	chr19:55670400-55672200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
24	chr19:55670400-55672400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr19:55670400-55672400	Enhancers	Placenta Amnion	Placenta Amnion
26	chr19:55670600-55671800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr19:55670600-55671800	Enhancers	HSMM	muscle
28	chr19:55670600-55672200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr19:55670600-55672200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr19:55670800-55672000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
31	chr19:55670800-55673800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
32	chr19:55671000-55673000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr19:55671400-55671800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr19:55671400-55671800	Enhancers	Esophagus	oesophagus
35	chr19:55671400-55672600	Bivalent Enhancer	Fetal Muscle Leg	muscle
36	chr19:55671600-55671800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
37	chr19:55671600-55671800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr19:55671600-55671800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
39	chr19:55671600-55671800	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
40	chr19:55671600-55671800	Flanking Active TSS	Left Ventricle	heart
41	chr19:55671600-55671800	Bivalent Enhancer	NHDF-Ad	bronchial
42	chr19:55671600-55671800	Bivalent Enhancer	NHLF	lung
43	chr19:55671600-55672000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
44	chr19:55671600-55672000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
45	chr19:55671600-55672200	Enhancers	H9 Cell Line	embryonic stem cell
46	chr19:55671600-55672200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr19:55671600-55672200	Bivalent Enhancer	Fetal Thymus	thymus
48	chr19:55671600-55672200	Enhancers	Right Ventricle	heart
49	chr19:55671600-55672400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr19:55671600-55672600	Bivalent Enhancer	Stomach Smooth Muscle	stomach

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