Variant report

Variant	esv1829773
Chromosome Location	chr19:52137652-52150859
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:282)
CpG islands
(count:427)
Chromatin interactive
region (count:11)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:282 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:52140651-52140961	K562	blood:	n/a	n/a
2	BATF	chr19:52149947-52150214	GM12878	blood:	n/a	n/a
3	BCL11A	chr19:52149937-52150305	GM12878	blood:	n/a	n/a
4	BHLHE40	chr19:52147812-52147863	K562	blood:	n/a	n/a
5	BHLHE40	chr19:52150088-52150405	K562	blood:	n/a	chr19:52150169-52150178 chr19:52150169-52150178
6	BHLHE40	chr19:52150049-52150408	GM12878	blood:	n/a	chr19:52150169-52150178 chr19:52150169-52150178
7	CBX3	chr19:52140579-52140964	K562	blood:	n/a	n/a
8	CBX3	chr19:52140595-52141003	K562	blood:	n/a	n/a
9	CEBPB	chr19:52144983-52145193	IMR90	lung:	n/a	chr19:52145111-52145122
10	CEBPB	chr19:52144962-52145257	HepG2	liver:	n/a	chr19:52145111-52145122
11	CEBPB	chr19:52144942-52145259	A549	lung:	n/a	chr19:52145111-52145122
12	CEBPB	chr19:52145000-52145199	K562	blood:	n/a	chr19:52145111-52145122
13	CTCF	chr19:52140720-52140870	NHDF-neo	bronchial:	n/a	n/a
14	CTCF	chr19:52141100-52141102	HUVEC	blood vessel:	n/a	n/a
15	CTCF	chr19:52147697-52147711	K562	blood:	n/a	n/a
16	CTCF	chr19:52140720-52140870	BE2_C	brain:	n/a	n/a
17	CTCF	chr19:52140720-52140870	GM12875	blood:	n/a	n/a
18	CTCF	chr19:52140740-52140890	RPTEC	kidney:	n/a	n/a
19	CTCF	chr19:52140740-52140890	HRPEpiC	eye:	n/a	n/a
20	CTCF	chr19:52140680-52140830	AG04450	lung:	n/a	n/a
21	CTCF	chr19:52140860-52141010	HAc	cerebellar:	n/a	n/a
22	CTCF	chr19:52140700-52140850	MCF-7	breast:	n/a	n/a
23	CTCF	chr19:52140740-52140890	GM12874	blood:	n/a	n/a
24	CTCF	chr19:52140800-52140950	GM12872	blood:	n/a	n/a
25	CTCF	chr19:52140810-52140933	GM19240	blood:	n/a	n/a
26	CTCF	chr19:52140840-52140990	A549	lung:	n/a	n/a
27	CTCF	chr19:52140700-52140850	AG10803	skin:	n/a	n/a
28	CTCF	chr19:52140548-52141145	SK-N-SH	brain:	n/a	n/a
29	CTCF	chr19:52140759-52140929	Lung_OC	lung:	n/a	n/a
30	CTCF	chr19:52149993-52150038	GM19239	blood:	n/a	n/a
31	CTCF	chr19:52140720-52140870	HFF-Myc	foreskin:	n/a	n/a
32	CTCF	chr19:52140741-52140925	GM10266	blood:	n/a	n/a
33	CTCF	chr19:52140653-52140991	GM12878	blood:	n/a	n/a
34	CTCF	chr19:52140740-52140890	AG10803	skin:	n/a	n/a
35	CTCF	chr19:52149824-52149845	GM19239	blood:	n/a	n/a
36	CTCF	chr19:52140800-52140950	BJ	skin:	n/a	n/a
37	CTCF	chr19:52140740-52140890	GM06990	blood:	n/a	n/a
38	CTCF	chr19:52140740-52140890	SAEC	small airway:	n/a	n/a
39	CTCF	chr19:52140740-52140890	NHLF	lung:	n/a	n/a
40	CTCF	chr19:52140780-52140930	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr19:52140720-52140870	NHEK	skin:	n/a	n/a
42	CTCF	chr19:52140797-52140906	MCF-7	breast:	n/a	n/a
43	CTCF	chr19:52141112-52141120	Gliobla	brain:	n/a	n/a
44	CTCF	chr19:52141020-52141170	K562	blood:	n/a	n/a
45	CTCF	chr19:52140680-52140908	HepG2	liver:	n/a	n/a
46	CTCF	chr19:52141040-52141190	GM12866	blood:	n/a	n/a
47	CTCF	chr19:52141072-52141194	K562	blood:	n/a	n/a
48	CTCF	chr19:52140740-52140890	GM12869	blood:	n/a	n/a
49	CTCF	chr19:52140760-52140910	GM06990	blood:	n/a	n/a
50	CTCF	chr19:52140860-52140869	GM19239	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:52150634-52150684	HPAEpiC	pulmonary alveolar:	n/a
2	chr19:52150634-52150684	T-47D	breast:	n/a
3	chr19:52150233-52150283	ovcar-3	ovarian:	n/a
4	chr19:52150230-52150280	H1-hESC	embryonic stem cell:	embryo
5	chr19:52146598-52146648	HCPEpiC	choroid plexus:	n/a
6	chr19:52146598-52146648	ECC-1	luminal epithelium:	n/a
7	chr19:52150634-52150684	HUVEC	blood vessel:	n/a
8	chr19:52150233-52150283	K562	blood:	n/a
9	chr19:52150634-52150684	PANC-1	pancreas:	n/a
10	chr19:52140097-52140147	SK-N-SH	brain:	n/a
11	chr19:52150233-52150283	HMEC	breast:	n/a
12	chr19:52150634-52150684	GM12892	blood:	n/a
13	chr19:52146598-52146648	SK-N-SH_RA	brain:	n/a
14	chr19:52148354-52148404	HIPEpiC	eye:	n/a
15	chr19:52140097-52140147	ovcar-3	ovarian:	n/a
16	chr19:52148354-52148404	MCF10A-Er-Src	breast:	n/a
17	chr19:52150634-52150684	HEEpiC	esophagus:	n/a
18	chr19:52148354-52148404	ECC-1	luminal epithelium:	n/a
19	chr19:52150547-52150597	HCPEpiC	choroid plexus:	n/a
20	chr19:52150233-52150283	GM12878	blood:	n/a
21	chr19:52140097-52140147	MCF-7	breast:	n/a
22	chr19:52150233-52150283	HPAEpiC	pulmonary alveolar:	n/a
23	chr19:52140097-52140147	MCF10A-Er-Src	breast:	n/a
24	chr19:52150634-52150684	NH-A	brain:	n/a
25	chr19:52150230-52150280	PrEC	prostate:	n/a
26	chr19:52150547-52150597	GM12891	blood:	n/a
27	chr19:52150230-52150280	K562	blood:	n/a
28	chr19:52140097-52140147	GM06990	blood:	n/a
29	chr19:52148354-52148404	ProgFib	skin:	n/a
30	chr19:52150233-52150283	SK-N-SH_RA	brain:	n/a
31	chr19:52150233-52150283	Caco-2	colon:	n/a
32	chr19:52140097-52140147	AG09319	gingival:	n/a
33	chr19:52140097-52140147	SK-N-MC	brain:	n/a
34	chr19:52140097-52140147	K562	blood:	n/a
35	chr19:52140097-52140147	Jurkat	blood:	n/a
36	chr19:52140097-52140147	A549	lung:	n/a
37	chr19:52146598-52146648	SKMC	muscle:	n/a
38	chr19:52150233-52150283	LNCaP	prostate:	n/a
39	chr19:52148354-52148404	Jurkat	blood:	n/a
40	chr19:52148354-52148404	HNPCEpiC	eye:	n/a
41	chr19:52150230-52150280	AG09319	gingival:	n/a
42	chr19:52150634-52150684	SAEC	small airway:	n/a
43	chr19:52140097-52140147	GM12892	blood:	n/a
44	chr19:52148354-52148404	Hela-S3	cervix:	n/a
45	chr19:52146598-52146648	RPTEC	kidney:	n/a
46	chr19:52146598-52146648	A549	lung:	n/a
47	chr19:52146598-52146648	AG04449	skin:	fetal
48	chr19:52150634-52150684	PrEC	prostate:	n/a
49	chr19:52150634-52150684	AG09319	gingival:	n/a
50	chr19:52150634-52150684	ECC-1	luminal epithelium:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:52143293..52145764-chr19:52146395..52148250,2	K562	blood:
2	chr19:52110923..52111673-chr19:52140530..52141292,3	MCF-7	breast:
3	chr19:51924865..51925857-chr19:52140333..52141234,3	K562	blood:
4	chr19:52143293..52145764-chr19:52146395..52148250,2	K562	blood:
5	chr19:51960903..51963783-chr19:52139621..52141126,2	K562	blood:
6	chr19:52017645..52019212-chr19:52145235..52147486,2	MCF-7	breast:
7	chr19:51978649..51980839-chr19:52139351..52142005,2	K562	blood:
8	chr19:51975813..51976889-chr19:52140105..52142089,6	K562	blood:
9	chr19:52050848..52053096-chr19:52143769..52145532,2	K562	blood:
10	chr19:52110942..52111788-chr19:52140328..52140831,2	K562	blood:
11	chr19:52140352..52141294-chr19:52160036..52160673,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SIGLEC14-1	chr19:52148730-52148798	ENSG00000258669.1

No data

Variant related genes	Relation type
SIGLEC14	TF binding region
ENSG00000268500	TF binding region
RPL7P51	TF binding region
SIGLEC5	TF binding region
SIGLEC14	CpG island
ENSG00000268500	CpG island
RPL7P51	CpG island
SIGLEC5	CpG island
ENSG00000213822	chromatin interactions
ENSG00000105366	chromatin interactions

Extended variants
information (count: 445 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:445 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550263411	chr19:52137668-52137669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs80042996	chr19:52137726-52137727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs145354409	chr19:52137771-52137772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs112104828	chr19:52137776-52137777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs553895014	chr19:52137815-52137816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs190267663	chr19:52137843-52137844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs533783601	chr19:52137877-52137878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs558421209	chr19:52137888-52137889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs376015481	chr19:52137890-52137891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs142399986	chr19:52137956-52137957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs558307327	chr19:52137958-52137959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs34813977	chr19:52137978-52137979	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs117265651	chr19:52138009-52138010	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs143862558	chr19:52138034-52138035	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs148282382	chr19:52138148-52138149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs10418659	chr19:52138199-52138200	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs374907426	chr19:52138265-52138266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs555310921	chr19:52138275-52138276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs111643547	chr19:52138367-52138368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs369118965	chr19:52138416-52138417	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs72094623	chr19:52138456-52138457	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs573873047	chr19:52138485-52138486	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs150791339	chr19:52138499-52138500	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs576468784	chr19:52138509-52138510	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs10419270	chr19:52138517-52138518	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs10421037	chr19:52138562-52138563	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs10419309	chr19:52138563-52138564	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs117763162	chr19:52138569-52138570	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs563382171	chr19:52138585-52138586	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs547879145	chr19:52138696-52138697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs10419738	chr19:52138703-52138704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs566272362	chr19:52138719-52138720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs530561610	chr19:52138745-52138746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs527395394	chr19:52138784-52138785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs181930827	chr19:52138826-52138827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs185008616	chr19:52138839-52138840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs537714625	chr19:52138848-52138849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs139149410	chr19:52138869-52138870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs569132560	chr19:52138889-52138890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs373882960	chr19:52138929-52138930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs536688508	chr19:52138968-52138969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs143586116	chr19:52138993-52138994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs190202178	chr19:52139026-52139027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs540754821	chr19:52139049-52139050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs74924499	chr19:52139055-52139056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs562146818	chr19:52139064-52139065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs577104601	chr19:52139114-52139115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs574546970	chr19:52139115-52139116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs199522727	chr19:52139148-52139149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs111392470	chr19:52139150-52139151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Adrenocortical carcinoma	18281524	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Cancer	20164920	CNVD
Melanoma	17363583	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:148 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:52134200-52140200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr19:52134200-52144400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr19:52134400-52138000	Weak transcription	Primary B cells from cord blood	blood
4	chr19:52134600-52137800	Weak transcription	Primary B cells from peripheral blood	blood
5	chr19:52134600-52139400	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr19:52134600-52139400	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr19:52135200-52140000	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr19:52137800-52141200	Enhancers	Primary B cells from peripheral blood	blood
9	chr19:52138000-52140600	Enhancers	Primary B cells from cord blood	blood
10	chr19:52139400-52141200	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr19:52139400-52141400	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr19:52139600-52140800	Active TSS	Primary neutrophils fromperipheralblood	blood
13	chr19:52140000-52140200	Enhancers	Placenta Amnion	Placenta Amnion
14	chr19:52140200-52140600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
15	chr19:52141200-52142400	Weak transcription	Primary B cells from peripheral blood	blood
16	chr19:52141200-52142600	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr19:52141400-52142200	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr19:52142200-52143600	Strong transcription	Primary monocytes fromperipheralblood	blood
19	chr19:52142400-52143600	Strong transcription	Primary B cells from peripheral blood	blood
20	chr19:52142600-52144000	Strong transcription	Monocytes-CD14+_RO01746	blood
21	chr19:52143600-52147800	Genic enhancers	Primary monocytes fromperipheralblood	blood
22	chr19:52143600-52147800	Genic enhancers	Primary B cells from peripheral blood	blood
23	chr19:52144000-52144200	Weak transcription	Monocytes-CD14+_RO01746	blood
24	chr19:52144200-52145400	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr19:52144400-52144600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
26	chr19:52144600-52146400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr19:52144600-52146800	Weak transcription	Spleen	Spleen
28	chr19:52145400-52145600	Genic enhancers	Monocytes-CD14+_RO01746	blood
29	chr19:52145400-52148000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr19:52145600-52147800	Enhancers	Primary B cells from cord blood	blood
31	chr19:52145600-52147800	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood
32	chr19:52146400-52147200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr19:52146400-52147800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr19:52146400-52148400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
35	chr19:52146800-52147200	Weak transcription	Lung	lung
36	chr19:52146800-52147800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr19:52146800-52148000	Genic enhancers	Spleen	Spleen
38	chr19:52146800-52150200	Active TSS	Primary neutrophils fromperipheralblood	blood
39	chr19:52147200-52147400	Enhancers	Lung	lung
40	chr19:52147200-52148200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr19:52147200-52153400	Weak transcription	Right Atrium	heart
42	chr19:52147400-52147600	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
43	chr19:52147400-52149200	Enhancers	GM12878-XiMat	blood
44	chr19:52147600-52147800	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
45	chr19:52147600-52147800	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr19:52147600-52148000	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr19:52147800-52148000	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
48	chr19:52147800-52148000	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 29	rectum
49	chr19:52147800-52148200	Transcr. at gene 5' and 3'	Primary monocytes fromperipheralblood	blood
50	chr19:52147800-52148200	Bivalent/Poised TSS	Brain Anterior Caudate	brain

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