Variant report

Variant	nsv912297
Chromosome Location	chr19:52213743-52227066
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:378)
CpG islands
(count:856)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:378 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:52216127-52216237	K562	blood:	n/a	n/a
2	BACH1	chr19:52222347-52223096	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr19:52216051-52216193	K562	blood:	n/a	n/a
4	BCL3	chr19:52214225-52215393	A549	lung:	n/a	n/a
5	BCL3	chr19:52216373-52217627	A549	lung:	n/a	n/a
6	BCL3	chr19:52226655-52227156	GM12878	blood:	n/a	n/a
7	BCL3	chr19:52213388-52214137	A549	lung:	n/a	n/a
8	BCL3	chr19:52215627-52217718	A549	lung:	n/a	n/a
9	BCL3	chr19:52217768-52219081	A549	lung:	n/a	n/a
10	BCL3	chr19:52226672-52227115	GM12878	blood:	n/a	n/a
11	BCL3	chr19:52218019-52218627	A549	lung:	n/a	n/a
12	BCL3	chr19:52212749-52214169	A549	lung:	n/a	n/a
13	BCL3	chr19:52226278-52226570	GM12878	blood:	n/a	n/a
14	CBX3	chr19:52218122-52218491	K562	blood:	n/a	n/a
15	CCNT2	chr19:52216660-52217240	K562	blood:	n/a	n/a
16	CEBPB	chr19:52216011-52216359	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr19:52215959-52216357	MCF-7	breast:	n/a	n/a
18	CEBPB	chr19:52215928-52216375	MCF-7	breast:	n/a	n/a
19	CEBPB	chr19:52215995-52216293	K562	blood:	n/a	n/a
20	CEBPB	chr19:52223189-52223224	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr19:52215981-52216307	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr19:52224388-52224592	K562	blood:	n/a	n/a
23	CTCF	chr19:52216060-52216210	BE2_C	brain:	n/a	n/a
24	CTCF	chr19:52216060-52216210	HAc	cerebellar:	n/a	n/a
25	CTCF	chr19:52215928-52216313	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr19:52215862-52216287	K562	blood:	n/a	n/a
27	CTCF	chr19:52216060-52216210	Caco-2	colon:	n/a	n/a
28	CTCF	chr19:52216005-52216229	GM13977	blood:	n/a	n/a
29	CTCF	chr19:52222520-52222553	Fibrobl	skin:	n/a	n/a
30	CTCF	chr19:52216080-52216230	GM06990	blood:	n/a	n/a
31	CTCF	chr19:52216020-52216170	HCT-116	colon:	n/a	n/a
32	CTCF	chr19:52215971-52216272	LNCaP	prostate:	n/a	n/a
33	CTCF	chr19:52215947-52216233	K562	blood:	n/a	n/a
34	CTCF	chr19:52216000-52216150	MCF-7	breast:	n/a	n/a
35	CTCF	chr19:52222502-52222652	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr19:52215985-52216252	K562	blood:	n/a	n/a
37	CTCF	chr19:52215992-52216262	MCF-7	breast:	n/a	n/a
38	CTCF	chr19:52215980-52216130	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr19:52216080-52216230	GM12867	blood:	n/a	n/a
40	CTCF	chr19:52216020-52216170	GM12872	blood:	n/a	n/a
41	CTCF	chr19:52216071-52216164	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr19:52216057-52216182	GM10248	blood:	n/a	n/a
43	CTCF	chr19:52215603-52216757	A549	lung:	n/a	n/a
44	CTCF	chr19:52216020-52216170	AG09309	skin:	n/a	n/a
45	CTCF	chr19:52216040-52216190	GM12872	blood:	n/a	n/a
46	CTCF	chr19:52216040-52216190	MCF-7	breast:	n/a	n/a
47	CTCF	chr19:52216060-52216210	GM12875	blood:	n/a	n/a
48	CTCF	chr19:52215952-52216300	K562	blood:	n/a	n/a
49	CTCF	chr19:52216060-52216210	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr19:52216080-52216230	GM12866	blood:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:52216558-52216608	HAEpiC	amniotic membrane:	n/a
2	chr19:52222446-52222496	Hela-S3	cervix:	n/a
3	chr19:52216558-52216608	HAEpiC	amniotic membrane:	n/a
4	chr19:52222446-52222496	Hela-S3	cervix:	n/a
5	chr19:52225777-52225827	AG04450	lung:	fetal
6	chr19:52222446-52222496	RPTEC	kidney:	n/a
7	chr19:52222446-52222496	HRPEpiC	eye:	n/a
8	chr19:52218453-52218503	SAEC	small airway:	n/a
9	chr19:52213977-52214027	ECC-1	luminal epithelium:	n/a
10	chr19:52222446-52222496	K562	blood:	n/a
11	chr19:52216558-52216608	CMK	blood:	n/a
12	chr19:52219484-52219534	SKMC	muscle:	n/a
13	chr19:52222198-52222248	AG04449	skin:	fetal
14	chr19:52223620-52223670	HRE	kidney:	n/a
15	chr19:52225777-52225827	SAEC	small airway:	n/a
16	chr19:52222698-52222748	RPTEC	kidney:	n/a
17	chr19:52213977-52214027	HL-60	blood:	n/a
18	chr19:52219484-52219534	U87	brain:	n/a
19	chr19:52216726-52216776	GM12892	blood:	n/a
20	chr19:52223099-52223149	SK-N-MC	brain:	n/a
21	chr19:52222698-52222748	MCF-7	breast:	n/a
22	chr19:52222698-52222748	HepG2	liver:	n/a
23	chr19:52216558-52216608	AoSMC	blood vessel:	n/a
24	chr19:52216726-52216776	U87	brain:	n/a
25	chr19:52217022-52217072	HL-60	blood:	n/a
26	chr19:52217388-52217438	HMEC	breast:	n/a
27	chr19:52222198-52222248	CMK	blood:	n/a
28	chr19:52216726-52216776	GM12878	blood:	n/a
29	chr19:52216726-52216776	PrEC	prostate:	n/a
30	chr19:52222698-52222748	A549	lung:	n/a
31	chr19:52223620-52223670	NH-A	brain:	n/a
32	chr19:52216726-52216776	T-47D	breast:	n/a
33	chr19:52217022-52217072	GM19239	blood:	n/a
34	chr19:52222198-52222248	RPTEC	kidney:	n/a
35	chr19:52213977-52214027	SK-N-SH	brain:	n/a
36	chr19:52217022-52217072	GM06990	blood:	n/a
37	chr19:52222198-52222248	K562	blood:	n/a
38	chr19:52218453-52218503	NHDF-neo	bronchial:	n/a
39	chr19:52213977-52214027	NH-A	brain:	n/a
40	chr19:52222198-52222248	NHDF-neo	bronchial:	n/a
41	chr19:52218453-52218503	GM19239	blood:	n/a
42	chr19:52222198-52222248	HCT-116	colon:	n/a
43	chr19:52225777-52225827	GM19239	blood:	n/a
44	chr19:52222431-52222481	ECC-1	luminal epithelium:	n/a
45	chr19:52217022-52217072	NT2-D1	testis:	n/a
46	chr19:52216726-52216776	LNCaP	prostate:	n/a
47	chr19:52222198-52222248	MCF10A-Er-Src	breast:	n/a
48	chr19:52222431-52222481	AG09309	skin:	n/a
49	chr19:52213977-52214027	GM12892	blood:	n/a
50	chr19:52222698-52222748	HMEC	breast:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:52213474..52215839-chr19:52229447..52232151,2	K562	blood:
2	chr19:52216085..52216905-chr19:52311568..52312097,3	MCF-7	breast:
3	chr19:52213474..52218033-chr19:52227253..52233222,6	K562	blood:
4	chr19:52197003..52199691-chr19:52213714..52215992,2	MCF-7	breast:
5	chr19:52215836..52216573-chr19:52280774..52281726,5	MCF-7	breast:
6	chr19:52210301..52211912-chr19:52215119..52217997,2	K562	blood:
7	chr19:52211595..52213921-chr19:52286963..52288731,2	MCF-7	breast:
8	chr19:52216500..52217173-chr19:52286806..52287310,2	MCF-7	breast:
9	chr19:52205873..52210007-chr19:52211189..52216257,9	K562	blood:
10	chr19:52216356..52218873-chr19:52218955..52221873,2	MCF-7	breast:
11	chr19:52216020..52218332-chr19:52241843..52243372,2	MCF-7	breast:
12	chr19:52213601..52216157-chr19:52216893..52219769,2	MCF-7	breast:
13	chr19:52219107..52222029-chr19:52222398..52224089,2	K562	blood:
14	chr19:52218179..52219711-chr19:52309357..52312195,2	MCF-7	breast:
15	chr19:52213601..52216157-chr19:52216893..52219769,2	MCF-7	breast:
16	chr19:52215661..52216484-chr19:52286408..52287282,3	MCF-7	breast:
17	chr19:52216356..52218873-chr19:52218955..52221873,2	MCF-7	breast:
18	chr19:52213445..52215561-chr19:52311102..52312961,2	MCF-7	breast:
19	chr19:52214081..52217958-chr19:52222891..52225862,3	K562	blood:

No data

Variant related genes	Relation type
HAS1	TF binding region
HAS1	CpG island
ENSG00000105509	chromatin interactions
ENSG00000182310	chromatin interactions

Extended variants
information (count: 569 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:569 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2864922	chr19:52213743-52213744	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs74394747	chr19:52213860-52213861	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs566341389	chr19:52213888-52213889	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs113373586	chr19:52213904-52213905	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs189164721	chr19:52213969-52213970	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs549321909	chr19:52213977-52213978	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs568443951	chr19:52213994-52213995	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs146067336	chr19:52214005-52214006	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs116086627	chr19:52214068-52214069	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs34660516	chr19:52214079-52214080	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs566211644	chr19:52214098-52214099	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs539558765	chr19:52214122-52214123	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs558296601	chr19:52214139-52214140	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs576582509	chr19:52214200-52214201	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs112268401	chr19:52214299-52214300	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs543685192	chr19:52214311-52214312	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs4802845	chr19:52214328-52214329	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs578167471	chr19:52214359-52214360	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs573290879	chr19:52214366-52214367	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs540670016	chr19:52214399-52214400	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs73054899	chr19:52214445-52214446	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs533007578	chr19:52214449-52214450	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs544795309	chr19:52214460-52214461	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs563471952	chr19:52214496-52214497	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs115351021	chr19:52214497-52214498	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs558421948	chr19:52214565-52214566	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs4801888	chr19:52214567-52214568	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs111407070	chr19:52214634-52214635	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs138837885	chr19:52214636-52214637	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs547772019	chr19:52214679-52214680	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs543756111	chr19:52214699-52214700	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs142800880	chr19:52214705-52214706	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs375300986	chr19:52214711-52214712	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs562885454	chr19:52214742-52214743	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs535320630	chr19:52214750-52214751	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs77082711	chr19:52214751-52214752	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs551611970	chr19:52214778-52214779	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs75158894	chr19:52214781-52214782	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs372374053	chr19:52214865-52214866	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs555635438	chr19:52214905-52214906	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs147495866	chr19:52214921-52214922	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs534998329	chr19:52214946-52214947	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs573768968	chr19:52214977-52214978	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs79215972	chr19:52214979-52214980	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs577591785	chr19:52214982-52214983	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs35898078	chr19:52215031-52215032	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs34803450	chr19:52215032-52215033	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs141858942	chr19:52215048-52215049	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs563274094	chr19:52215056-52215057	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs150619894	chr19:52215066-52215067	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Ovarian cancer	22355333	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:293 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:52208000-52216600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr19:52208400-52216200	Weak transcription	Fetal Brain Male	brain
3	chr19:52208400-52218200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr19:52208400-52220200	Weak transcription	Ovary	ovary
5	chr19:52208600-52214400	Weak transcription	Primary B cells from cord blood	blood
6	chr19:52208600-52214400	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr19:52208600-52218800	Weak transcription	Fetal Heart	heart
8	chr19:52208800-52214600	Weak transcription	GM12878-XiMat	blood
9	chr19:52208800-52222000	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr19:52209000-52214800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr19:52209600-52213800	Weak transcription	Brain Cingulate Gyrus	brain
12	chr19:52209600-52222400	Weak transcription	Spleen	Spleen
13	chr19:52210000-52214800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr19:52210400-52216400	Weak transcription	Brain Anterior Caudate	brain
15	chr19:52210400-52216800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr19:52210400-52218200	Weak transcription	Primary T helper cells fromperipheralblood	blood
17	chr19:52210400-52222000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr19:52210800-52213800	Weak transcription	Brain Substantia Nigra	brain
19	chr19:52210800-52215800	Weak transcription	Fetal Kidney	kidney
20	chr19:52210800-52216400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr19:52211000-52214400	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr19:52211000-52215000	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr19:52211000-52216200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr19:52211000-52216200	Weak transcription	HMEC	breast
25	chr19:52211000-52218000	Weak transcription	Brain Hippocampus Middle	brain
26	chr19:52211200-52213800	Weak transcription	Fetal Thymus	thymus
27	chr19:52211200-52216400	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr19:52211200-52216600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr19:52211200-52218200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr19:52211400-52213800	Weak transcription	HSMMtube	muscle
31	chr19:52211400-52214000	Weak transcription	Fetal Intestine Small	intestine
32	chr19:52211400-52215000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr19:52211400-52215200	Weak transcription	Fetal Muscle Leg	muscle
34	chr19:52211400-52216600	Weak transcription	Fetal Lung	lung
35	chr19:52211400-52219200	Weak transcription	Brain Angular Gyrus	brain
36	chr19:52211600-52214200	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr19:52211600-52214600	Weak transcription	Adipose Nuclei	Adipose
38	chr19:52211600-52214600	Weak transcription	NH-A	brain
39	chr19:52211600-52216200	Weak transcription	Osteobl	bone
40	chr19:52211600-52218400	Weak transcription	K562	blood
41	chr19:52211800-52215600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr19:52211800-52216200	Weak transcription	NHLF	lung
43	chr19:52213000-52217000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr19:52213200-52214200	Enhancers	HSMM	muscle
45	chr19:52213200-52214600	Weak transcription	A549	lung
46	chr19:52213200-52216600	Enhancers	Primary B cells from peripheral blood	blood
47	chr19:52213200-52217000	Weak transcription	Esophagus	oesophagus
48	chr19:52213200-52217200	Weak transcription	Placenta	Placenta
49	chr19:52213400-52213800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr19:52213400-52214000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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