Variant report

Variant	nsv1065345
Chromosome Location	chr19:53199614-53254617
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1253)
CpG islands
(count:1405)
Chromatin interactive
region (count:18)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1253 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:53238204-53238593	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:53228598-53228749	K562	blood:	n/a	n/a
3	ARID3A	chr19:53227189-53227366	K562	blood:	n/a	n/a
4	ARID3A	chr19:53228340-53228382	K562	blood:	n/a	n/a
5	ARID3A	chr19:53227580-53227746	HepG2	liver:	n/a	n/a
6	ATF1	chr19:53233027-53233245	K562	blood:	n/a	n/a
7	ATF1	chr19:53227069-53227523	K562	blood:	n/a	n/a
8	ATF1	chr19:53238100-53238672	K562	blood:	n/a	n/a
9	ATF1	chr19:53219224-53219418	K562	blood:	n/a	n/a
10	ATF2	chr19:53239019-53239370	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr19:53238937-53239428	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr19:53228814-53229132	K562	blood:	n/a	n/a
13	ATF3	chr19:53238046-53238465	K562	blood:	n/a	n/a
14	BACH1	chr19:53238107-53238408	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr19:53245884-53246161	GM12878	blood:	n/a	chr19:53245986-53245996 chr19:53245985-53245996 chr19:53245990-53246000
16	BATF	chr19:53218901-53219394	GM12878	blood:	n/a	chr19:53219199-53219209 chr19:53219203-53219213
17	BATF	chr19:53245915-53246089	GM12878	blood:	n/a	chr19:53245986-53245996 chr19:53245985-53245996 chr19:53245990-53246000
18	BATF	chr19:53218901-53219396	GM12878	blood:	n/a	chr19:53219199-53219209 chr19:53219203-53219213
19	BATF	chr19:53243525-53243726	GM12878	blood:	n/a	n/a
20	BCL11A	chr19:53219022-53219347	GM12878	blood:	n/a	chr19:53219201-53219210
21	BCL11A	chr19:53238080-53238304	GM12878	blood:	n/a	n/a
22	BCL11A	chr19:53240555-53240723	GM12878	blood:	n/a	n/a
23	BCL11A	chr19:53219085-53219334	GM12878	blood:	n/a	chr19:53219201-53219210
24	BCL3	chr19:53235753-53236010	GM12878	blood:	n/a	n/a
25	BCLAF1	chr19:53237957-53238447	GM12878	blood:	n/a	chr19:53238422-53238435
26	BHLHE40	chr19:53238124-53238500	K562	blood:	n/a	n/a
27	BHLHE40	chr19:53238239-53238453	GM12878	blood:	n/a	n/a
28	BHLHE40	chr19:53227179-53227448	K562	blood:	n/a	n/a
29	BHLHE40	chr19:53228364-53229160	K562	blood:	n/a	n/a
30	BHLHE40	chr19:53229503-53229523	K562	blood:	n/a	n/a
31	BRCA1	chr19:53219929-53220101	H1-hESC	embryonic stem cell:	n/a	n/a
32	BRCA1	chr19:53238025-53238612	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr19:53238114-53238309	GM12878	blood:	n/a	n/a
34	CBX3	chr19:53208757-53209318	K562	blood:	n/a	n/a
35	CBX3	chr19:53238062-53238800	K562	blood:	n/a	n/a
36	CBX3	chr19:53226892-53227577	K562	blood:	n/a	n/a
37	CBX3	chr19:53238334-53238591	K562	blood:	n/a	n/a
38	CBX3	chr19:53228183-53229250	K562	blood:	n/a	n/a
39	CCNT2	chr19:53228944-53229189	K562	blood:	n/a	n/a
40	CCNT2	chr19:53228300-53228706	K562	blood:	n/a	n/a
41	CCNT2	chr19:53237915-53238524	K562	blood:	n/a	chr19:53238372-53238381
42	CEBPB	chr19:53232598-53232808	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr19:53238741-53238842	K562	blood:	n/a	chr19:53238809-53238820
44	CEBPB	chr19:53219942-53220105	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr19:53234585-53234747	HepG2	liver:	n/a	chr19:53234679-53234690
46	CEBPB	chr19:53237971-53238451	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr19:53227084-53227394	K562	blood:	n/a	n/a
48	CEBPB	chr19:53212256-53212412	K562	blood:	n/a	chr19:53212306-53212319 chr19:53212308-53212319 chr19:53212308-53212317 chr19:53212308-53212317 chr19:53212308-53212317 chr19:53212308-53212317
49	CEBPB	chr19:53232623-53232823	IMR90	lung:	n/a	n/a
50	CEBPB	chr19:53251834-53252159	HepG2	liver:	n/a	chr19:53251983-53251994

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53207899-53207949	SK-N-SH_RA	brain:	n/a
2	chr19:53207899-53207949	CMK	blood:	n/a
3	chr19:53207899-53207949	SK-N-SH_RA	brain:	n/a
4	chr19:53207899-53207949	CMK	blood:	n/a
5	chr19:53238413-53238463	HIPEpiC	eye:	n/a
6	chr19:53237645-53237695	HL-60	blood:	n/a
7	chr19:53237871-53237921	GM19239	blood:	n/a
8	chr19:53238492-53238542	NHBE	bronchial:	n/a
9	chr19:53225441-53225491	Jurkat	blood:	n/a
10	chr19:53238254-53238304	HRPEpiC	eye:	n/a
11	chr19:53238434-53238484	HNPCEpiC	eye:	n/a
12	chr19:53237862-53237912	SK-N-SH_RA	brain:	n/a
13	chr19:53238254-53238304	HMEC	breast:	n/a
14	chr19:53239200-53239250	PANC-1	pancreas:	n/a
15	chr19:53238498-53238548	HRCEpiC	kidney:	n/a
16	chr19:53238445-53238495	PFSK-1	brain:	n/a
17	chr19:53239146-53239196	HL-60	blood:	n/a
18	chr19:53234126-53234176	HMEC	breast:	n/a
19	chr19:53242420-53242470	AG04450	lung:	fetal
20	chr19:53238434-53238484	GM06990	blood:	n/a
21	chr19:53234126-53234176	CMK	blood:	n/a
22	chr19:53238434-53238484	HCPEpiC	choroid plexus:	n/a
23	chr19:53238498-53238548	GM12878	blood:	n/a
24	chr19:53237862-53237912	U87	brain:	n/a
25	chr19:53237645-53237695	AG09309	skin:	n/a
26	chr19:53242420-53242470	HRPEpiC	eye:	n/a
27	chr19:53229096-53229146	GM06990	blood:	n/a
28	chr19:53239200-53239250	HIPEpiC	eye:	n/a
29	chr19:53229766-53229816	AG09319	gingival:	n/a
30	chr19:53239200-53239250	GM12892	blood:	n/a
31	chr19:53242420-53242470	Caco-2	colon:	n/a
32	chr19:53229096-53229146	PrEC	prostate:	n/a
33	chr19:53242420-53242470	SK-N-MC	brain:	n/a
34	chr19:53238434-53238484	HRPEpiC	eye:	n/a
35	chr19:53233083-53233133	Caco-2	colon:	n/a
36	chr19:53234126-53234176	SAEC	small airway:	n/a
37	chr19:53233245-53233295	CMK	blood:	n/a
38	chr19:53238413-53238463	T-47D	breast:	n/a
39	chr19:53239146-53239196	AG04450	lung:	fetal
40	chr19:53239200-53239250	HMEC	breast:	n/a
41	chr19:53239200-53239250	AG04449	skin:	fetal
42	chr19:53237871-53237921	AG09309	skin:	n/a
43	chr19:53239200-53239250	AG04450	lung:	fetal
44	chr19:53239200-53239250	K562	blood:	n/a
45	chr19:53239146-53239196	HRE	kidney:	n/a
46	chr19:53233164-53233214	K562	blood:	n/a
47	chr19:53228974-53229024	ovcar-3	ovarian:	n/a
48	chr19:53237862-53237912	HL-60	blood:	n/a
49	chr19:53238445-53238495	ovcar-3	ovarian:	n/a
50	chr19:53229766-53229816	AoSMC	blood vessel:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:53227642..53230112-chr19:53236849..53239461,2	K562	blood:
2	chr19:53115970..53118193-chr19:53236786..53238588,2	K562	blood:
3	chr19:53226674..53228672-chr19:53232730..53234940,2	K562	blood:
4	chr19:53226674..53228672-chr19:53232730..53234940,2	K562	blood:
5	chr19:53237008..53239147-chr19:53540786..53542527,2	MCF-7	breast:
6	chr19:53227642..53230112-chr19:53236849..53239461,2	K562	blood:
7	chr19:53227707..53230460-chr19:53236213..53239636,6	K562	blood:
8	chr19:53236244..53237950-chr19:53242142..53244901,2	K562	blood:
9	chr19:53236244..53237950-chr19:53242142..53244901,2	K562	blood:
10	chr19:53215678..53217452-chr19:53219568..53222029,2	K562	blood:
11	chr19:53199473..53201886-chr19:53208932..53211700,2	K562	blood:
12	chr19:53199473..53201886-chr19:53208932..53211700,2	K562	blood:
13	chr19:53233250..53234773-chr19:53236233..53238057,2	K562	blood:
14	chr19:53233250..53234773-chr19:53236233..53238057,2	K562	blood:
15	chr19:53236450..53239197-chr19:53240698..53243642,2	K562	blood:
16	chr19:53227707..53230460-chr19:53236213..53239636,6	K562	blood:
17	chr14:93214475..93215046-chr19:53237894..53238692,2	Hela-S3	cervix:
18	chr19:53215678..53217452-chr19:53219568..53222029,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF83-5	chr19:53233159-53233258	NONHSAT067579
2	lnc-ZNF83-5	chr19:53231983-53232084	NONHSAT067580
3	lnc-ZNF83-5	chr19:53226674-53227917	NONHSAT067581
4	lnc-ZNF83-5	chr19:53231983-53232084	NONHSAT067579
5	lnc-ZNF83-3	chr19:53211457-53211582	NONHSAT067577
6	lnc-ZNF83-5	chr19:53224436-53224520	NONHSAT067580
7	lnc-ZNF83-3	chr19:53211674-53212084	NONHSAT067577
8	lnc-ZNF83-5	chr19:53238254-53238326	NONHSAT067579
9	lnc-ZNF83-5	chr19:53224406-53224520	NONHSAT067579
10	lnc-ZNF83-5	chr19:53238254-53238268	NONHSAT067580
11	lnc-ZNF83-5	chr19:53227124-53227242	NONHSAT067579
12	lnc-ZNF83-5	chr19:53233159-53233258	NONHSAT067580

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ZNF611	hsa-miR-155-5p	chr19:53207486-53207509

Variant related genes	Relation type
ZNF611	TF binding region
ZNF611	CpG island
ENSG00000213020	chromatin interactions
ENSG00000242779	chromatin interactions
ENSG00000167766	chromatin interactions
ENSG00000100600	chromatin interactions

Extended variants
information (count: 3098 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:3098 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181889532	chr19:53199685-53199686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs114376400	chr19:53199715-53199716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs201263235	chr19:53199718-53199719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs575945876	chr19:53199744-53199745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs149830795	chr19:53199746-53199747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs555143188	chr19:53199766-53199767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573774225	chr19:53199799-53199800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs113047891	chr19:53199816-53199817	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs78393293	chr19:53199899-53199900	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs187011499	chr19:53199910-53199911	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs148587783	chr19:53199916-53199917	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs144549226	chr19:53199942-53199943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs192046069	chr19:53199977-53199978	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs550450560	chr19:53199978-53199979	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs114816305	chr19:53199990-53199991	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs202074881	chr19:53200009-53200010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs556585978	chr19:53200010-53200011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs111351707	chr19:53200011-53200012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs199671744	chr19:53200012-53200013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs375651617	chr19:53200015-53200016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs368307202	chr19:53200016-53200017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs371914640	chr19:53200017-53200018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs201060331	chr19:53200028-53200029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs181711566	chr19:53200075-53200076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs547203423	chr19:53200077-53200078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs137906520	chr19:53200078-53200079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs76471771	chr19:53200081-53200082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs115261736	chr19:53200097-53200098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs539111126	chr19:53200113-53200114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs186666554	chr19:53200191-53200192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs530232182	chr19:53200194-53200195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs190176605	chr19:53200204-53200205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs548733654	chr19:53200252-53200253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs536992572	chr19:53200311-53200312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs4802986	chr19:53200324-53200325	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs146546461	chr19:53200420-53200421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs375701311	chr19:53200447-53200448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs534798509	chr19:53200448-53200449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs141247757	chr19:53200462-53200463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs112384356	chr19:53200526-53200527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs371736708	chr19:53200550-53200551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs375929933	chr19:53200557-53200558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs554131467	chr19:53200565-53200566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs374873206	chr19:53200579-53200580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs564476673	chr19:53200583-53200584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs576502558	chr19:53200586-53200587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs151279068	chr19:53200600-53200601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs369001657	chr19:53200613-53200614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs140815192	chr19:53200663-53200664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs529531758	chr19:53200680-53200681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
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
Breast cancer	21785460	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Adrenocortical carcinoma	18281524	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1920 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53194200-53207200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr19:53194600-53208400	Weak transcription	Hela-S3	cervix
3	chr19:53194600-53208800	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr19:53194800-53202600	Weak transcription	Stomach Mucosa	stomach
5	chr19:53194800-53205000	Weak transcription	Fetal Brain Female	brain
6	chr19:53194800-53207600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr19:53194800-53207600	Weak transcription	Brain Anterior Caudate	brain
8	chr19:53194800-53208400	Weak transcription	Stomach Smooth Muscle	stomach
9	chr19:53194800-53218800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr19:53195000-53207800	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr19:53195000-53210600	Weak transcription	Fetal Stomach	stomach
12	chr19:53195200-53207200	Weak transcription	Brain Germinal Matrix	brain
13	chr19:53195200-53207400	Weak transcription	Dnd41	blood
14	chr19:53195200-53207800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr19:53198000-53199800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr19:53198000-53201200	Enhancers	Placenta	Placenta
17	chr19:53198800-53202000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr19:53199400-53199800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr19:53199600-53200000	Enhancers	HepG2	liver
20	chr19:53199600-53207800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr19:53199600-53208800	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr19:53199800-53200000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr19:53199800-53207400	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr19:53200000-53202000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr19:53200000-53203200	Weak transcription	HepG2	liver
26	chr19:53201200-53202000	Weak transcription	Placenta	Placenta
27	chr19:53202000-53202400	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr19:53202000-53203400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr19:53202000-53204000	Enhancers	Placenta	Placenta
30	chr19:53202400-53204400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr19:53202800-53209000	Weak transcription	Fetal Heart	heart
32	chr19:53202800-53217400	ZNF genes & repeats	Liver	Liver
33	chr19:53203200-53207600	Enhancers	HepG2	liver
34	chr19:53203200-53208200	Weak transcription	Left Ventricle	heart
35	chr19:53203400-53205200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr19:53203400-53207400	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr19:53203400-53207800	Weak transcription	Fetal Lung	lung
38	chr19:53203600-53207800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr19:53203600-53207800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr19:53203800-53208000	Weak transcription	Fetal Muscle Leg	muscle
41	chr19:53204000-53204200	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr19:53204000-53204400	Weak transcription	Placenta	Placenta
43	chr19:53204200-53204600	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr19:53204200-53205400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr19:53204200-53208200	Weak transcription	Colon Smooth Muscle	Colon
46	chr19:53204400-53204600	Enhancers	Placenta	Placenta
47	chr19:53204400-53205400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr19:53204400-53206600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr19:53204400-53207600	Weak transcription	Adipose Nuclei	Adipose
50	chr19:53204400-53207800	Weak transcription	Brain Substantia Nigra	brain

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