Variant report

Variant	esv3397651
Chromosome Location	chr19:36326933-36377725
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1445)
CpG islands
(count:3665)
Chromatin interactive
region (count:71)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1445 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:36360868-36361320	K562	blood:	n/a	n/a
2	ARID3A	chr19:36346631-36346781	K562	blood:	n/a	n/a
3	ARID3A	chr19:36370646-36370941	K562	blood:	n/a	n/a
4	ARID3A	chr19:36373033-36373376	K562	blood:	n/a	n/a
5	ATF2	chr19:36376101-36376537	GM12878	blood:	n/a	n/a
6	ATF2	chr19:36376851-36377138	GM12878	blood:	n/a	n/a
7	ATF2	chr19:36342050-36342417	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr19:36360710-36361472	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr19:36370600-36370950	K562	blood:	n/a	chr19:36370838-36370847
10	ATF3	chr19:36335974-36336325	K562	blood:	n/a	n/a
11	BACH1	chr19:36346966-36347538	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr19:36370693-36370877	K562	blood:	n/a	n/a
13	BACH1	chr19:36336276-36336324	K562	blood:	n/a	n/a
14	BACH1	chr19:36337453-36337538	K562	blood:	n/a	n/a
15	BACH1	chr19:36359150-36359446	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr19:36351334-36352277	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr19:36336244-36336455	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr19:36334697-36335095	H1-hESC	embryonic stem cell:	n/a	n/a
19	BCL3	chr19:36359819-36361440	A549	lung:	n/a	chr19:36360912-36360921 chr19:36360553-36360562 chr19:36360410-36360418
20	BCL3	chr19:36337155-36337715	A549	lung:	n/a	chr19:36337209-36337216
21	BCL3	chr19:36370427-36371390	A549	lung:	n/a	chr19:36370882-36370891
22	BCL3	chr19:36336812-36337721	A549	lung:	n/a	chr19:36337209-36337216
23	BCLAF1	chr19:36376171-36376522	GM12878	blood:	n/a	n/a
24	BCLAF1	chr19:36376156-36376627	GM12878	blood:	n/a	n/a
25	BHLHE40	chr19:36349412-36349496	K562	blood:	n/a	n/a
26	BHLHE40	chr19:36336116-36337138	K562	blood:	n/a	n/a
27	BHLHE40	chr19:36370702-36371333	K562	blood:	n/a	chr19:36371166-36371175 chr19:36371159-36371180
28	BHLHE40	chr19:36352039-36352243	K562	blood:	n/a	n/a
29	BHLHE40	chr19:36339652-36339731	K562	blood:	n/a	n/a
30	BHLHE40	chr19:36346600-36346719	K562	blood:	n/a	n/a
31	BHLHE40	chr19:36353530-36353731	K562	blood:	n/a	n/a
32	BHLHE40	chr19:36370991-36371260	A549	lung:	n/a	chr19:36371166-36371175 chr19:36371159-36371180
33	BHLHE40	chr19:36370731-36371092	GM12878	blood:	n/a	n/a
34	BHLHE40	chr19:36370621-36371299	HepG2	liver:	n/a	chr19:36371166-36371175 chr19:36371159-36371180
35	BHLHE40	chr19:36336214-36337134	HepG2	liver:	n/a	n/a
36	BHLHE40	chr19:36336926-36337039	A549	lung:	n/a	n/a
37	BHLHE40	chr19:36334955-36335069	K562	blood:	n/a	n/a
38	BHLHE40	chr19:36347949-36347963	K562	blood:	n/a	n/a
39	BHLHE40	chr19:36360510-36360878	K562	blood:	n/a	n/a
40	BRCA1	chr19:36336261-36336523	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr19:36347497-36347930	H1-hESC	embryonic stem cell:	n/a	n/a
42	BRCA1	chr19:36360143-36360299	H1-hESC	embryonic stem cell:	n/a	n/a
43	BRCA1	chr19:36370618-36371046	Hela-S3	cervix:	n/a	n/a
44	CBX3	chr19:36353424-36353872	K562	blood:	n/a	n/a
45	CBX3	chr19:36370586-36371240	K562	blood:	n/a	n/a
46	CBX3	chr19:36336166-36336467	K562	blood:	n/a	n/a
47	CBX3	chr19:36360504-36360967	K562	blood:	n/a	n/a
48	CCNT2	chr19:36336223-36336585	K562	blood:	n/a	n/a
49	CCNT2	chr19:36346508-36346708	K562	blood:	n/a	chr19:36346671-36346680
50	CCNT2	chr19:36370655-36371019	K562	blood:	n/a	chr19:36370838-36370847

(count:3665 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:36359302-36359352	SKMC	muscle:	n/a
2	chr19:36332521-36332571	CMK	blood:	n/a
3	chr19:36343521-36343571	PrEC	prostate:	n/a
4	chr19:36347441-36347491	NT2-D1	testis:	n/a
5	chr19:36347626-36347676	HUVEC	blood vessel:	n/a
6	chr19:36359302-36359352	SKMC	muscle:	n/a
7	chr19:36332521-36332571	CMK	blood:	n/a
8	chr19:36343521-36343571	PrEC	prostate:	n/a
9	chr19:36347441-36347491	NT2-D1	testis:	n/a
10	chr19:36347626-36347676	HUVEC	blood vessel:	n/a
11	chr19:36360605-36360655	T-47D	breast:	n/a
12	chr19:36369620-36369670	HIPEpiC	eye:	n/a
13	chr19:36347919-36347969	NB4	blood:	n/a
14	chr19:36337033-36337083	PrEC	prostate:	n/a
15	chr19:36365307-36365357	GM12891	blood:	n/a
16	chr19:36359327-36359377	HL-60	blood:	n/a
17	chr19:36342859-36342909	PFSK-1	brain:	n/a
18	chr19:36352005-36352055	HUVEC	blood vessel:	n/a
19	chr19:36350479-36350529	HIPEpiC	eye:	n/a
20	chr19:36336620-36336670	HL-60	blood:	n/a
21	chr19:36351774-36351824	SK-N-SH	brain:	n/a
22	chr19:36357700-36357750	AG04450	lung:	fetal
23	chr19:36365679-36365729	HAEpiC	amniotic membrane:	n/a
24	chr19:36358783-36358833	HepG2	liver:	n/a
25	chr19:36342725-36342775	GM12892	blood:	n/a
26	chr19:36342859-36342909	HRPEpiC	eye:	n/a
27	chr19:36365307-36365357	GM12878	blood:	n/a
28	chr19:36359295-36359345	CMK	blood:	n/a
29	chr19:36360605-36360655	IMR90	lung:	fetal
30	chr19:36367330-36367380	MCF-7	breast:	n/a
31	chr19:36360489-36360539	GM19239	blood:	n/a
32	chr19:36347698-36347748	A549	lung:	n/a
33	chr19:36346314-36346364	AG04450	lung:	fetal
34	chr19:36343530-36343580	ovcar-3	ovarian:	n/a
35	chr19:36360489-36360539	U87	brain:	n/a
36	chr19:36360396-36360446	HRE	kidney:	n/a
37	chr19:36345675-36345725	HIPEpiC	eye:	n/a
38	chr19:36359772-36359822	Caco-2	colon:	n/a
39	chr19:36360834-36360884	HUVEC	blood vessel:	n/a
40	chr19:36352005-36352055	T-47D	breast:	n/a
41	chr19:36352459-36352509	IMR90	lung:	fetal
42	chr19:36347441-36347491	HepG2	liver:	n/a
43	chr19:36337308-36337358	HRCEpiC	kidney:	n/a
44	chr19:36347441-36347491	GM12892	blood:	n/a
45	chr19:36360396-36360446	Hepatocyte	liver:	n/a
46	chr19:36357115-36357165	GM12891	blood:	n/a
47	chr19:36360529-36360579	HMEC	breast:	n/a
48	chr19:36359283-36359333	SK-N-SH	brain:	n/a
49	chr19:36362894-36362944	NB4	blood:	n/a
50	chr19:36361866-36361916	NT2-D1	testis:	n/a

(count:71 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr19:36365053..36367604-chr19:36368904..36371843,2	MCF-7	breast:
2	chr19:36352312..36355033-chr19:36357971..36359905,3	MCF-7	breast:
3	chr19:36361275..36362791-chr19:36390518..36392697,2	K562	blood:
4	chr19:36335676..36337950-chr19:36339601..36341790,2	K562	blood:
5	chr19:36338551..36341228-chr19:36359496..36361624,3	K562	blood:
6	chr19:36346452..36348477-chr19:36350234..36352680,3	K562	blood:
7	chr19:36341339..36343391-chr19:36346097..36348874,2	MCF-7	breast:
8	chr19:36336450..36338602-chr19:36340290..36342312,2	K562	blood:
9	chr19:36370756..36373249-chr19:36545654..36547165,2	MCF-7	breast:
10	chr19:36336433..36337946-chr19:36338192..36339796,3	K562	blood:
11	chr19:36334818..36337477-chr19:36389378..36392350,2	MCF-7	breast:
12	chr19:36338551..36341228-chr19:36359496..36361624,3	K562	blood:
13	chr19:36333306..36335125-chr19:36337334..36339414,2	K562	blood:
14	chr19:36339670..36341868-chr19:36344808..36347697,2	MCF-7	breast:
15	chr19:36301268..36304054-chr19:36346309..36349120,2	K562	blood:
16	chr19:36342113..36343944-chr19:36344326..36346095,2	MCF-7	breast:
17	chr19:36235922..36238148-chr19:36359346..36361404,2	MCF-7	breast:
18	chr19:36339670..36341868-chr19:36344808..36347697,2	MCF-7	breast:
19	chr19:36352085..36353647-chr19:36356633..36358816,2	K562	blood:
20	chr19:36335712..36337227-chr19:36349133..36352127,2	MCF-7	breast:
21	chr19:36339201..36341036-chr19:36345575..36348442,2	K562	blood:
22	chr19:36348444..36350564-chr19:36358604..36360896,2	K562	blood:
23	chr19:36333824..36336431-chr19:36543842..36546200,2	MCF-7	breast:
24	chr19:36335780..36337313-chr19:36359455..36361667,2	MCF-7	breast:
25	chr19:36359272..36362126-chr19:36389056..36392231,3	MCF-7	breast:
26	chr19:36336403..36338756-chr19:36340642..36343905,3	MCF-7	breast:
27	chr19:36208185..36209878-chr19:36358146..36361161,3	K562	blood:
28	chr19:36336052..36339154-chr19:36344963..36347982,3	MCF-7	breast:
29	chr19:36358705..36361314-chr19:36484649..36486725,2	K562	blood:
30	chr19:36359598..36361922-chr19:36393124..36395167,2	K562	blood:
31	chr19:36365053..36367604-chr19:36368904..36371843,2	MCF-7	breast:
32	chr19:36208544..36210188-chr19:36360524..36362280,2	MCF-7	breast:
33	chr19:36352834..36355328-chr19:36359086..36361256,3	K562	blood:
34	chr19:36266549..36268656-chr19:36368007..36369573,2	K562	blood:
35	chr19:36363822..36367543-chr19:36368056..36371316,4	K562	blood:
36	chr19:36337442..36339208-chr19:36341974..36344339,2	K562	blood:
37	chr19:36352085..36353689-chr19:36356633..36358980,2	K562	blood:
38	chr19:36359256..36363302-chr19:36368429..36371554,3	K562	blood:
39	chr19:36339201..36341036-chr19:36345575..36348442,2	K562	blood:
40	chr19:36335676..36337950-chr19:36339601..36341790,2	K562	blood:
41	chr19:36274992..36277826-chr19:36328765..36330508,2	K562	blood:
42	chr19:36335744..36339702-chr19:36359166..36361673,6	MCF-7	breast:
43	chr19:36373464..36375910-chr19:36388053..36389740,2	K562	blood:
44	chr19:36335780..36337313-chr19:36359455..36361667,2	MCF-7	breast:
45	chr19:36370775..36373541-chr19:36425672..36427378,2	MCF-7	breast:
46	chr19:36335744..36339702-chr19:36359166..36361673,6	MCF-7	breast:
47	chr19:36208456..36210034-chr19:36345854..36347720,2	K562	blood:
48	chr19:36336052..36339154-chr19:36344963..36347982,3	MCF-7	breast:
49	chr19:36336450..36338602-chr19:36340290..36342312,2	K562	blood:
50	chr19:36208378..36210285-chr19:36358548..36361708,3	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NPHS1-3	chr19:36357389-36357495	NONHSAT065928
2	lnc-NPHS1-3	chr19:36359994-36360189	NONHSAT065928
3	lnc-NPHS1-3	chr19:36342553-36342574	NONHSAT065928
4	lnc-KIRREL2-3	chr19:36335144-36335402	NONHSAT065927
5	lnc-APLP1-1	chr19:36372792-36373053	NONHSAT065932
6	lnc-NFKBID-1	chr19:36372729-36372952	XLOC_013323
7	lnc-NFKBID-1	chr19:36375959-36376739	XLOC_013323
8	lnc-NFKBID-1	chr19:36370792-36371031	XLOC_013323
9	lnc-NPHS1-3	chr19:36358777-36359032	NONHSAT065928
10	lnc-KIRREL2-3	chr19:36336592-36336865	NONHSAT065927

No data

Variant related genes	Relation type
RN7SL402P	TF binding region
NPHS1	TF binding region
KIRREL2	TF binding region
APLP1	TF binding region
RN7SL402P	CpG island
NPHS1	CpG island
KIRREL2	CpG island
APLP1	CpG island
ENSG00000004776	chromatin interactions
ENSG00000126259	chromatin interactions
ENSG00000105290	chromatin interactions
ENSG00000167595	chromatin interactions
ENSG00000267796	chromatin interactions
ENSG00000267698	chromatin interactions
ENSG00000161265	chromatin interactions
ENSG00000126264	chromatin interactions
ENSG00000267439	chromatin interactions
ENSG00000161277	chromatin interactions
ENSG00000004777	chromatin interactions
ENSG00000267120	chromatin interactions
ENSG00000126243	chromatin interactions
ENSG00000272333	chromatin interactions
ENSG00000205138	chromatin interactions
ENSG00000161270	chromatin interactions
ENSG00000075702	chromatin interactions
ENSG00000188223	chromatin interactions
ENSG00000250799	chromatin interactions
ENSG00000205155	chromatin interactions
ENSG00000239382	chromatin interactions
ENSG00000167604	chromatin interactions

Extended variants
information (count: 2528 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:2528 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112969174	chr19:36326940-36326941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs112005760	chr19:36326947-36326948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs113955660	chr19:36326955-36326956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs2448262	chr19:36326972-36326973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs2448263	chr19:36326976-36326977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs386808956	chr19:36326986-36326987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs6510510	chr19:36326987-36326988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs369090944	chr19:36326989-36326990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs570374756	chr19:36326993-36326994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531151323	chr19:36326998-36326999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs8101253	chr19:36326999-36327000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545394756	chr19:36327005-36327006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs377235796	chr19:36327009-36327010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs368427492	chr19:36327010-36327011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs370657967	chr19:36327015-36327016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs77489574	chr19:36327016-36327017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs370392333	chr19:36327018-36327019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs373870766	chr19:36327019-36327020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs375593066	chr19:36327022-36327023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs371030303	chr19:36327024-36327025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs112247530	chr19:36327029-36327030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs7250674	chr19:36327051-36327052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs7246104	chr19:36327053-36327054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs373851105	chr19:36327057-36327058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374472090	chr19:36327068-36327069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs368395654	chr19:36327069-36327070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs79335088	chr19:36327077-36327078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372555110	chr19:36327080-36327081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs7246220	chr19:36327083-36327084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374506144	chr19:36327112-36327113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs577765153	chr19:36327152-36327153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs111517817	chr19:36327154-36327155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577656249	chr19:36327161-36327162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs576283911	chr19:36327271-36327272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543380691	chr19:36327272-36327273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs558896461	chr19:36327294-36327295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs117432109	chr19:36327321-36327322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs541490562	chr19:36327333-36327334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs559891554	chr19:36327351-36327352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs78257395	chr19:36327353-36327354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs141325529	chr19:36327358-36327359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs371387609	chr19:36327363-36327364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531217358	chr19:36327382-36327383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552608946	chr19:36327392-36327393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571191272	chr19:36327413-36327414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs532014465	chr19:36327420-36327421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183188416	chr19:36327459-36327460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs549055312	chr19:36327562-36327563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567434166	chr19:36327563-36327564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs368415016	chr19:36327615-36327616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	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
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Ovarian cancer	21397856	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Ovarian cancer	20844748	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Neurodevelopmental disorder	22521361	CNVD
Endometrial cancer	23636398	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Gastric cancer	21811585	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Glioma	17123091	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1850 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:36323200-36330000	Weak transcription	Pancreas	Pancrea
2	chr19:36330000-36330400	ZNF genes & repeats	Aorta	Aorta
3	chr19:36330000-36330400	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
4	chr19:36330000-36330400	ZNF genes & repeats	Pancreas	Pancrea
5	chr19:36330200-36330600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr19:36330400-36334600	Weak transcription	Pancreas	Pancrea
7	chr19:36330400-36336200	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr19:36332400-36334000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr19:36332600-36332800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr19:36333400-36333600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr19:36334000-36334200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr19:36334200-36336800	ZNF genes & repeats	Spleen	Spleen
13	chr19:36334400-36334800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
14	chr19:36334600-36334800	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
15	chr19:36334600-36334800	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
16	chr19:36334600-36335000	Bivalent/Poised TSS	A549	lung
17	chr19:36334600-36335200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
18	chr19:36334600-36335200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
19	chr19:36334600-36335400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
20	chr19:36334600-36335400	ZNF genes & repeats	Lung	lung
21	chr19:36334600-36335600	Enhancers	Pancreas	Pancrea
22	chr19:36334800-36335000	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr19:36334800-36335000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
24	chr19:36334800-36335000	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
25	chr19:36334800-36335000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr19:36334800-36335000	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr19:36334800-36335000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr19:36334800-36335000	Bivalent Enhancer	Brain Germinal Matrix	brain
29	chr19:36334800-36335000	Bivalent Enhancer	Esophagus	oesophagus
30	chr19:36334800-36335000	Bivalent Enhancer	Fetal Muscle Leg	muscle
31	chr19:36334800-36335200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
32	chr19:36334800-36335200	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr19:36334800-36335400	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
34	chr19:36334800-36335400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr19:36334800-36335400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr19:36334800-36335400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
37	chr19:36334800-36335400	Bivalent Enhancer	Right Ventricle	heart
38	chr19:36334800-36335600	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
39	chr19:36334800-36336000	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
40	chr19:36334800-36336000	Bivalent Enhancer	Brain Hippocampus Middle	brain
41	chr19:36334800-36336000	Bivalent Enhancer	Duodenum Mucosa	Duodenum
42	chr19:36334800-36336000	Enhancers	K562	blood
43	chr19:36334800-36336200	Bivalent Enhancer	Placenta	Placenta
44	chr19:36334800-36337400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
45	chr19:36334800-36337400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
46	chr19:36335000-36335200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr19:36335000-36335200	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
48	chr19:36335000-36335200	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
49	chr19:36335000-36335200	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
50	chr19:36335000-36335200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links