Variant report

Variant	nsv911642
Chromosome Location	chr19:36620778-36651499
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1346)
CpG islands
(count:1469)
Chromatin interactive
region (count:58)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1346 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:36630728-36631120	K562	blood:	n/a	n/a
2	ARID3A	chr19:36630542-36631057	HepG2	liver:	n/a	n/a
3	ATF2	chr19:36630483-36631209	GM12878	blood:	n/a	n/a
4	ATF2	chr19:36630687-36631128	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr19:36630699-36631185	K562	blood:	n/a	n/a
6	ATF3	chr19:36627570-36628569	A549	lung:	n/a	n/a
7	ATF3	chr19:36630658-36631045	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr19:36630769-36631116	K562	blood:	n/a	n/a
9	ATF3	chr19:36630272-36631259	A549	lung:	n/a	n/a
10	ATF3	chr19:36630130-36631481	A549	lung:	n/a	n/a
11	ATF3	chr19:36630710-36631110	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr19:36631989-36632696	A549	lung:	n/a	n/a
13	BACH1	chr19:36631334-36631848	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr19:36630353-36631126	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr19:36628136-36628270	K562	blood:	n/a	n/a
16	BACH1	chr19:36630298-36630890	K562	blood:	n/a	n/a
17	BACH1	chr19:36632323-36632586	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr19:36623412-36623619	GM12878	blood:	n/a	chr19:36623542-36623553
19	BATF	chr19:36647521-36647747	GM12878	blood:	n/a	n/a
20	BATF	chr19:36630412-36631143	GM12878	blood:	n/a	n/a
21	BCL3	chr19:36632007-36632680	A549	lung:	n/a	n/a
22	BCL3	chr19:36630076-36631337	A549	lung:	n/a	chr19:36630417-36630426
23	BCL3	chr19:36630064-36632006	A549	lung:	n/a	chr19:36631344-36631353 chr19:36630417-36630426
24	BCL3	chr19:36627469-36628580	A549	lung:	n/a	n/a
25	BCLAF1	chr19:36630357-36631194	GM12878	blood:	n/a	chr19:36630417-36630426
26	BHLHE40	chr19:36630287-36631156	GM12878	blood:	n/a	chr19:36630488-36630504 chr19:36630979-36630995 chr19:36631004-36631020
27	BHLHE40	chr19:36631732-36631828	GM12878	blood:	n/a	n/a
28	BHLHE40	chr19:36630416-36631031	A549	lung:	n/a	chr19:36630488-36630504 chr19:36630979-36630995 chr19:36631004-36631020
29	BHLHE40	chr19:36630285-36631266	K562	blood:	n/a	chr19:36630488-36630504 chr19:36630979-36630995 chr19:36631004-36631020
30	BHLHE40	chr19:36630418-36631103	HepG2	liver:	n/a	chr19:36630488-36630504 chr19:36630979-36630995 chr19:36631004-36631020
31	BRCA1	chr19:36630629-36630956	HepG2	liver:	n/a	n/a
32	BRCA1	chr19:36630650-36631022	H1-hESC	embryonic stem cell:	n/a	n/a
33	BRCA1	chr19:36630459-36631550	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr19:36630549-36631080	GM12878	blood:	n/a	n/a
35	CBX3	chr19:36623132-36624020	HCT-116	colon:	n/a	n/a
36	CBX3	chr19:36630127-36631153	K562	blood:	n/a	n/a
37	CBX3	chr19:36623264-36624034	HCT-116	colon:	n/a	n/a
38	CBX3	chr19:36630722-36631013	K562	blood:	n/a	n/a
39	CCNT2	chr19:36630347-36631234	K562	blood:	n/a	n/a
40	CEBPB	chr19:36622149-36622371	Hela-S3	cervix:	n/a	chr19:36622242-36622253
41	CEBPB	chr19:36630085-36631426	A549	lung:	n/a	n/a
42	CEBPB	chr19:36627800-36628258	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr19:36630787-36631195	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr19:36622043-36622414	ECC-1	luminal epithelium:	n/a	chr19:36622242-36622253
45	CEBPB	chr19:36645017-36645241	IMR90	lung:	n/a	n/a
46	CEBPB	chr19:36630330-36631652	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr19:36623333-36623863	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr19:36645637-36645663	A549	lung:	n/a	n/a
49	CEBPB	chr19:36630816-36631001	HepG2	liver:	n/a	n/a
50	CEBPB	chr19:36630481-36630525	K562	blood:	n/a	n/a

(count:1469 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:36643572-36643622	AG10803	skin:	n/a
2	chr19:36644277-36644327	BJ	skin:	n/a
3	chr19:36631141-36631191	HepG2	liver:	n/a
4	chr19:36631318-36631368	PFSK-1	brain:	n/a
5	chr19:36643572-36643622	IMR90	lung:	fetal
6	chr19:36643572-36643622	AG10803	skin:	n/a
7	chr19:36644277-36644327	BJ	skin:	n/a
8	chr19:36631141-36631191	HepG2	liver:	n/a
9	chr19:36631318-36631368	PFSK-1	brain:	n/a
10	chr19:36643572-36643622	IMR90	lung:	fetal
11	chr19:36631318-36631368	Hela-S3	cervix:	n/a
12	chr19:36630557-36630607	Hepatocyte	liver:	n/a
13	chr19:36630888-36630938	PFSK-1	brain:	n/a
14	chr19:36640758-36640808	BJ	skin:	n/a
15	chr19:36630627-36630677	IMR90	lung:	fetal
16	chr19:36630902-36630952	T-47D	breast:	n/a
17	chr19:36630914-36630964	AoSMC	blood vessel:	n/a
18	chr19:36642720-36642770	AG04449	skin:	fetal
19	chr19:36630902-36630952	HAEpiC	amniotic membrane:	n/a
20	chr19:36633207-36633257	GM12892	blood:	n/a
21	chr19:36631141-36631191	PANC-1	pancreas:	n/a
22	chr19:36630627-36630677	Hela-S3	cervix:	n/a
23	chr19:36630888-36630938	PrEC	prostate:	n/a
24	chr19:36640758-36640808	GM19239	blood:	n/a
25	chr19:36633207-36633257	HCPEpiC	choroid plexus:	n/a
26	chr19:36627324-36627374	U87	brain:	n/a
27	chr19:36633207-36633257	GM06990	blood:	n/a
28	chr19:36644751-36644801	HIPEpiC	eye:	n/a
29	chr19:36644277-36644327	LNCaP	prostate:	n/a
30	chr19:36621529-36621579	GM19239	blood:	n/a
31	chr19:36630602-36630652	U87	brain:	n/a
32	chr19:36631058-36631108	NT2-D1	testis:	n/a
33	chr19:36642720-36642770	HNPCEpiC	eye:	n/a
34	chr19:36638843-36638893	NB4	blood:	n/a
35	chr19:36633213-36633263	AG09319	gingival:	n/a
36	chr19:36643572-36643622	SK-N-SH	brain:	n/a
37	chr19:36630914-36630964	GM19239	blood:	n/a
38	chr19:36638843-36638893	SKMC	muscle:	n/a
39	chr19:36644277-36644327	SKMC	muscle:	n/a
40	chr19:36638843-36638893	HepG2	liver:	n/a
41	chr19:36630602-36630652	HUVEC	blood vessel:	n/a
42	chr19:36630882-36630932	H1-hESC	embryonic stem cell:	embryo
43	chr19:36630557-36630607	K562	blood:	n/a
44	chr19:36643070-36643120	HEK293	kidney:	embryo
45	chr19:36630902-36630952	A549	lung:	n/a
46	chr19:36627324-36627374	SK-N-SH_RA	brain:	n/a
47	chr19:36643771-36643821	HAEpiC	amniotic membrane:	n/a
48	chr19:36644751-36644801	SK-N-MC	brain:	n/a
49	chr19:36633213-36633263	AG04450	lung:	fetal
50	chr19:36630914-36630964	GM12878	blood:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr19:36602524..36605915-chr19:36624764..36627980,3	MCF-7	breast:
2	chr19:36630769..36631425-chr3:57678429..57679174,2	Hela-S3	cervix:
3	chr17:80416314..80417083-chr19:36630660..36631409,2	Hela-S3	cervix:
4	chr19:36630738..36632299-chr19:36705733..36707758,2	MCF-7	breast:
5	chr19:36618864..36621054-chr19:36633673..36635614,2	MCF-7	breast:
6	chr17:16283924..16284578-chr19:36631010..36631547,2	Hela-S3	cervix:
7	chr19:36617223..36621168-chr19:36621174..36623571,4	MCF-7	breast:
8	chr19:36612874..36616073-chr19:36617819..36620812,3	MCF-7	breast:
9	chr19:36624813..36626447-chr19:36704733..36707629,2	K562	blood:
10	chr19:36607813..36612546-chr19:36618709..36622770,5	MCF-7	breast:
11	chr19:36630678..36632307-chr19:36642468..36644265,2	K562	blood:
12	chr19:36604314..36608037-chr19:36629557..36633745,12	MCF-7	breast:
13	chr19:36630602..36632414-chr19:38875371..38878496,3	MCF-7	breast:
14	chr19:36627567..36628266-chr3:119813840..119814541,2	Hela-S3	cervix:
15	chr19:36630678..36632307-chr19:36642468..36644265,2	K562	blood:
16	chr19:36630278..36632151-chr19:36704046..36706551,3	MCF-7	breast:
17	chr1:228400809..228401396-chr19:36631414..36632120,2	Hela-S3	cervix:
18	chr10:120840114..120840715-chr19:36630815..36631334,2	Hela-S3	cervix:
19	chr19:36635772..36637555-chr19:36705789..36707718,2	K562	blood:
20	chr19:36618936..36620566-chr19:36620843..36623517,2	MCF-7	breast:
21	chr19:36636671..36639034-chr19:36695235..36696837,2	K562	blood:
22	chr19:36544760..36547180-chr19:36619218..36620839,2	MCF-7	breast:
23	chr19:36615077..36620423-chr19:36622100..36624907,6	K562	blood:
24	chr19:36604594..36608993-chr19:36628830..36633466,13	K562	blood:
25	chr19:36617223..36621168-chr19:36621174..36623571,4	MCF-7	breast:
26	chr19:36621233..36623122-chr19:37063921..37066153,2	K562	blood:
27	chr10:94352936..94353453-chr19:36630960..36631661,2	Hela-S3	cervix:
28	chr19:36618747..36620839-chr19:36626381..36628843,2	K562	blood:
29	chr19:36629161..36631921-chr19:37341375..37343285,2	MCF-7	breast:
30	chr19:36618747..36620839-chr19:36626381..36628843,2	K562	blood:
31	chr19:36543201..36546500-chr19:36630161..36633757,3	MCF-7	breast:
32	chr16:29936944..29937902-chr19:36630893..36631603,2	Hela-S3	cervix:
33	chr19:36548167..36550367-chr19:36618997..36621964,2	MCF-7	breast:
34	chr12:96793870..96794769-chr19:36631076..36631914,2	Hela-S3	cervix:
35	chr19:36605008..36606623-chr19:36627761..36629746,2	K562	blood:
36	chr19:36628146..36630638-chr19:37017222..37019646,2	K562	blood:
37	chr19:36617250..36625256-chr19:36625801..36633837,31	MCF-7	breast:
38	chr17:40828184..40828848-chr19:36631342..36632165,2	Hela-S3	cervix:
39	chr19:36601521..36604291-chr19:36630338..36633807,8	MCF-7	breast:
40	chr13:38923439..38924342-chr19:36630421..36631091,2	Hela-S3	cervix:
41	chr19:36643816..36646322-chr19:36651862..36654604,2	K562	blood:
42	chr19:36630738..36632588-chr19:36651026..36652754,2	MCF-7	breast:
43	chr19:36630683..36631317-chr22:43010387..43011247,2	Hela-S3	cervix:
44	chr19:36630466..36632159-chr19:36704253..36707369,3	K562	blood:
45	chr19:36635447..36638773-chr19:36641889..36645478,3	K562	blood:
46	chr19:36635447..36638773-chr19:36641889..36645478,3	K562	blood:
47	chr19:36604617..36608522-chr19:36628102..36632329,9	MCF-7	breast:
48	chr19:36604026..36607708-chr19:36630473..36633466,10	K562	blood:
49	chr19:36629391..36631341-chr19:38851035..38853209,2	MCF-7	breast:
50	chr19:36636004..36639367-chr19:36650877..36653820,3	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COX7A1-2	chr19:36634983-36635051	ENSG00000270760.1
2	lnc-CAPNS1-2	chr19:36646018-36647113	NONHSAT065965
3	lnc-COX7A1-2	chr19:36638941-36639250	ENSG00000270760.1
4	lnc-CAPNS1-1	chr19:36644712-36645101	NONHSAT065964

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CAPNS1	hsa-miR-124-3p	chr19:36641168-36641188
2	CAPNS1	hsa-miR-124-3p	chr19:36641181-36641187

Variant related genes	Relation type
COX7A1	TF binding region
ENSG00000270760	TF binding region
CAPNS1	TF binding region
COX7A1	CpG island
ENSG00000270760	CpG island
CAPNS1	CpG island
ENSG00000075702	chromatin interactions
ENSG00000196357	chromatin interactions
ENSG00000059758	chromatin interactions
ENSG00000068137	chromatin interactions
ENSG00000161281	chromatin interactions
ENSG00000265458	chromatin interactions
ENSG00000266963	chromatin interactions
ENSG00000241933	chromatin interactions
ENSG00000186020	chromatin interactions
ENSG00000105254	chromatin interactions
ENSG00000251247	chromatin interactions
ENSG00000170315	chromatin interactions
ENSG00000267090	chromatin interactions
ENSG00000100227	chromatin interactions
ENSG00000233527	chromatin interactions
ENSG00000242622	chromatin interactions
ENSG00000120686	chromatin interactions
ENSG00000138160	chromatin interactions
ENSG00000254004	chromatin interactions
ENSG00000105261	chromatin interactions
ENSG00000174943	chromatin interactions
ENSG00000105258	chromatin interactions
ENSG00000167604	chromatin interactions
ENSG00000162913	chromatin interactions
ENSG00000126247	chromatin interactions
ENSG00000167642	chromatin interactions
ENSG00000270760	chromatin interactions
ENSG00000141562	chromatin interactions
ENSG00000161277	chromatin interactions
ENSG00000197863	chromatin interactions
ENSG00000174839	chromatin interactions
ENSG00000167635	chromatin interactions
ENSG00000107581	chromatin interactions
ENSG00000182831	chromatin interactions
ENSG00000228629	chromatin interactions

Extended variants
information (count: 1338 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1338 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16970889	chr19:36620778-36620779	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs181740513	chr19:36620854-36620855	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs550127369	chr19:36620855-36620856	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs559587300	chr19:36620901-36620902	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs569621277	chr19:36620908-36620909	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs538790167	chr19:36620965-36620966	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs530163189	chr19:36620980-36620981	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs148671432	chr19:36620985-36620986	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs563873857	chr19:36620986-36620987	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs76300049	chr19:36621003-36621004	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs552882955	chr19:36621031-36621032	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs571197631	chr19:36621064-36621065	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs566141865	chr19:36621068-36621069	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs532136910	chr19:36621235-36621236	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs186092665	chr19:36621299-36621300	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs565548476	chr19:36621414-36621415	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs199922269	chr19:36621426-36621427	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs529685191	chr19:36621446-36621447	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs548000695	chr19:36621463-36621464	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs377394767	chr19:36621534-36621535	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs57185996	chr19:36621544-36621545	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs138240312	chr19:36621569-36621570	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs536877087	chr19:36621642-36621643	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs12977802	chr19:36621643-36621644	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs566696135	chr19:36621704-36621705	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs376154649	chr19:36621729-36621730	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs533950267	chr19:36621766-36621767	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs576771791	chr19:36621771-36621772	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs76506198	chr19:36621778-36621779	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs368455766	chr19:36621791-36621792	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs115047713	chr19:36621864-36621865	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs574758784	chr19:36621890-36621891	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs542283828	chr19:36621954-36621955	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs151232152	chr19:36621961-36621962	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs76082019	chr19:36621975-36621976	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs546460411	chr19:36621979-36621980	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs564767068	chr19:36621988-36621989	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs373874438	chr19:36622063-36622064	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs552405381	chr19:36622065-36622066	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs115800703	chr19:36622080-36622081	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs2141959	chr19:36622098-36622099	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs189482324	chr19:36622101-36622102	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs139418113	chr19:36622109-36622110	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs9917031	chr19:36622147-36622148	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs79182966	chr19:36622152-36622153	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs143953906	chr19:36622181-36622182	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs116219283	chr19:36622194-36622195	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs570324050	chr19:36622208-36622209	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs556720067	chr19:36622216-36622217	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs115562939	chr19:36622226-36622227	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

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

Chromatin state (count:1590 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:36618400-36621000	Enhancers	Stomach Mucosa	stomach
2	chr19:36619600-36622600	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr19:36619600-36622800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr19:36619600-36622800	Weak transcription	Lung	lung
5	chr19:36619600-36623400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr19:36619600-36623400	Weak transcription	Gastric	stomach
7	chr19:36619600-36623400	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr19:36619600-36627600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr19:36619600-36630200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr19:36619800-36621600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr19:36619800-36621600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr19:36619800-36621600	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr19:36619800-36622000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr19:36619800-36622000	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr19:36619800-36622000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr19:36619800-36622000	Weak transcription	Adipose Nuclei	Adipose
17	chr19:36619800-36622200	Weak transcription	Primary B cells from cord blood	blood
18	chr19:36619800-36622400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr19:36619800-36622400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr19:36619800-36622600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
21	chr19:36619800-36622600	Weak transcription	HMEC	breast
22	chr19:36619800-36622600	Weak transcription	NHEK	skin
23	chr19:36619800-36623000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr19:36619800-36623200	Weak transcription	Primary T helper cells PMA-I stimulated	--
25	chr19:36619800-36623400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr19:36619800-36623400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr19:36619800-36623400	Weak transcription	Primary T cells from cord blood	blood
28	chr19:36619800-36623400	Weak transcription	GM12878-XiMat	blood
29	chr19:36619800-36623400	Weak transcription	HUVEC	blood vessel
30	chr19:36619800-36623400	Weak transcription	NH-A	brain
31	chr19:36619800-36623600	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr19:36619800-36624400	Enhancers	Placenta	Placenta
33	chr19:36619800-36624600	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr19:36619800-36627200	Weak transcription	HUES6 Cell Line	embryonic stem cell
35	chr19:36619800-36627200	Weak transcription	Duodenum Mucosa	Duodenum
36	chr19:36619800-36627600	Weak transcription	Colon Smooth Muscle	Colon
37	chr19:36619800-36627600	Weak transcription	Right Atrium	heart
38	chr19:36619800-36627600	Weak transcription	Osteobl	bone
39	chr19:36619800-36627800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
40	chr19:36619800-36627800	Weak transcription	Fetal Muscle Leg	muscle
41	chr19:36619800-36630000	Weak transcription	Fetal Thymus	thymus
42	chr19:36619800-36630200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr19:36620000-36621800	Weak transcription	Primary B cells from peripheral blood	blood
44	chr19:36620000-36621800	Weak transcription	Primary T cells fromperipheralblood	blood
45	chr19:36620000-36622000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr19:36620000-36622000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr19:36620000-36622600	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr19:36620000-36622800	Weak transcription	Skeletal Muscle Male	skeletal muscle
49	chr19:36620000-36623200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr19:36620000-36623400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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