Variant report

Variant	nsv911643
Chromosome Location	chr19:36627790-36651499
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1222)
CpG islands
(count:1344)
Chromatin interactive
region (count:44)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:36630542-36631057	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:36630728-36631120	K562	blood:	n/a	n/a
3	ATF2	chr19:36630687-36631128	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr19:36630483-36631209	GM12878	blood:	n/a	n/a
5	ATF3	chr19:36631989-36632696	A549	lung:	n/a	n/a
6	ATF3	chr19:36630272-36631259	A549	lung:	n/a	n/a
7	ATF3	chr19:36630710-36631110	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr19:36627570-36628569	A549	lung:	n/a	n/a
9	ATF3	chr19:36630769-36631116	K562	blood:	n/a	n/a
10	ATF3	chr19:36630658-36631045	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr19:36630699-36631185	K562	blood:	n/a	n/a
12	ATF3	chr19:36630130-36631481	A549	lung:	n/a	n/a
13	BACH1	chr19:36631334-36631848	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr19:36632323-36632586	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr19:36628136-36628270	K562	blood:	n/a	n/a
16	BACH1	chr19:36630353-36631126	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr19:36630298-36630890	K562	blood:	n/a	n/a
18	BATF	chr19:36630412-36631143	GM12878	blood:	n/a	n/a
19	BATF	chr19:36647521-36647747	GM12878	blood:	n/a	n/a
20	BCL3	chr19:36632007-36632680	A549	lung:	n/a	n/a
21	BCL3	chr19:36627469-36628580	A549	lung:	n/a	n/a
22	BCL3	chr19:36630064-36632006	A549	lung:	n/a	chr19:36631344-36631353 chr19:36630417-36630426
23	BCL3	chr19:36630076-36631337	A549	lung:	n/a	chr19:36630417-36630426
24	BCLAF1	chr19:36630357-36631194	GM12878	blood:	n/a	chr19:36630417-36630426
25	BHLHE40	chr19:36630287-36631156	GM12878	blood:	n/a	chr19:36630488-36630504 chr19:36630979-36630995 chr19:36631004-36631020
26	BHLHE40	chr19:36630285-36631266	K562	blood:	n/a	chr19:36630488-36630504 chr19:36630979-36630995 chr19:36631004-36631020
27	BHLHE40	chr19:36630416-36631031	A549	lung:	n/a	chr19:36630488-36630504 chr19:36630979-36630995 chr19:36631004-36631020
28	BHLHE40	chr19:36630418-36631103	HepG2	liver:	n/a	chr19:36630488-36630504 chr19:36630979-36630995 chr19:36631004-36631020
29	BHLHE40	chr19:36631732-36631828	GM12878	blood:	n/a	n/a
30	BRCA1	chr19:36630549-36631080	GM12878	blood:	n/a	n/a
31	BRCA1	chr19:36630650-36631022	H1-hESC	embryonic stem cell:	n/a	n/a
32	BRCA1	chr19:36630629-36630956	HepG2	liver:	n/a	n/a
33	BRCA1	chr19:36630459-36631550	Hela-S3	cervix:	n/a	n/a
34	CBX3	chr19:36630127-36631153	K562	blood:	n/a	n/a
35	CBX3	chr19:36630722-36631013	K562	blood:	n/a	n/a
36	CCNT2	chr19:36630347-36631234	K562	blood:	n/a	n/a
37	CEBPB	chr19:36630816-36631001	HepG2	liver:	n/a	n/a
38	CEBPB	chr19:36645637-36645663	A549	lung:	n/a	n/a
39	CEBPB	chr19:36627800-36628258	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr19:36630330-36631652	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr19:36630481-36630525	K562	blood:	n/a	n/a
42	CEBPB	chr19:36645017-36645241	IMR90	lung:	n/a	n/a
43	CEBPB	chr19:36630085-36631426	A549	lung:	n/a	n/a
44	CEBPB	chr19:36630787-36631195	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPD	chr19:36630720-36631166	K562	blood:	n/a	n/a
46	CEBPD	chr19:36630476-36631243	HepG2	liver:	n/a	n/a
47	CHD1	chr19:36631110-36631120	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD1	chr19:36630264-36631277	GM12878	blood:	n/a	n/a
49	CHD1	chr19:36631499-36631890	GM12878	blood:	n/a	n/a
50	CHD2	chr19:36630455-36631186	K562	blood:	n/a	n/a

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:36631318-36631368	LNCaP	prostate:	n/a
2	chr19:36633213-36633263	HL-60	blood:	n/a
3	chr19:36631318-36631368	LNCaP	prostate:	n/a
4	chr19:36633213-36633263	HL-60	blood:	n/a
5	chr19:36630882-36630932	K562	blood:	n/a
6	chr19:36633213-36633263	AG09319	gingival:	n/a
7	chr19:36630627-36630677	HepG2	liver:	n/a
8	chr19:36644751-36644801	HepG2	liver:	n/a
9	chr19:36643572-36643622	NHDF-neo	bronchial:	n/a
10	chr19:36630602-36630652	HAEpiC	amniotic membrane:	n/a
11	chr19:36631074-36631124	K562	blood:	n/a
12	chr19:36631141-36631191	SK-N-SH_RA	brain:	n/a
13	chr19:36642720-36642770	Hela-S3	cervix:	n/a
14	chr19:36630914-36630964	SK-N-SH_RA	brain:	n/a
15	chr19:36640758-36640808	Caco-2	colon:	n/a
16	chr19:36630914-36630964	BE2_C	brain:	n/a
17	chr19:36630602-36630652	U87	brain:	n/a
18	chr19:36640758-36640808	NT2-D1	testis:	n/a
19	chr19:36630557-36630607	A549	lung:	n/a
20	chr19:36631058-36631108	AG10803	skin:	n/a
21	chr19:36630627-36630677	SAEC	small airway:	n/a
22	chr19:36630557-36630607	ECC-1	luminal epithelium:	n/a
23	chr19:36631074-36631124	HRE	kidney:	n/a
24	chr19:36638843-36638893	HPAEpiC	pulmonary alveolar:	n/a
25	chr19:36644277-36644327	BJ	skin:	n/a
26	chr19:36630914-36630964	RPTEC	kidney:	n/a
27	chr19:36638843-36638893	GM12891	blood:	n/a
28	chr19:36644277-36644327	HAEpiC	amniotic membrane:	n/a
29	chr19:36630882-36630932	Jurkat	blood:	n/a
30	chr19:36629608-36629658	GM12892	blood:	n/a
31	chr19:36643572-36643622	PANC-1	pancreas:	n/a
32	chr19:36633213-36633263	T-47D	breast:	n/a
33	chr19:36631318-36631368	HPAEpiC	pulmonary alveolar:	n/a
34	chr19:36630902-36630952	NHBE	bronchial:	n/a
35	chr19:36630882-36630932	BJ	skin:	n/a
36	chr19:36630882-36630932	AG04449	skin:	fetal
37	chr19:36631058-36631108	Jurkat	blood:	n/a
38	chr19:36630557-36630607	HCM	heart:	n/a
39	chr19:36643572-36643622	U87	brain:	n/a
40	chr19:36643771-36643821	K562	blood:	n/a
41	chr19:36630557-36630607	PFSK-1	brain:	n/a
42	chr19:36643572-36643622	H1-hESC	embryonic stem cell:	embryo
43	chr19:36630557-36630607	HUVEC	blood vessel:	n/a
44	chr19:36630888-36630938	PANC-1	pancreas:	n/a
45	chr19:36644277-36644327	SKMC	muscle:	n/a
46	chr19:36633207-36633257	HepG2	liver:	n/a
47	chr19:36633213-36633263	SKMC	muscle:	n/a
48	chr19:36631058-36631108	MCF-7	breast:	n/a
49	chr19:36631141-36631191	AG04449	skin:	fetal
50	chr19:36631074-36631124	BE2_C	brain:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:36627567..36628266-chr3:119813840..119814541,2	Hela-S3	cervix:
2	chr19:36629391..36631341-chr19:38851035..38853209,2	MCF-7	breast:
3	chr19:36630602..36632414-chr19:38875371..38878496,3	MCF-7	breast:
4	chr19:36543278..36547003-chr19:36629856..36633093,3	MCF-7	breast:
5	chr19:36630738..36632588-chr19:36651026..36652754,2	MCF-7	breast:
6	chr19:36618864..36621054-chr19:36633673..36635614,2	MCF-7	breast:
7	chr19:36605008..36606623-chr19:36627761..36629746,2	K562	blood:
8	chr13:38923439..38924342-chr19:36630421..36631091,2	Hela-S3	cervix:
9	chr10:120840114..120840715-chr19:36630815..36631334,2	Hela-S3	cervix:
10	chr19:36630683..36631317-chr22:43010387..43011247,2	Hela-S3	cervix:
11	chr19:36618747..36620839-chr19:36626381..36628843,2	K562	blood:
12	chr19:36604617..36608522-chr19:36628102..36632329,9	MCF-7	breast:
13	chr16:29936944..29937902-chr19:36630893..36631603,2	Hela-S3	cervix:
14	chr19:36636004..36639367-chr19:36650877..36653820,3	K562	blood:
15	chr19:36602524..36605915-chr19:36624764..36627980,3	MCF-7	breast:
16	chr19:36604594..36608993-chr19:36628830..36633466,13	K562	blood:
17	chr19:36604314..36608037-chr19:36629557..36633745,12	MCF-7	breast:
18	chr19:36635447..36638773-chr19:36641889..36645478,3	K562	blood:
19	chr19:36630466..36632159-chr19:36704253..36707369,3	K562	blood:
20	chr17:80416314..80417083-chr19:36630660..36631409,2	Hela-S3	cervix:
21	chr19:36630769..36631425-chr3:57678429..57679174,2	Hela-S3	cervix:
22	chr17:40828184..40828848-chr19:36631342..36632165,2	Hela-S3	cervix:
23	chr19:36635447..36638773-chr19:36641889..36645478,3	K562	blood:
24	chr19:36635772..36637555-chr19:36705789..36707718,2	K562	blood:
25	chr19:36630678..36632307-chr19:36642468..36644265,2	K562	blood:
26	chr19:36601521..36604291-chr19:36630338..36633807,8	MCF-7	breast:
27	chr16:9185392..9186090-chr19:36630875..36631576,2	Hela-S3	cervix:
28	chr10:94352936..94353453-chr19:36630960..36631661,2	Hela-S3	cervix:
29	chr19:36643816..36646322-chr19:36651862..36654604,2	K562	blood:
30	chr19:36636671..36639034-chr19:36695235..36696837,2	K562	blood:
31	chr19:36604026..36607708-chr19:36630473..36633466,10	K562	blood:
32	chr17:16283924..16284578-chr19:36631010..36631547,2	Hela-S3	cervix:
33	chr19:36630678..36632307-chr19:36642468..36644265,2	K562	blood:
34	chr19:36391220..36392948-chr19:36631072..36632593,2	MCF-7	breast:
35	chr19:36630278..36632151-chr19:36704046..36706551,3	MCF-7	breast:
36	chr19:36629161..36631921-chr19:37341375..37343285,2	MCF-7	breast:
37	chr19:36543201..36546500-chr19:36630161..36633757,3	MCF-7	breast:
38	chr19:36544655..36547364-chr19:36630776..36632492,2	K562	blood:
39	chr19:36628146..36630638-chr19:37017222..37019646,2	K562	blood:
40	chr12:96793870..96794769-chr19:36631076..36631914,2	Hela-S3	cervix:
41	chr1:228400809..228401396-chr19:36631414..36632120,2	Hela-S3	cervix:
42	chr19:36629887..36633258-chr19:36704150..36708473,10	K562	blood:
43	chr19:36630738..36632299-chr19:36705733..36707758,2	MCF-7	breast:
44	chr19:36629466..36631434-chr19:38753724..38756328,2	MCF-7	breast:

(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-CAPNS1-1	chr19:36644712-36645101	NONHSAT065964
4	lnc-COX7A1-2	chr19:36638941-36639250	ENSG00000270760.1

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
ENSG00000120686	chromatin interactions
ENSG00000251247	chromatin interactions
ENSG00000161277	chromatin interactions
ENSG00000167635	chromatin interactions
ENSG00000197863	chromatin interactions
ENSG00000162913	chromatin interactions
ENSG00000167642	chromatin interactions
ENSG00000167604	chromatin interactions
ENSG00000241933	chromatin interactions
ENSG00000105261	chromatin interactions
ENSG00000068137	chromatin interactions
ENSG00000141562	chromatin interactions
ENSG00000170315	chromatin interactions
ENSG00000105254	chromatin interactions
ENSG00000126247	chromatin interactions
ENSG00000242622	chromatin interactions
ENSG00000182831	chromatin interactions
ENSG00000161281	chromatin interactions
ENSG00000267090	chromatin interactions
ENSG00000228629	chromatin interactions
ENSG00000174839	chromatin interactions
ENSG00000270760	chromatin interactions
ENSG00000107581	chromatin interactions
ENSG00000059758	chromatin interactions
ENSG00000196357	chromatin interactions
ENSG00000075702	chromatin interactions
ENSG00000174943	chromatin interactions
ENSG00000265458	chromatin interactions
ENSG00000254004	chromatin interactions
ENSG00000266963	chromatin interactions
ENSG00000138160	chromatin interactions
ENSG00000105258	chromatin interactions
ENSG00000100227	chromatin interactions

Extended variants
information (count: 1075 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1075 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10410162	chr19:36627790-36627791	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs113333979	chr19:36627792-36627793	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs547456530	chr19:36627824-36627825	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs553876312	chr19:36627935-36627936	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs565682182	chr19:36627950-36627951	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs535944705	chr19:36627973-36627974	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs547938550	chr19:36627998-36627999	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs569528656	chr19:36628044-36628045	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs572059231	chr19:36628097-36628098	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs536920194	chr19:36628180-36628181	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs558607120	chr19:36628199-36628200	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs570807970	chr19:36628204-36628205	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs10403192	chr19:36628330-36628331	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs553429505	chr19:36628357-36628358	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs574940869	chr19:36628359-36628360	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs542352425	chr19:36628378-36628379	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs146232113	chr19:36628400-36628401	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs185766872	chr19:36628452-36628453	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs7251374	chr19:36628463-36628464	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs374191374	chr19:36628473-36628474	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs373063153	chr19:36628511-36628512	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs564325508	chr19:36628566-36628567	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs576426142	chr19:36628570-36628571	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs543567715	chr19:36628573-36628574	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs138059777	chr19:36628589-36628590	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs564663466	chr19:36628603-36628604	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs532126301	chr19:36628627-36628628	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs540620662	chr19:36628634-36628635	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs561717917	chr19:36628637-36628638	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs559307578	chr19:36628646-36628647	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs190138675	chr19:36628672-36628673	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs117202554	chr19:36628685-36628686	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs569491126	chr19:36628716-36628717	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs530652432	chr19:36628757-36628758	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs573575520	chr19:36628763-36628764	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs552436049	chr19:36628845-36628846	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs550944524	chr19:36628882-36628883	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs3028991	chr19:36628905-36628906	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs67853589	chr19:36628906-36628907	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs182404967	chr19:36628919-36628920	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs10523649	chr19:36628924-36628925	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs376945476	chr19:36628925-36628926	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs185939874	chr19:36628930-36628931	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs553052137	chr19:36629004-36629005	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs568481483	chr19:36629009-36629010	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs375019912	chr19:36629011-36629012	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs190601942	chr19:36629034-36629035	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs142663754	chr19:36629062-36629063	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs2091825	chr19:36629101-36629102	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs56909282	chr19:36629129-36629130	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:1417 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:36619600-36630200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr19:36619800-36627800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr19:36619800-36627800	Weak transcription	Fetal Muscle Leg	muscle
4	chr19:36619800-36630000	Weak transcription	Fetal Thymus	thymus
5	chr19:36619800-36630200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr19:36622600-36629800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr19:36623600-36630200	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr19:36623600-36630200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr19:36623800-36629600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr19:36623800-36630400	Weak transcription	Lung	lung
11	chr19:36624000-36630200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr19:36624200-36630200	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr19:36624600-36627800	Weak transcription	Spleen	Spleen
14	chr19:36624600-36629600	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr19:36624600-36630000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr19:36625800-36627800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr19:36626200-36628800	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr19:36626200-36629600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr19:36626600-36630200	Weak transcription	Right Ventricle	heart
20	chr19:36626600-36630400	Weak transcription	Esophagus	oesophagus
21	chr19:36626600-36630400	Weak transcription	Gastric	stomach
22	chr19:36626800-36628400	Enhancers	Muscle Satellite Cultured Cells	--
23	chr19:36627000-36628200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr19:36627000-36628200	Enhancers	K562	blood
25	chr19:36627000-36628600	Enhancers	Stomach Mucosa	stomach
26	chr19:36627200-36627800	Enhancers	Colonic Mucosa	Colon
27	chr19:36627200-36628000	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr19:36627200-36628200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr19:36627200-36628200	Enhancers	Placenta	Placenta
30	chr19:36627200-36628200	Enhancers	Placenta Amnion	Placenta Amnion
31	chr19:36627200-36628200	Flanking Active TSS	Hela-S3	cervix
32	chr19:36627200-36628400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr19:36627200-36628400	Enhancers	HUVEC	blood vessel
34	chr19:36627200-36628400	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr19:36627400-36627800	Active TSS	HepG2	liver
36	chr19:36627400-36628200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr19:36627400-36628200	Flanking Active TSS	NHEK	skin
38	chr19:36627600-36627800	Active TSS	Duodenum Smooth Muscle	Duodenum
39	chr19:36627600-36627800	Active TSS	Rectal Smooth Muscle	rectum
40	chr19:36627600-36628000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr19:36627600-36628000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr19:36627600-36628000	Flanking Active TSS	Duodenum Mucosa	Duodenum
43	chr19:36627600-36628000	Enhancers	Left Ventricle	heart
44	chr19:36627600-36628000	Enhancers	Sigmoid Colon	Sigmoid Colon
45	chr19:36627600-36628000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
46	chr19:36627600-36628000	Flanking Active TSS	Stomach Smooth Muscle	stomach
47	chr19:36627600-36628000	Flanking Active TSS	HMEC	breast
48	chr19:36627600-36628000	Flanking Active TSS	HSMM	muscle
49	chr19:36627600-36628000	Flanking Active TSS	HSMMtube	muscle
50	chr19:36627600-36628000	Flanking Active TSS	Osteobl	bone

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