Variant report

Variant	nsv1046526
Chromosome Location	chr14:32110537-32567426
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4785)
CpG islands
(count:1710)
Chromatin interactive
region (count:136)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:4785 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:32552576-32553877	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:32542785-32543194	K562	blood:	n/a	n/a
3	ARID3A	chr14:32435269-32435821	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:32406936-32407273	K562	blood:	n/a	n/a
5	ARID3A	chr14:32546566-32546731	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:32153639-32153640	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:32256644-32256965	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:32547232-32548836	HepG2	liver:	n/a	n/a
9	ARID3A	chr14:32364687-32364887	HepG2	liver:	n/a	n/a
10	ARID3A	chr14:32479723-32480057	K562	blood:	n/a	n/a
11	ARID3A	chr14:32399791-32399991	HepG2	liver:	n/a	n/a
12	ARID3A	chr14:32545442-32546356	HepG2	liver:	n/a	n/a
13	ARID3A	chr14:32217355-32217854	HepG2	liver:	n/a	n/a
14	ARID3A	chr14:32336820-32337151	HepG2	liver:	n/a	n/a
15	ARID3A	chr14:32406856-32407357	HepG2	liver:	n/a	n/a
16	ARID3A	chr14:32371298-32371463	K562	blood:	n/a	n/a
17	ARID3A	chr14:32186760-32187276	HepG2	liver:	n/a	n/a
18	ARID3A	chr14:32371343-32371443	HepG2	liver:	n/a	n/a
19	ARID3A	chr14:32545081-32545232	HepG2	liver:	n/a	n/a
20	ARID3A	chr14:32410542-32410944	HepG2	liver:	n/a	n/a
21	ARID3A	chr14:32435419-32435511	K562	blood:	n/a	n/a
22	ARID3A	chr14:32436746-32437119	HepG2	liver:	n/a	n/a
23	ARID3A	chr14:32551687-32552005	HepG2	liver:	n/a	n/a
24	ARID3A	chr14:32420002-32420133	K562	blood:	n/a	n/a
25	ARID3A	chr14:32363573-32363850	K562	blood:	n/a	n/a
26	ARID3A	chr14:32556802-32556966	HepG2	liver:	n/a	n/a
27	ARID3A	chr14:32256749-32256838	K562	blood:	n/a	n/a
28	ARID3A	chr14:32413392-32414034	HepG2	liver:	n/a	n/a
29	ARID3A	chr14:32550079-32550350	K562	blood:	n/a	n/a
30	ARID3A	chr14:32405430-32405611	HepG2	liver:	n/a	n/a
31	ARID3A	chr14:32555201-32555254	HepG2	liver:	n/a	n/a
32	ARID3A	chr14:32395314-32395700	HepG2	liver:	n/a	n/a
33	ARID3A	chr14:32479711-32480126	HepG2	liver:	n/a	n/a
34	ARID3A	chr14:32542760-32543259	HepG2	liver:	n/a	chr14:32543182-32543198
35	ARID3A	chr14:32328061-32328458	HepG2	liver:	n/a	n/a
36	ARID3A	chr14:32324410-32324953	HepG2	liver:	n/a	n/a
37	ATF1	chr14:32479764-32480124	K562	blood:	n/a	n/a
38	ATF1	chr14:32542827-32543050	K562	blood:	n/a	n/a
39	ATF1	chr14:32346315-32346347	K562	blood:	n/a	n/a
40	ATF1	chr14:32396643-32396811	K562	blood:	n/a	n/a
41	ATF1	chr14:32406911-32407288	K562	blood:	n/a	n/a
42	ATF1	chr14:32363503-32363948	K562	blood:	n/a	n/a
43	ATF1	chr14:32372421-32372751	K562	blood:	n/a	n/a
44	ATF1	chr14:32370963-32371540	K562	blood:	n/a	n/a
45	ATF2	chr14:32406895-32407392	GM12878	blood:	n/a	n/a
46	ATF3	chr14:32406922-32407305	K562	blood:	n/a	n/a
47	ATF3	chr14:32475366-32476465	A549	lung:	n/a	n/a
48	ATF3	chr14:32479691-32480286	A549	lung:	n/a	n/a
49	ATF3	chr14:32371180-32371540	K562	blood:	n/a	n/a
50	ATF3	chr14:32371304-32371469	K562	blood:	n/a	n/a

(count:1710 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:32328771-32328821	ProgFib	skin:	n/a
2	chr14:32181048-32181098	HPAEpiC	pulmonary alveolar:	n/a
3	chr14:32328771-32328821	ProgFib	skin:	n/a
4	chr14:32181048-32181098	HPAEpiC	pulmonary alveolar:	n/a
5	chr14:32545637-32545687	HEEpiC	esophagus:	n/a
6	chr14:32169802-32169852	RPTEC	kidney:	n/a
7	chr14:32547277-32547327	HMEC	breast:	n/a
8	chr14:32546633-32546683	HNPCEpiC	eye:	n/a
9	chr14:32170077-32170127	HRE	kidney:	n/a
10	chr14:32479397-32479447	HAEpiC	amniotic membrane:	n/a
11	chr14:32545637-32545687	RPTEC	kidney:	n/a
12	chr14:32545277-32545327	ECC-1	luminal epithelium:	n/a
13	chr14:32350324-32350374	HRPEpiC	eye:	n/a
14	chr14:32546939-32546989	HNPCEpiC	eye:	n/a
15	chr14:32545637-32545687	GM12891	blood:	n/a
16	chr14:32364560-32364610	AG04450	lung:	fetal
17	chr14:32546448-32546498	LNCaP	prostate:	n/a
18	chr14:32396820-32396870	K562	blood:	n/a
19	chr14:32169802-32169852	MCF-7	breast:	n/a
20	chr14:32546457-32546507	MCF-7	breast:	n/a
21	chr14:32543373-32543423	HUVEC	blood vessel:	n/a
22	chr14:32413698-32413748	HCF	heart:	n/a
23	chr14:32545008-32545058	HepG2	liver:	n/a
24	chr14:32420205-32420255	A549	lung:	n/a
25	chr14:32546448-32546498	CMK	blood:	n/a
26	chr14:32546939-32546989	MCF-7	breast:	n/a
27	chr14:32545277-32545327	SK-N-MC	brain:	n/a
28	chr14:32435490-32435540	NT2-D1	testis:	n/a
29	chr14:32546939-32546989	HRPEpiC	eye:	n/a
30	chr14:32364560-32364610	SAEC	small airway:	n/a
31	chr14:32364560-32364610	GM06990	blood:	n/a
32	chr14:32350428-32350478	HRCEpiC	kidney:	n/a
33	chr14:32546448-32546498	AG09309	skin:	n/a
34	chr14:32479397-32479447	SAEC	small airway:	n/a
35	chr14:32546466-32546516	U87	brain:	n/a
36	chr14:32328771-32328821	Hela-S3	cervix:	n/a
37	chr14:32350428-32350478	NHDF-neo	bronchial:	n/a
38	chr14:32396820-32396870	HPAEpiC	pulmonary alveolar:	n/a
39	chr14:32363503-32363553	MCF-7	breast:	n/a
40	chr14:32546466-32546516	BE2_C	brain:	n/a
41	chr14:32546466-32546516	AG09319	gingival:	n/a
42	chr14:32545637-32545687	AG09309	skin:	n/a
43	chr14:32547277-32547327	HEEpiC	esophagus:	n/a
44	chr14:32546448-32546498	HRPEpiC	eye:	n/a
45	chr14:32364560-32364610	HEK293	kidney:	embryo
46	chr14:32181048-32181098	GM12892	blood:	n/a
47	chr14:32545008-32545058	AG04449	skin:	fetal
48	chr14:32546448-32546498	GM19239	blood:	n/a
49	chr14:32475172-32475222	SK-N-SH	brain:	n/a
50	chr14:32364560-32364610	AG04449	skin:	fetal

(count:136 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr14:32195719..32197688-chr14:32198704..32200404,2	MCF-7	breast:
2	chr14:32552263..32554999-chr14:32566747..32569255,3	MCF-7	breast:
3	chr14:32486806..32489024-chr14:32506921..32508527,2	MCF-7	breast:
4	chr14:31979520..31980020-chr14:32542725..32543442,2	MCF-7	breast:
5	chr14:32388285..32389795-chr14:32392007..32393966,2	K562	blood:
6	chr14:32479672..32482357-chr14:32482780..32485449,2	K562	blood:
7	chr14:32123058..32124663-chr14:32126123..32128762,2	K562	blood:
8	chr14:32527861..32529646-chr14:32531253..32533373,2	K562	blood:
9	chr14:32394986..32395973-chr14:32938340..32938867,2	K562	blood:
10	chr14:32493473..32496779-chr14:32499147..32501066,3	MCF-7	breast:
11	chr14:32452982..32453943-chr14:32542808..32543419,2	MCF-7	breast:
12	chr14:32532795..32535626-chr14:32538600..32540501,3	MCF-7	breast:
13	chr14:32482420..32487455-chr14:32488055..32491731,6	K562	blood:
14	chr14:32542502..32543704-chr14:32720937..32721764,5	MCF-7	breast:
15	chr14:32404484..32405348-chr14:32542806..32543426,2	MCF-7	breast:
16	chr14:32555927..32560391-chr14:32562569..32565184,4	K562	blood:
17	chr14:31979147..31979905-chr14:32256388..32256891,2	MCF-7	breast:
18	chr14:32564995..32566566-chr14:32566776..32569180,2	MCF-7	breast:
19	chr14:32477098..32479521-chr14:32541403..32543078,2	MCF-7	breast:
20	chr14:32545781..32547471-chr14:32556657..32559505,2	K562	blood:
21	chr14:32479921..32481688-chr14:32482054..32483773,2	MCF-7	breast:
22	chr14:32412347..32415225-chr14:32417011..32419996,3	MCF-7	breast:
23	chr14:32510775..32512563-chr14:32517658..32519388,2	MCF-7	breast:
24	chr14:32482420..32486257-chr14:32487238..32491731,4	K562	blood:
25	chr14:32542534..32543435-chr14:32713337..32714270,5	MCF-7	breast:
26	chr14:32493473..32496779-chr14:32499147..32501066,3	MCF-7	breast:
27	chr14:32394037..32396201-chr16:75304956..75307730,2	MCF-7	breast:
28	chr14:32540232..32544144-chr14:32544366..32548398,5	MCF-7	breast:
29	chr14:32290973..32293409-chr14:32296887..32298672,2	K562	blood:
30	chr14:32534222..32536706-chr14:32540619..32542386,2	MCF-7	breast:
31	chr14:32385965..32386716-chr8:88512662..88513393,2	MCF-7	breast:
32	chr14:32477098..32479521-chr14:32541403..32543078,2	MCF-7	breast:
33	chr14:32303855..32305860-chr14:32313557..32315760,2	MCF-7	breast:
34	chr14:32341518..32343411-chr14:32344329..32346208,2	MCF-7	breast:
35	chr14:32250042..32252755-chr14:32254053..32255704,2	MCF-7	breast:
36	chr14:32316314..32318915-chr14:32319714..32322323,3	K562	blood:
37	chr14:32535687..32537246-chr14:32539696..32541400,2	K562	blood:
38	chr14:32404853..32406467-chr14:32545391..32547317,2	MCF-7	breast:
39	chr14:32409592..32411316-chr14:32413977..32416384,2	K562	blood:
40	chr14:32532497..32535433-chr14:32543249..32545498,2	MCF-7	breast:
41	chr14:32407172..32410124-chr14:32413888..32415450,2	MCF-7	breast:
42	chr14:32415369..32417109-chr14:32417144..32419896,2	MCF-7	breast:
43	chr14:32290973..32293409-chr14:32296388..32299179,4	K562	blood:
44	chr14:32564995..32566566-chr14:32566776..32569180,2	MCF-7	breast:
45	chr14:32303855..32305860-chr14:32313557..32315760,2	MCF-7	breast:
46	chr14:32545768..32548128-chr14:32672317..32675290,2	MCF-7	breast:
47	chr14:32544948..32548496-chr14:32669195..32673537,9	MCF-7	breast:
48	chr14:32295269..32297310-chr14:32302685..32304466,2	K562	blood:
49	chr14:32555927..32560391-chr14:32562569..32566454,5	K562	blood:
50	chr14:32476023..32478025-chr14:32478200..32480738,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C14orf126-4	chr14:32544625-32545905	NR_027263
2	lnc-C14orf126-4	chr14:32544625-32545999	ENSG00000258655.1
3	lnc-C14orf126-3	chr14:32398586-32399352	ENSG00000257472
4	lnc-C14orf126-3	chr14:32395007-32395475	ENSG00000257472
5	lnc-ARHGAP5-1	chr14:32545664-32545834	XLOC_010791
6	lnc-C14orf126-4	chr14:32545356-32546002	NONHSAT036299
7	lnc-ARHGAP5-1	chr14:32543521-32545423	XLOC_010791

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	NUBPL	hsa-miR-24-3p	chr14:32329735-32329757

Variant related genes	Relation type
ENSG00000258386	TF binding region
ARHGAP5-AS1	TF binding region
NUBPL	TF binding region
RNU6-602P	TF binding region
ENSG00000257472	TF binding region
ARHGAP5	TF binding region
ENSG00000258474	TF binding region
RNU6-455P	TF binding region
ENSG00000258386	CpG island
ARHGAP5-AS1	CpG island
NUBPL	CpG island
RNU6-602P	CpG island
ENSG00000257472	CpG island
ARHGAP5	CpG island
ENSG00000258474	CpG island
RNU6-455P	CpG island
ENSG00000201654	chromatin interactions
ENSG00000258655	chromatin interactions
ENSG00000202337	chromatin interactions
ENSG00000172270	chromatin interactions
ENSG00000100852	chromatin interactions
ENSG00000151413	chromatin interactions
ENSG00000258619	chromatin interactions
ENSG00000258474	chromatin interactions
ENSG00000258386	chromatin interactions

Extended variants
information (count: 17393 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:17393 , 50 per page) page: 1 2 3 4 5 6 7 ... 348

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564651727	chr14:32110547-32110548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs566627883	chr14:32110560-32110561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs531982176	chr14:32110588-32110589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs372169440	chr14:32110630-32110631	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs533771162	chr14:32110633-32110634	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs547345492	chr14:32110644-32110645	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs565583210	chr14:32110735-32110736	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs559955518	chr14:32110744-32110745	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs190447866	chr14:32110834-32110835	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs376345703	chr14:32110845-32110846	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs181633722	chr14:32110906-32110907	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs113842249	chr14:32110926-32110927	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs185185788	chr14:32110944-32110945	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs556668842	chr14:32110972-32110973	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs138566384	chr14:32111000-32111001	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs115932180	chr14:32111009-32111010	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374473513	chr14:32111024-32111025	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538790616	chr14:32111034-32111035	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs368373442	chr14:32111035-32111036	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs572396874	chr14:32111076-32111077	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs2120142	chr14:32111095-32111096	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs554850176	chr14:32111114-32111115	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs75052558	chr14:32111133-32111134	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200205124	chr14:32111176-32111177	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2120141	chr14:32111177-32111178	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs575265248	chr14:32111179-32111180	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs546463127	chr14:32111198-32111199	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs565363817	chr14:32111199-32111200	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs576864358	chr14:32111219-32111220	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189260372	chr14:32111220-32111221	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs540817252	chr14:32111272-32111273	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552282944	chr14:32111283-32111284	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs141773322	chr14:32111313-32111314	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs115837522	chr14:32111329-32111330	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548471035	chr14:32111334-32111335	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563597564	chr14:32111340-32111341	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530856754	chr14:32111385-32111386	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs563120198	chr14:32111401-32111402	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs570594390	chr14:32111405-32111406	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539118331	chr14:32111418-32111419	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs547578738	chr14:32111431-32111432	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs144522954	chr14:32111445-32111446	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181250299	chr14:32111450-32111451	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs74690303	chr14:32111471-32111472	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs370023719	chr14:32111472-32111473	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs537380796	chr14:32111486-32111487	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs34508949	chr14:32111495-32111496	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559106414	chr14:32111572-32111573	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs148062960	chr14:32111587-32111588	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2120140	chr14:32111622-32111623	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chronic myeloid leukemia	16756668	CNVD
Sudden cardiac death	19188705	CNVD
Pilocytic astrocytoma	18670637	CNVD
Multiple myeloma	16616336	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21045282	CNVD
Cancer	21129771	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21990379	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:4520 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:32046200-32110600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr14:32109800-32115400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:32110600-32112200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr14:32112200-32123200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr14:32114000-32116200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr14:32114200-32120400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr14:32115200-32115800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
8	chr14:32115400-32115600	ZNF genes & repeats	Pancreas	Pancrea
9	chr14:32115400-32115800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr14:32115600-32116800	Weak transcription	Pancreas	Pancrea
11	chr14:32116600-32117800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr14:32116600-32125000	Weak transcription	Fetal Kidney	kidney
13	chr14:32116800-32117000	ZNF genes & repeats	Pancreas	Pancrea
14	chr14:32117000-32148200	Weak transcription	Pancreas	Pancrea
15	chr14:32118400-32122800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr14:32119200-32122200	Weak transcription	Psoas Muscle	Psoas
17	chr14:32120400-32120600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr14:32121800-32130400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr14:32122000-32122800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr14:32122000-32123400	ZNF genes & repeats	Liver	Liver
21	chr14:32122600-32127800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr14:32123200-32123400	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr14:32123400-32123600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr14:32123400-32125400	Weak transcription	Fetal Heart	heart
25	chr14:32123400-32125800	Weak transcription	Liver	Liver
26	chr14:32123600-32129600	Weak transcription	Primary T cells from cord blood	blood
27	chr14:32123800-32126000	Weak transcription	Primary T cells fromperipheralblood	blood
28	chr14:32125600-32126000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr14:32127600-32128400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr14:32128200-32128800	Enhancers	Rectal Mucosa Donor 31	rectum
31	chr14:32129200-32130200	Enhancers	GM12878-XiMat	blood
32	chr14:32129600-32129800	Enhancers	Primary T cells from cord blood	blood
33	chr14:32131400-32131600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr14:32131600-32131800	Enhancers	Gastric	stomach
35	chr14:32131800-32132000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr14:32135200-32135400	Enhancers	HepG2	liver
37	chr14:32135200-32147000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr14:32135400-32147000	Weak transcription	HepG2	liver
39	chr14:32135800-32170800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr14:32136000-32144200	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr14:32136200-32147000	Weak transcription	Fetal Stomach	stomach
42	chr14:32136800-32137000	Weak transcription	Left Ventricle	heart
43	chr14:32137000-32137200	Enhancers	Left Ventricle	heart
44	chr14:32137000-32138200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr14:32137000-32146800	Weak transcription	Spleen	Spleen
46	chr14:32137200-32137400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr14:32137200-32138000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
48	chr14:32137200-32138200	ZNF genes & repeats	Fetal Intestine Small	intestine
49	chr14:32137200-32147000	Weak transcription	Skeletal Muscle Male	skeletal muscle
50	chr14:32137200-32147400	Weak transcription	Left Ventricle	heart

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