Variant report

Variant	nsv1005732
Chromosome Location	chr3:141917615-142090111
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2098)
CpG islands
(count:854)
Chromatin interactive
region (count:107)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:2098 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:142085451-142085580	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:142004029-142004406	K562	blood:	n/a	n/a
3	ARID3A	chr3:142082266-142082975	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:142034735-142035065	K562	blood:	n/a	n/a
5	ARID3A	chr3:142034796-142035079	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:141944333-141944542	K562	blood:	n/a	n/a
7	ARID3A	chr3:142085359-142085586	K562	blood:	n/a	n/a
8	ARID3A	chr3:141944275-141944587	HepG2	liver:	n/a	n/a
9	ARID3A	chr3:141941528-141942036	K562	blood:	n/a	n/a
10	ARID3A	chr3:142037995-142038366	K562	blood:	n/a	n/a
11	ATF1	chr3:142034743-142035113	K562	blood:	n/a	n/a
12	ATF1	chr3:141944202-141944637	K562	blood:	n/a	n/a
13	ATF1	chr3:142026474-142026530	K562	blood:	n/a	n/a
14	ATF1	chr3:141994868-141995043	K562	blood:	n/a	n/a
15	ATF1	chr3:142038012-142038223	K562	blood:	n/a	n/a
16	ATF1	chr3:142004039-142004362	K562	blood:	n/a	n/a
17	ATF2	chr3:141944124-141944603	GM12878	blood:	n/a	n/a
18	ATF2	chr3:141944313-141944572	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF3	chr3:142034698-142035057	K562	blood:	n/a	n/a
20	ATF3	chr3:141944306-141944624	K562	blood:	n/a	chr3:141944456-141944466
21	BACH1	chr3:142037995-142038332	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr3:141988570-141988640	K562	blood:	n/a	n/a
23	BACH1	chr3:141944121-141944594	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr3:142037969-142038499	K562	blood:	n/a	n/a
25	BATF	chr3:142074556-142074897	GM12878	blood:	n/a	n/a
26	BATF	chr3:141975772-141975937	GM12878	blood:	n/a	n/a
27	BCLAF1	chr3:141998774-141999206	GM12878	blood:	n/a	n/a
28	BCLAF1	chr3:141998835-141999218	GM12878	blood:	n/a	n/a
29	BCLAF1	chr3:141944193-141944635	GM12878	blood:	n/a	n/a
30	BHLHE40	chr3:141998833-141999090	HepG2	liver:	n/a	n/a
31	BHLHE40	chr3:141998901-141999171	GM12878	blood:	n/a	n/a
32	BHLHE40	chr3:141998848-141999153	K562	blood:	n/a	n/a
33	BHLHE40	chr3:141944084-141944604	HepG2	liver:	n/a	n/a
34	BHLHE40	chr3:141944144-141944582	GM12878	blood:	n/a	n/a
35	BHLHE40	chr3:142066400-142066735	K562	blood:	n/a	n/a
36	BHLHE40	chr3:141943947-141944618	K562	blood:	n/a	chr3:141944033-141944049
37	BRCA1	chr3:141944283-141944600	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr3:141933218-141933348	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr3:141994588-141995155	Hela-S3	cervix:	n/a	n/a
40	CBX3	chr3:141998618-141999310	K562	blood:	n/a	n/a
41	CBX3	chr3:141943716-141945024	K562	blood:	n/a	n/a
42	CBX3	chr3:142003802-142004433	K562	blood:	n/a	n/a
43	CBX3	chr3:141998807-141999224	K562	blood:	n/a	n/a
44	CBX3	chr3:142006799-142007385	HCT-116	colon:	n/a	n/a
45	CBX3	chr3:141972002-141972303	K562	blood:	n/a	n/a
46	CBX3	chr3:141974109-141974466	K562	blood:	n/a	n/a
47	CBX3	chr3:141951267-141951575	K562	blood:	n/a	n/a
48	CBX3	chr3:141972050-141972272	K562	blood:	n/a	n/a
49	CBX3	chr3:141951133-141951609	K562	blood:	n/a	n/a
50	CBX3	chr3:142003887-142004274	K562	blood:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:141944620-141944670	BE2_C	brain:	n/a
2	chr3:141944318-141944368	HAEpiC	amniotic membrane:	n/a
3	chr3:141944620-141944670	PANC-1	pancreas:	n/a
4	chr3:141944318-141944368	MCF-7	breast:	n/a
5	chr3:141944516-141944566	GM12892	blood:	n/a
6	chr3:141943895-141943945	HRE	kidney:	n/a
7	chr3:141945790-141945840	Caco-2	colon:	n/a
8	chr3:141945790-141945840	HMEC	breast:	n/a
9	chr3:141944344-141944394	PANC-1	pancreas:	n/a
10	chr3:142027066-142027116	A549	lung:	n/a
11	chr3:141943895-141943945	SK-N-SH	brain:	n/a
12	chr3:141945790-141945840	HEK293	kidney:	embryo
13	chr3:141944077-141944127	RPTEC	kidney:	n/a
14	chr3:142027066-142027116	HL-60	blood:	n/a
15	chr3:141944300-141944350	HAEpiC	amniotic membrane:	n/a
16	chr3:141928789-141928839	PANC-1	pancreas:	n/a
17	chr3:141944516-141944566	AoSMC	blood vessel:	n/a
18	chr3:141928789-141928839	AG09309	skin:	n/a
19	chr3:141945790-141945840	HAEpiC	amniotic membrane:	n/a
20	chr3:141944318-141944368	AG09319	gingival:	n/a
21	chr3:141944318-141944368	NHDF-neo	bronchial:	n/a
22	chr3:141945790-141945840	AoSMC	blood vessel:	n/a
23	chr3:141944620-141944670	HCT-116	colon:	n/a
24	chr3:141944516-141944566	NB4	blood:	n/a
25	chr3:141944519-141944569	HEK293	kidney:	embryo
26	chr3:141928789-141928839	RPTEC	kidney:	n/a
27	chr3:141944620-141944670	AoSMC	blood vessel:	n/a
28	chr3:141944519-141944569	RPTEC	kidney:	n/a
29	chr3:141944516-141944566	A549	lung:	n/a
30	chr3:141928789-141928839	GM12878	blood:	n/a
31	chr3:141945703-141945753	SK-N-SH_RA	brain:	n/a
32	chr3:141944300-141944350	SK-N-SH	brain:	n/a
33	chr3:141928789-141928839	HRCEpiC	kidney:	n/a
34	chr3:141944620-141944670	HAEpiC	amniotic membrane:	n/a
35	chr3:141944300-141944350	HIPEpiC	eye:	n/a
36	chr3:141944318-141944368	HPAEpiC	pulmonary alveolar:	n/a
37	chr3:141945703-141945753	PANC-1	pancreas:	n/a
38	chr3:141928789-141928839	MCF-7	breast:	n/a
39	chr3:141944620-141944670	AG09319	gingival:	n/a
40	chr3:141945790-141945840	HL-60	blood:	n/a
41	chr3:141944516-141944566	MCF-7	breast:	n/a
42	chr3:141945790-141945840	NT2-D1	testis:	n/a
43	chr3:141944300-141944350	GM06990	blood:	n/a
44	chr3:142027066-142027116	HNPCEpiC	eye:	n/a
45	chr3:141944620-141944670	PrEC	prostate:	n/a
46	chr3:141944344-141944394	SAEC	small airway:	n/a
47	chr3:141944300-141944350	GM12878	blood:	n/a
48	chr3:141944344-141944394	SK-N-SH	brain:	n/a
49	chr3:141995701-141995751	GM12878	blood:	n/a
50	chr3:141944620-141944670	HPAEpiC	pulmonary alveolar:	n/a

(count:107 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr3:141681127..141682067-chr3:141998956..141999598,2	MCF-7	breast:
2	chr3:141983516..141986399-chr3:141987635..141990028,2	MCF-7	breast:
3	chr3:141930773..141933744-chr3:141940549..141942064,2	MCF-7	breast:
4	chr3:141740842..141741377-chr3:141998535..141999516,2	K562	blood:
5	chr3:141929745..141931253-chr3:141941462..141943511,2	MCF-7	breast:
6	chr3:141943937..141944882-chr5:32585069..32586043,2	Hela-S3	cervix:
7	chr3:142066835..142068380-chr3:142068524..142070586,2	K562	blood:
8	chr1:149857842..149858808-chr3:141944067..141944956,2	Hela-S3	cervix:
9	chr3:142028519..142031113-chr3:142035238..142036947,2	K562	blood:
10	chr3:141831489..141833335-chr3:141922195..141926170,3	K562	blood:
11	chr3:141944534..141946087-chr3:141987477..141990045,2	MCF-7	breast:
12	chr3:141986894..141989145-chr3:141996424..141998046,2	K562	blood:
13	chr3:141944430..141944948-chr7:35839962..35840580,2	Hela-S3	cervix:
14	chr3:142025469..142027957-chr3:142037548..142040461,2	K562	blood:
15	chr3:141944534..141946087-chr3:141987477..141990045,2	MCF-7	breast:
16	chr3:141944032..141945017-chr8:143808717..143809376,2	Hela-S3	cervix:
17	chr3:142031696..142033287-chr3:142037661..142039925,2	MCF-7	breast:
18	chr3:141942954..141945885-chr3:141988032..141991755,3	MCF-7	breast:
19	chr3:141921447..141923041-chr3:141938532..141940338,2	K562	blood:
20	chr3:142077588..142080075-chr3:142081701..142083765,2	K562	blood:
21	chr3:141986894..141989145-chr3:141996424..141998046,2	K562	blood:
22	chr17:62222919..62223709-chr3:141944062..141944934,2	HCT-116	colon:
23	chr3:141918846..141920526-chr3:141922656..141925151,2	K562	blood:
24	chr3:141916087..141917951-chr3:141939342..141941586,2	K562	blood:
25	chr3:141933025..141940048-chr3:141942272..141945803,9	MCF-7	breast:
26	chr3:141927414..141929752-chr3:141932597..141934385,2	MCF-7	breast:
27	chr3:141899184..141899896-chr3:141998534..141999076,2	MCF-7	breast:
28	chr3:142026133..142029209-chr3:142034990..142037893,3	MCF-7	breast:
29	chr3:141943457..141944964-chr3:141968920..141970444,2	MCF-7	breast:
30	chr3:141844721..141845463-chr3:141945183..141945790,2	MCF-7	breast:
31	chr3:141919674..141922479-chr3:141924056..141926779,2	MCF-7	breast:
32	chr3:141929745..141931253-chr3:141941462..141943511,2	MCF-7	breast:
33	chr3:141924115..141926296-chr3:141927657..141929893,2	K562	blood:
34	chr3:141928249..141931424-chr3:141932973..141936618,4	K562	blood:
35	chr17:80184285..80186683-chr3:141942385..141945027,2	MCF-7	breast:
36	chr3:141983516..141986399-chr3:141987635..141990028,2	MCF-7	breast:
37	chr3:141919047..141920973-chr3:141943572..141945964,2	MCF-7	breast:
38	chr3:141844475..141845747-chr3:141998357..141999102,5	K562	blood:
39	chr3:142064702..142067188-chr3:142070699..142072268,2	K562	blood:
40	chr3:141745328..141748975-chr3:142003993..142005586,3	K562	blood:
41	chr3:142061779..142063304-chr3:142065930..142068810,2	K562	blood:
42	chr3:141919625..141921887-chr3:141933849..141936243,2	K562	blood:
43	chr3:141914914..141916949-chr3:141917367..141920269,2	K562	blood:
44	chr3:141930773..141933744-chr3:141940549..141942064,2	MCF-7	breast:
45	chr3:142042619..142044340-chr3:142047762..142050315,2	K562	blood:
46	chr3:141944137..141946098-chr3:141949464..141952210,3	K562	blood:
47	chr3:141939241..141942550-chr3:141942923..141945578,4	MCF-7	breast:
48	chr3:141844885..141845509-chr3:141998474..141999186,2	MCF-7	breast:
49	chr3:141918846..141920526-chr3:141922656..141925151,2	K562	blood:
50	chr3:141924115..141926296-chr3:141927657..141929893,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	XRN1	hsa-miR-10a-5p	chr3:142029586-142029608
2	XRN1	hsa-let-7b-5p	chr3:142030132-142030126
3	XRN1	hsa-miR-335-5p	chr3:142025482-142025506
4	XRN1	hsa-miR-10a-5p	chr3:142029592-142029585

Variant related genes	Relation type
GK5	TF binding region
XRN1	TF binding region
GK5	CpG island
XRN1	CpG island
ENSG00000228878	chromatin interactions
ENSG00000266402	chromatin interactions
ENSG00000113387	chromatin interactions
ENSG00000175054	chromatin interactions
ENSG00000160183	chromatin interactions
ENSG00000114127	chromatin interactions
ENSG00000122545	chromatin interactions
ENSG00000202444	chromatin interactions
ENSG00000175066	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000141526	chromatin interactions
ENSG00000114126	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000253806	chromatin interactions
ENSG00000272565	chromatin interactions
ENSG00000125968	chromatin interactions
ENSG00000130193	chromatin interactions
ENSG00000199753	chromatin interactions

Extended variants
information (count: 5321 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:5321 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547534539	chr3:141917619-141917620	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs372392881	chr3:141917625-141917626	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs549640855	chr3:141917632-141917633	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs74592286	chr3:141917718-141917719	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs375723171	chr3:141917722-141917723	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs74836705	chr3:141917810-141917811	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528871361	chr3:141917824-141917825	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs547477227	chr3:141917825-141917826	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs565591823	chr3:141917851-141917852	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs182493993	chr3:141917902-141917903	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs551722115	chr3:141917966-141917967	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs558980957	chr3:141918009-141918010	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs200622590	chr3:141918034-141918035	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs192681097	chr3:141918035-141918036	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs139220168	chr3:141918041-141918042	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574093857	chr3:141918044-141918045	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs143247187	chr3:141918052-141918053	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs184717143	chr3:141918063-141918064	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201733733	chr3:141918067-141918068	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529216433	chr3:141918071-141918072	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs80104894	chr3:141918083-141918084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs187367282	chr3:141918378-141918379	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs192550578	chr3:141918443-141918444	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs543350513	chr3:141918467-141918468	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs561607427	chr3:141918607-141918608	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs566429496	chr3:141918611-141918612	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs559695773	chr3:141918615-141918616	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs34465065	chr3:141918623-141918624	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs528884319	chr3:141918679-141918680	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs533213017	chr3:141918681-141918682	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs9841672	chr3:141918699-141918700	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs34765657	chr3:141918706-141918707	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs184793551	chr3:141918831-141918832	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs533668898	chr3:141918936-141918937	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs147533560	chr3:141918938-141918939	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs558125880	chr3:141918940-141918941	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs199626700	chr3:141918941-141918942	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs567578467	chr3:141918942-141918943	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs202073717	chr3:141918963-141918964	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs200598318	chr3:141918964-141918965	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs201569870	chr3:141918970-141918971	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs140239832	chr3:141918988-141918989	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs141125458	chr3:141919034-141919035	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs190297553	chr3:141919071-141919072	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs188683648	chr3:141919072-141919073	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs553129769	chr3:141919087-141919088	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs181026267	chr3:141919092-141919093	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs538801032	chr3:141919097-141919098	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs184308757	chr3:141919104-141919105	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs553433072	chr3:141919130-141919131	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
abnormal development	18461090	CNVD
Cancer	21129771	CNVD
Ovarian cancer	23621864	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:3419 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:141868800-141943000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr3:141869000-141922200	Weak transcription	A549	lung
3	chr3:141869000-141926800	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr3:141881000-141920800	Weak transcription	Small Intestine	intestine
5	chr3:141881600-141922800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr3:141883600-141927200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr3:141888000-141943200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr3:141888200-141922600	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr3:141888400-141922600	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr3:141888400-141927200	Weak transcription	GM12878-XiMat	blood
11	chr3:141888400-141930000	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr3:141888600-141928600	Weak transcription	Brain Hippocampus Middle	brain
13	chr3:141889000-141943600	Weak transcription	Psoas Muscle	Psoas
14	chr3:141889200-141920800	Weak transcription	Brain Cingulate Gyrus	brain
15	chr3:141889200-141920800	Weak transcription	Spleen	Spleen
16	chr3:141889200-141922400	Weak transcription	Fetal Brain Male	brain
17	chr3:141889400-141922600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr3:141889400-141922800	Weak transcription	NHLF	lung
19	chr3:141889400-141926600	Weak transcription	Primary B cells from peripheral blood	blood
20	chr3:141889400-141928200	Weak transcription	HSMMtube	muscle
21	chr3:141889400-141928400	Weak transcription	HUVEC	blood vessel
22	chr3:141889400-141928600	Weak transcription	Brain Substantia Nigra	brain
23	chr3:141889600-141926600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr3:141890000-141920800	Weak transcription	Gastric	stomach
25	chr3:141890000-141920800	Weak transcription	Thymus	Thymus
26	chr3:141890000-141921000	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr3:141890000-141922800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr3:141890000-141922800	Weak transcription	NHEK	skin
29	chr3:141890000-141929000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
30	chr3:141893800-141926600	Weak transcription	Primary T helper cells PMA-I stimulated	--
31	chr3:141896400-141926600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr3:141896600-141921200	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr3:141896600-141930000	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr3:141896600-141943200	Weak transcription	HMEC	breast
35	chr3:141898000-141922800	Weak transcription	NHDF-Ad	bronchial
36	chr3:141898800-141922600	Weak transcription	Hela-S3	cervix
37	chr3:141899200-141920000	Weak transcription	Placenta	Placenta
38	chr3:141899600-141920800	Weak transcription	Pancreas	Pancrea
39	chr3:141899800-141921000	Weak transcription	Colonic Mucosa	Colon
40	chr3:141900000-141920800	Weak transcription	Primary B cells from cord blood	blood
41	chr3:141900000-141920800	Weak transcription	Fetal Brain Female	brain
42	chr3:141900400-141920200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr3:141900400-141920800	Weak transcription	Rectal Smooth Muscle	rectum
44	chr3:141900400-141922400	Weak transcription	Brain Anterior Caudate	brain
45	chr3:141900600-141920800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr3:141900800-141920800	Weak transcription	Brain Germinal Matrix	brain
47	chr3:141901000-141921000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr3:141901400-141922800	Weak transcription	Primary T helper cells fromperipheralblood	blood
49	chr3:141902000-141929200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
50	chr3:141902200-141920000	Weak transcription	Skeletal Muscle Female	skeletal muscle

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