Variant report

Variant	nsv899006
Chromosome Location	chr12:38535661-38851642
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2343)
CpG islands
(count:2386)
Chromatin interactive
region (count:29)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2343 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:38543626-38543997	K562	blood:	n/a	n/a
2	ARID3A	chr12:38710113-38710696	HepG2	liver:	n/a	chr12:38710204-38710220 chr12:38710205-38710221
3	ARID3A	chr12:38722213-38722403	K562	blood:	n/a	n/a
4	ARID3A	chr12:38778647-38778789	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:38710301-38710555	K562	blood:	n/a	n/a
6	ARID3A	chr12:38722185-38722490	HepG2	liver:	n/a	n/a
7	ATF1	chr12:38580930-38581004	K562	blood:	n/a	n/a
8	ATF1	chr12:38562455-38562511	K562	blood:	n/a	n/a
9	ATF1	chr12:38592349-38592545	K562	blood:	n/a	n/a
10	ATF1	chr12:38710296-38710661	K562	blood:	n/a	n/a
11	ATF2	chr12:38744225-38745089	GM12878	blood:	n/a	n/a
12	ATF2	chr12:38744101-38745067	GM12878	blood:	n/a	n/a
13	ATF2	chr12:38710293-38710713	GM12878	blood:	n/a	n/a
14	ATF2	chr12:38710159-38710775	GM12878	blood:	n/a	n/a
15	ATF3	chr12:38710223-38710780	A549	lung:	n/a	n/a
16	ATF3	chr12:38710219-38710780	A549	lung:	n/a	n/a
17	BACH1	chr12:38543625-38544007	K562	blood:	n/a	n/a
18	BACH1	chr12:38778825-38779049	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr12:38722036-38722207	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr12:38541011-38541384	K562	blood:	n/a	n/a
21	BACH1	chr12:38535652-38536024	K562	blood:	n/a	n/a
22	BACH1	chr12:38536600-38536974	K562	blood:	n/a	n/a
23	BATF	chr12:38780253-38780450	GM12878	blood:	n/a	chr12:38780343-38780354
24	BATF	chr12:38786453-38786734	GM12878	blood:	n/a	chr12:38786626-38786637
25	BATF	chr12:38710371-38710641	GM12878	blood:	n/a	n/a
26	BATF	chr12:38744451-38744982	GM12878	blood:	n/a	n/a
27	BATF	chr12:38710378-38710679	GM12878	blood:	n/a	n/a
28	BATF	chr12:38744388-38744934	GM12878	blood:	n/a	n/a
29	BCL11A	chr12:38744355-38744996	GM12878	blood:	n/a	n/a
30	BCL11A	chr12:38744417-38744818	GM12878	blood:	n/a	n/a
31	BCL11A	chr12:38710258-38710721	GM12878	blood:	n/a	n/a
32	BCL3	chr12:38744447-38744862	GM12878	blood:	n/a	n/a
33	BCL3	chr12:38710141-38710775	A549	lung:	n/a	n/a
34	BCL3	chr12:38710209-38710812	A549	lung:	n/a	n/a
35	BCLAF1	chr12:38710098-38710795	GM12878	blood:	n/a	n/a
36	BCLAF1	chr12:38710352-38710785	K562	blood:	n/a	n/a
37	BCLAF1	chr12:38744312-38744895	GM12878	blood:	n/a	n/a
38	BCLAF1	chr12:38710117-38710847	GM12878	blood:	n/a	n/a
39	BHLHE40	chr12:38536598-38536976	K562	blood:	n/a	n/a
40	BHLHE40	chr12:38722157-38722342	GM12878	blood:	n/a	n/a
41	BHLHE40	chr12:38543621-38544008	K562	blood:	n/a	n/a
42	BHLHE40	chr12:38710409-38710609	K562	blood:	n/a	n/a
43	BHLHE40	chr12:38535395-38536023	K562	blood:	n/a	n/a
44	BHLHE40	chr12:38536603-38536976	GM12878	blood:	n/a	n/a
45	BHLHE40	chr12:38710353-38710663	HepG2	liver:	n/a	n/a
46	BHLHE40	chr12:38710156-38710702	GM12878	blood:	n/a	n/a
47	BHLHE40	chr12:38541011-38541378	K562	blood:	n/a	n/a
48	BRCA1	chr12:38535822-38535855	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr12:38543624-38544009	GM12878	blood:	n/a	n/a
50	BRCA1	chr12:38710358-38710669	GM12878	blood:	n/a	n/a

(count:2386 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:38546326-38546376	NT2-D1	testis:	n/a
2	chr12:38547997-38548047	NH-A	brain:	n/a
3	chr12:38710491-38710541	HL-60	blood:	n/a
4	chr12:38806793-38806843	HAEpiC	amniotic membrane:	n/a
5	chr12:38545085-38545135	K562	blood:	n/a
6	chr12:38710424-38710474	HEEpiC	esophagus:	n/a
7	chr12:38547997-38548047	GM06990	blood:	n/a
8	chr12:38546326-38546376	NT2-D1	testis:	n/a
9	chr12:38547997-38548047	NH-A	brain:	n/a
10	chr12:38710491-38710541	HL-60	blood:	n/a
11	chr12:38806793-38806843	HAEpiC	amniotic membrane:	n/a
12	chr12:38545085-38545135	K562	blood:	n/a
13	chr12:38710424-38710474	HEEpiC	esophagus:	n/a
14	chr12:38547997-38548047	GM06990	blood:	n/a
15	chr12:38550112-38550162	AG09319	gingival:	n/a
16	chr12:38724551-38724601	NH-A	brain:	n/a
17	chr12:38557136-38557186	BJ	skin:	n/a
18	chr12:38710491-38710541	Hela-S3	cervix:	n/a
19	chr12:38552636-38552686	PANC-1	pancreas:	n/a
20	chr12:38557136-38557186	A549	lung:	n/a
21	chr12:38547997-38548047	A549	lung:	n/a
22	chr12:38724551-38724601	GM12891	blood:	n/a
23	chr12:38710433-38710483	A549	lung:	n/a
24	chr12:38557350-38557400	PrEC	prostate:	n/a
25	chr12:38555758-38555808	PFSK-1	brain:	n/a
26	chr12:38554220-38554270	Jurkat	blood:	n/a
27	chr12:38553846-38553896	AG04449	skin:	fetal
28	chr12:38545214-38545264	NHDF-neo	bronchial:	n/a
29	chr12:38548782-38548832	HL-60	blood:	n/a
30	chr12:38548782-38548832	HUVEC	blood vessel:	n/a
31	chr12:38560974-38561024	HNPCEpiC	eye:	n/a
32	chr12:38557350-38557400	U87	brain:	n/a
33	chr12:38710154-38710204	LNCaP	prostate:	n/a
34	chr12:38710700-38710750	HUVEC	blood vessel:	n/a
35	chr12:38544936-38544986	AG10803	skin:	n/a
36	chr12:38710953-38711003	HEEpiC	esophagus:	n/a
37	chr12:38710700-38710750	HCPEpiC	choroid plexus:	n/a
38	chr12:38555758-38555808	HPAEpiC	pulmonary alveolar:	n/a
39	chr12:38554220-38554270	HPAEpiC	pulmonary alveolar:	n/a
40	chr12:38714149-38714199	H1-hESC	embryonic stem cell:	embryo
41	chr12:38557136-38557186	NB4	blood:	n/a
42	chr12:38556969-38557019	U87	brain:	n/a
43	chr12:38535710-38535760	GM12892	blood:	n/a
44	chr12:38560974-38561024	Hepatocyte	liver:	n/a
45	chr12:38595404-38595454	BE2_C	brain:	n/a
46	chr12:38553846-38553896	PFSK-1	brain:	n/a
47	chr12:38595404-38595454	IMR90	lung:	fetal
48	chr12:38710154-38710204	HPAEpiC	pulmonary alveolar:	n/a
49	chr12:38710953-38711003	HPAEpiC	pulmonary alveolar:	n/a
50	chr12:38548782-38548832	U87	brain:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:38843134..38845389-chr12:38847279..38849955,2	MCF-7	breast:
2	chr12:38721798..38722714-chr12:39305427..39306254,2	MCF-7	breast:
3	chr12:38722084..38722866-chr12:39667246..39667987,2	MCF-7	breast:
4	chr12:38764399..38764899-chr18:71815043..71815544,2	Hela-S3	cervix:
5	chr1:156184890..156186421-chr12:38543820..38545329,2	MCF-7	breast:
6	chr12:38637847..38640659-chr12:38643822..38646474,2	K562	blood:
7	chr12:38542325..38545309-chr16:33964713..33967583,2	K562	blood:
8	chr12:38543803..38545320-chr21:9824316..9826615,2	K562	blood:
9	chr12:38837698..38839402-chr12:38841166..38843830,2	K562	blood:
10	chr1:156185761..156186730-chr12:38543308..38544330,7	MCF-7	breast:
11	chr12:38536776..38537298-chr14:88237597..88238190,6	MCF-7	breast:
12	chr12:38536304..38537296-chr14:88237622..88238153,2	K562	blood:
13	chr12:38778961..38781578-chr12:38784417..38786236,2	MCF-7	breast:
14	chr12:38843134..38845389-chr12:38847279..38849955,2	MCF-7	breast:
15	chr12:38543320..38543832-chr21:9825931..9826770,2	K562	blood:
16	chr12:38542306..38543824-chr20:26188496..26191492,2	K562	blood:
17	chr12:38778961..38781578-chr12:38784417..38786236,2	MCF-7	breast:
18	chr12:38637847..38640659-chr12:38643822..38646474,2	K562	blood:
19	chr12:38535401..38535902-chr2:133016817..133017415,2	MCF-7	breast:
20	chr12:38721916..38722780-chr12:39497511..39498068,2	MCF-7	breast:
21	chr12:38845594..38847956-chr12:38851662..38853438,2	K562	blood:
22	chr12:38676913..38678502-chr12:38709612..38711993,2	MCF-7	breast:
23	chr1:156185820..156186795-chr12:38543314..38544329,6	MCF-7	breast:
24	chr12:38542302..38543806-chr20:26188737..26191492,2	K562	blood:
25	chr1:156185732..156186437-chr12:38543803..38544322,4	MCF-7	breast:
26	chr1:156184764..156186317-chr12:38543820..38545325,2	K562	blood:
27	chr1:156185862..156186566-chr12:38543820..38544329,3	MCF-7	breast:
28	chr12:38837698..38839402-chr12:38841166..38843830,2	K562	blood:
29	chr12:34175001..34175865-chr12:38710413..38711151,3	HCT-116	colon:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALG10B-3	chr12:38847317-38847776	NONHSAT027683
2	lnc-CPNE8-5	chr12:38824250-38824373	l_629_chr12:38821325-38838592_lung
3	lnc-ALG10B-3	chr12:38847317-38847681	NONHSAT027682
4	lnc-CPNE8-5	chr12:38821326-38822703	l_629_chr12:38821325-38838592_lung
5	lnc-CPNE8-5	chr12:38837923-38838124	l_629_chr12:38821325-38838592_lung
6	lnc-CPNE8-5	chr12:38832098-38832212	l_629_chr12:38821325-38838592_lung
7	lnc-CPNE8-6	chr12:38599188-38599814	NONHSAT027678
8	lnc-ALG10B-3	chr12:38846321-38846419	NONHSAT027683
9	lnc-ALG10B-3	chr12:38836308-38836412	NONHSAT027682
10	lnc-CPNE8-5	chr12:38838505-38838592	l_629_chr12:38821325-38838592_lung

No data

Variant related genes	Relation type
RNA5SP359	TF binding region
TUBB8P5	TF binding region
ALG10B	TF binding region
ENSG00000253016	TF binding region
ENSG00000257292	TF binding region
ENSG00000266333	TF binding region
ENSG00000258360	TF binding region
RNA5SP358	TF binding region
RNA5SP359	CpG island
TUBB8P5	CpG island
ALG10B	CpG island
ENSG00000253016	CpG island
ENSG00000257292	CpG island
ENSG00000266333	CpG island
ENSG00000258360	CpG island
RNA5SP358	CpG island
ENSG00000200434	chromatin interactions
ENSG00000227195	chromatin interactions
ENSG00000139133	chromatin interactions
ENSG00000264063	chromatin interactions
ENSG00000175548	chromatin interactions
ENSG00000141665	chromatin interactions
ENSG00000264462	chromatin interactions

Extended variants
information (count: 10857 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:10857 , 50 per page) page: 1 2 3 4 5 6 7 ... 218

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9652051	chr12:38535661-38535662	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs562708743	chr12:38535702-38535703	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs142526712	chr12:38535711-38535712	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs551546361	chr12:38535727-38535728	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs571499227	chr12:38535741-38535742	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs527562124	chr12:38535753-38535754	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs2387599	chr12:38535761-38535762	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs527715479	chr12:38535764-38535765	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs552702933	chr12:38535768-38535769	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs566888261	chr12:38535775-38535776	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145976358	chr12:38535777-38535778	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs11182447	chr12:38535803-38535804	ZNF genes & repeats Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs76120497	chr12:38535816-38535817	ZNF genes & repeats Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs569442940	chr12:38535824-38535825	ZNF genes & repeats Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs73271932	chr12:38535839-38535840	ZNF genes & repeats Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs113951953	chr12:38535848-38535849	ZNF genes & repeats Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs111898302	chr12:38535849-38535850	ZNF genes & repeats Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs78637695	chr12:38535850-38535851	ZNF genes & repeats Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs377187344	chr12:38535857-38535858	ZNF genes & repeats Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs117821761	chr12:38535864-38535865	ZNF genes & repeats Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs139843893	chr12:38535867-38535868	ZNF genes & repeats Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs1716913	chr12:38535875-38535876	ZNF genes & repeats Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs534477430	chr12:38535882-38535883	ZNF genes & repeats Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs191527254	chr12:38535893-38535894	ZNF genes & repeats Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs115675889	chr12:38535915-38535916	ZNF genes & repeats Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs149689823	chr12:38535920-38535921	ZNF genes & repeats Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs373008165	chr12:38535925-38535926	ZNF genes & repeats Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs112326051	chr12:38535927-38535928	ZNF genes & repeats Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs562885134	chr12:38535938-38535939	ZNF genes & repeats Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs144466719	chr12:38535953-38535954	ZNF genes & repeats Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs75633520	chr12:38535967-38535968	ZNF genes & repeats Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs564612256	chr12:38535971-38535972	ZNF genes & repeats Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs73106811	chr12:38535972-38535973	ZNF genes & repeats Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs182460793	chr12:38536012-38536013	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565076991	chr12:38536019-38536020	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527598529	chr12:38536074-38536075	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs112074991	chr12:38536096-38536097	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187079436	chr12:38536144-38536145	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs115677956	chr12:38536146-38536147	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531844140	chr12:38536153-38536154	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529602091	chr12:38536161-38536162	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549740399	chr12:38536186-38536187	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs189862516	chr12:38536188-38536189	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113193032	chr12:38536204-38536205	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538702303	chr12:38536213-38536214	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs148396834	chr12:38536215-38536216	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs11182448	chr12:38536227-38536228	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs151316413	chr12:38536233-38536234	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs554467126	chr12:38536249-38536250	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs116185559	chr12:38536255-38536256	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Autism	20858243	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:811 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:38533000-38536600	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr12:38533000-38536600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr12:38533000-38536600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr12:38533000-38536600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr12:38533000-38536600	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr12:38533000-38536600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr12:38533000-38536600	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr12:38533000-38536600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr12:38533000-38536600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr12:38533000-38536600	Weak transcription	Brain Cingulate Gyrus	brain
11	chr12:38533000-38536600	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr12:38533000-38536600	Weak transcription	Brain Substantia Nigra	brain
13	chr12:38533000-38536600	Weak transcription	Colon Smooth Muscle	Colon
14	chr12:38533000-38536600	Weak transcription	Esophagus	oesophagus
15	chr12:38533000-38536600	Weak transcription	Pancreas	Pancrea
16	chr12:38533000-38536600	Weak transcription	Stomach Mucosa	stomach
17	chr12:38533000-38536800	Weak transcription	Right Atrium	heart
18	chr12:38533200-38538200	Weak transcription	A549	lung
19	chr12:38534200-38557600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
20	chr12:38535200-38537000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
21	chr12:38535200-38537000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
22	chr12:38535200-38537000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
23	chr12:38535200-38537200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
24	chr12:38535400-38537000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr12:38535400-38537200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
26	chr12:38535600-38536000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr12:38535600-38537000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr12:38535600-38537000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr12:38535600-38537000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr12:38535600-38537200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
31	chr12:38535800-38536000	Bivalent Enhancer	Gastric	stomach
32	chr12:38535800-38536600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr12:38536400-38536600	Weak transcription	Fetal Lung	lung
34	chr12:38536400-38536600	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr12:38536400-38537000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr12:38536400-38537000	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr12:38536600-38536800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
38	chr12:38536600-38536800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr12:38536600-38536800	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
40	chr12:38536600-38536800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
41	chr12:38536600-38536800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr12:38536600-38536800	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
43	chr12:38536600-38536800	Bivalent Enhancer	Psoas Muscle	Psoas
44	chr12:38536600-38536800	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 29	rectum
45	chr12:38536600-38536800	Bivalent Enhancer	Rectal Smooth Muscle	rectum
46	chr12:38536600-38536800	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
47	chr12:38536600-38536800	Weak transcription	Thymus	Thymus
48	chr12:38536600-38537000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
49	chr12:38536600-38537000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
50	chr12:38536600-38537000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell

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