Variant report

Variant	nsv945920
Chromosome Location	chr1:46073152-46073884
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:28)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:28 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr1:46073418-46073669	H1-hESC	embryonic stem cell:	n/a	n/a
2	POLR2A	chr1:46073798-46073813	Gliobla	brain:	n/a	n/a
3	POLR2A	chr1:46073344-46074000	H1-hESC	embryonic stem cell:	n/a	n/a
4	POLR2A	chr1:46073420-46073455	MCF-7	breast:	n/a	n/a
5	POLR2A	chr1:46073764-46074512	GM12892	blood:	n/a	n/a
6	POLR2A	chr1:46072620-46076787	H1-hESC	embryonic stem cell:	n/a	n/a
7	POLR2A	chr1:46073584-46074118	Hela-S3	cervix:	n/a	n/a
8	POLR2A	chr1:46073332-46073803	K562	blood:	n/a	n/a
9	POLR2A	chr1:46073358-46073529	H1-hESC	embryonic stem cell:	n/a	n/a
10	POLR2A	chr1:46073206-46073730	SK-N-MC	brain:	n/a	n/a
11	POLR2A	chr1:46073190-46073664	GM12891	blood:	n/a	n/a
12	POLR2A	chr1:46073046-46074749	GM12878	blood:	n/a	n/a
13	POLR2A	chr1:46073216-46074546	GM12892	blood:	n/a	n/a
14	POLR2A	chr1:46073482-46073605	K562	blood:	n/a	n/a
15	POLR2A	chr1:46073847-46073952	GM12878	blood:	n/a	n/a
16	POLR2A	chr1:46072960-46074725	GM12892	blood:	n/a	n/a
17	POLR2A	chr1:46073349-46074591	H1-hESC	embryonic stem cell:	n/a	n/a
18	POLR2A	chr1:46071949-46077053	HepG2	liver:	n/a	n/a
19	POLR2A	chr1:46072597-46073878	K562	blood:	n/a	n/a
20	POLR2A	chr1:46073313-46073479	Hela-S3	cervix:	n/a	n/a
21	POLR2A	chr1:46073315-46073973	Hela-S3	cervix:	n/a	n/a
22	POLR2A	chr1:46072602-46074693	K562	blood:	n/a	n/a
23	POLR2A	chr1:46073819-46074599	GM12891	blood:	n/a	n/a
24	POLR2A	chr1:46073463-46073504	MCF-7	breast:	n/a	n/a
25	POLR2A	chr1:46073403-46073419	MCF-7	breast:	n/a	n/a
26	POLR2A	chr1:46072965-46074640	GM12878	blood:	n/a	n/a
27	POLR2A	chr1:46073334-46074064	GM12892	blood:	n/a	n/a
28	POLR2A	chr1:46073384-46073397	H1-hESC	embryonic stem cell:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:46073731-46073781	U87	brain:	n/a
2	chr1:46073731-46073781	Jurkat	blood:	n/a
3	chr1:46073731-46073781	HL-60	blood:	n/a
4	chr1:46073731-46073781	ECC-1	luminal epithelium:	n/a
5	chr1:46073731-46073781	GM12892	blood:	n/a
6	chr1:46073731-46073781	H1-hESC	embryonic stem cell:	embryo
7	chr1:46073731-46073781	A549	lung:	n/a
8	chr1:46073731-46073781	HEK293	kidney:	embryo
9	chr1:46073731-46073781	HPAEpiC	pulmonary alveolar:	n/a
10	chr1:46073731-46073781	AG09309	skin:	n/a
11	chr1:46073731-46073781	HCF	heart:	n/a
12	chr1:46073731-46073781	GM12891	blood:	n/a
13	chr1:46073731-46073781	HEEpiC	esophagus:	n/a
14	chr1:46073731-46073781	GM19239	blood:	n/a
15	chr1:46073731-46073781	HUVEC	blood vessel:	n/a
16	chr1:46073731-46073781	PANC-1	pancreas:	n/a
17	chr1:46073731-46073781	HCPEpiC	choroid plexus:	n/a
18	chr1:46073731-46073781	ovcar-3	ovarian:	n/a
19	chr1:46073731-46073781	K562	blood:	n/a
20	chr1:46073731-46073781	AG04450	lung:	fetal
21	chr1:46073731-46073781	Caco-2	colon:	n/a
22	chr1:46073731-46073781	GM06990	blood:	n/a
23	chr1:46073731-46073781	HepG2	liver:	n/a
24	chr1:46073731-46073781	LNCaP	prostate:	n/a
25	chr1:46073731-46073781	HRPEpiC	eye:	n/a
26	chr1:46073731-46073781	SK-N-SH	brain:	n/a
27	chr1:46073731-46073781	AG09319	gingival:	n/a
28	chr1:46073731-46073781	AoSMC	blood vessel:	n/a
29	chr1:46073731-46073781	BJ	skin:	n/a
30	chr1:46073731-46073781	HMEC	breast:	n/a
31	chr1:46073731-46073781	T-47D	breast:	n/a
32	chr1:46073731-46073781	SK-N-SH_RA	brain:	n/a
33	chr1:46073731-46073781	HNPCEpiC	eye:	n/a
34	chr1:46073731-46073781	NHBE	bronchial:	n/a
35	chr1:46073731-46073781	HRE	kidney:	n/a
36	chr1:46073731-46073781	PFSK-1	brain:	n/a
37	chr1:46073731-46073781	SK-N-MC	brain:	n/a
38	chr1:46073731-46073781	IMR90	lung:	fetal
39	chr1:46073731-46073781	HIPEpiC	eye:	n/a
40	chr1:46073731-46073781	NH-A	brain:	n/a
41	chr1:46073731-46073781	RPTEC	kidney:	n/a
42	chr1:46073731-46073781	AG10803	skin:	n/a
43	chr1:46073731-46073781	SAEC	small airway:	n/a
44	chr1:46073731-46073781	Hela-S3	cervix:	n/a
45	chr1:46073731-46073781	Hepatocyte	liver:	n/a
46	chr1:46073731-46073781	ProgFib	skin:	n/a
47	chr1:46073731-46073781	HCT-116	colon:	n/a
48	chr1:46073731-46073781	NHDF-neo	bronchial:	n/a
49	chr1:46073731-46073781	CMK	blood:	n/a
50	chr1:46073731-46073781	BE2_C	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:45986916..45989039-chr1:46073191..46077083,3	K562	blood:
2	chr1:46048568..46053199-chr1:46070794..46073826,5	K562	blood:

No data

Variant related genes	Relation type
NASP	TF binding region
NASP	CpG island
ENSG00000117450	chromatin interactions
ENSG00000132780	chromatin interactions

Extended variants
information (count: 54 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:54 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150700116	chr1:46073154-46073155	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs149829161	chr1:46073159-46073160	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs112075833	chr1:46073168-46073169	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs563076445	chr1:46073177-46073178	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs146543664	chr1:46073190-46073191	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs368955502	chr1:46073204-46073205	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs6698807	chr1:46073246-46073247	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs143172762	chr1:46073264-46073265	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs200423416	chr1:46073273-46073274	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs140271488	chr1:46073299-46073300	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs137972558	chr1:46073318-46073319	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs201683842	chr1:46073323-46073324	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs201684799	chr1:46073341-46073342	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs376920709	chr1:46073348-46073349	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs78094239	chr1:46073361-46073362	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs75187774	chr1:46073362-46073363	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs202027114	chr1:46073372-46073373	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs199792714	chr1:46073373-46073374	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs549617824	chr1:46073380-46073381	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs546772700	chr1:46073408-46073409	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs201219258	chr1:46073451-46073452	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs369112826	chr1:46073453-46073454	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs373754862	chr1:46073468-46073469	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs375520000	chr1:46073473-46073474	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs189352487	chr1:46073484-46073485	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs550837993	chr1:46073486-46073487	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs569085519	chr1:46073488-46073489	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs2230657	chr1:46073489-46073490	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs139726233	chr1:46073491-46073492	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs146584753	chr1:46073508-46073509	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs147691168	chr1:46073517-46073518	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs200027699	chr1:46073539-46073540	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs202213034	chr1:46073552-46073553	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs201446871	chr1:46073553-46073554	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs535215279	chr1:46073566-46073567	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs75124546	chr1:46073569-46073570	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs570742294	chr1:46073586-46073587	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs76379164	chr1:46073597-46073598	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs544511027	chr1:46073602-46073603	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs200936475	chr1:46073618-46073619	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs147021326	chr1:46073628-46073629	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs142198790	chr1:46073661-46073662	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs563173360	chr1:46073663-46073664	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs375742982	chr1:46073667-46073668	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs200497808	chr1:46073697-46073698	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs370255034	chr1:46073706-46073707	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs560873126	chr1:46073716-46073717	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs180902823	chr1:46073719-46073720	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs528141974	chr1:46073725-46073726	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs571767551	chr1:46073735-46073736	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	17603634	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Uveal melanoma	20484589	CNVD
Ovarian cancer	22174824	CNVD
Muscle-eye-brain disease	21572526	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	20680643	CNVD
Colorectal cancer	19287155	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Schizophrenia	20967226	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:157 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:46052000-46081000	Weak transcription	Small Intestine	intestine
2	chr1:46052200-46084200	Weak transcription	Right Atrium	heart
3	chr1:46052400-46080600	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr1:46052800-46078400	Weak transcription	Brain Cingulate Gyrus	brain
5	chr1:46052800-46081000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr1:46052800-46086000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:46052800-46089200	Strong transcription	HUES6 Cell Line	embryonic stem cell
8	chr1:46052800-46099400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr1:46053200-46127400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr1:46053600-46086000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
11	chr1:46055000-46085200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
12	chr1:46055200-46090400	Strong transcription	Dnd41	blood
13	chr1:46056000-46079000	Weak transcription	Colon Smooth Muscle	Colon
14	chr1:46056800-46073400	Weak transcription	Right Ventricle	heart
15	chr1:46056800-46074000	Weak transcription	Brain Substantia Nigra	brain
16	chr1:46057400-46081600	Weak transcription	Psoas Muscle	Psoas
17	chr1:46060800-46076200	Weak transcription	Esophagus	oesophagus
18	chr1:46061000-46073200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr1:46061000-46073200	Weak transcription	Pancreas	Pancrea
20	chr1:46061000-46073200	Weak transcription	Spleen	Spleen
21	chr1:46061000-46076200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr1:46061000-46078800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr1:46061400-46073200	Weak transcription	Brain Angular Gyrus	brain
24	chr1:46061400-46073200	Weak transcription	Lung	lung
25	chr1:46061600-46075200	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr1:46061600-46075200	Weak transcription	Colonic Mucosa	Colon
27	chr1:46062400-46074000	Weak transcription	Skeletal Muscle Male	skeletal muscle
28	chr1:46062600-46074200	Weak transcription	Brain Anterior Caudate	brain
29	chr1:46066400-46073200	Strong transcription	Primary T helper cells fromperipheralblood	blood
30	chr1:46066600-46075000	Weak transcription	Fetal Heart	heart
31	chr1:46066800-46084400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr1:46066800-46086800	Strong transcription	K562	blood
33	chr1:46067000-46086400	Strong transcription	H1 Cell Line	embryonic stem cell
34	chr1:46067200-46086600	Strong transcription	HUES64 Cell Line	embryonic stem cell
35	chr1:46067200-46087400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr1:46067400-46086600	Strong transcription	HUES48 Cell Line	embryonic stem cell
37	chr1:46067600-46077000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr1:46067600-46077600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr1:46067800-46076800	Strong transcription	Primary T cells fromperipheralblood	blood
40	chr1:46068000-46073200	Strong transcription	ES-I3 Cell Line	embryonic stem cell
41	chr1:46068000-46073200	Strong transcription	Primary T helper cells PMA-I stimulated	--
42	chr1:46068000-46076800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr1:46068000-46077000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr1:46068000-46078800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
45	chr1:46068000-46086600	Strong transcription	Placenta	Placenta
46	chr1:46068200-46073200	Strong transcription	Primary T cells from cord blood	blood
47	chr1:46068200-46073400	Strong transcription	Primary B cells from cord blood	blood
48	chr1:46068200-46076600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr1:46068200-46085000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr1:46068200-46086600	Strong transcription	Duodenum Mucosa	Duodenum

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