Variant report

Variant	nsv967232
Chromosome Location	chr3:135871526-135887926
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:76)
CpG islands
(count:0)
Chromatin interactive
region (count:31)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:76 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr3:135873508-135873669	K562	blood:	n/a	n/a
2	BRCA1	chr3:135876601-135876657	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr3:135887829-135887948	K562	blood:	n/a	chr3:135887886-135887899
4	CEBPB	chr3:135880289-135880673	K562	blood:	n/a	chr3:135880457-135880468
5	CEBPB	chr3:135881317-135881526	K562	blood:	n/a	chr3:135881372-135881383
6	CEBPB	chr3:135880305-135880652	HepG2	liver:	n/a	chr3:135880457-135880468
7	CEBPB	chr3:135882236-135882532	MCF-7	breast:	n/a	n/a
8	CEBPB	chr3:135881280-135881522	H1-hESC	embryonic stem cell:	n/a	chr3:135881372-135881383
9	CEBPB	chr3:135877391-135877660	K562	blood:	n/a	n/a
10	CEBPB	chr3:135881200-135881525	MCF-7	breast:	n/a	chr3:135881372-135881383
11	CEBPB	chr3:135881259-135881480	HepG2	liver:	n/a	chr3:135881372-135881383
12	CEBPB	chr3:135877464-135877680	HepG2	liver:	n/a	n/a
13	CEBPB	chr3:135881343-135881507	A549	lung:	n/a	chr3:135881372-135881383
14	CEBPB	chr3:135880360-135880590	H1-hESC	embryonic stem cell:	n/a	chr3:135880457-135880468
15	CEBPB	chr3:135880295-135880646	IMR90	lung:	n/a	chr3:135880457-135880468
16	CEBPB	chr3:135880290-135880682	Hela-S3	cervix:	n/a	chr3:135880457-135880468
17	CEBPB	chr3:135882275-135882480	A549	lung:	n/a	n/a
18	CEBPB	chr3:135881242-135881519	Hela-S3	cervix:	n/a	chr3:135881372-135881383
19	CEBPB	chr3:135880335-135880637	A549	lung:	n/a	chr3:135880457-135880468
20	CEBPB	chr3:135882223-135882541	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr3:135874270-135874306	GM10266	blood:	n/a	n/a
22	CTCF	chr3:135885087-135885146	GM20000	blood:	n/a	n/a
23	CUX1	chr3:135887695-135887799	K562	blood:	n/a	n/a
24	E2F4	chr3:135877680-135877834	MCF10A-Er-Src	breast:	n/a	n/a
25	ESR1	chr3:135884955-135885168	ECC-1	luminal epithelium:	n/a	n/a
26	FOS	chr3:135871387-135871638	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr3:135880444-135880547	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr3:135880385-135880585	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr3:135871329-135871597	MCF10A-Er-Src	breast:	n/a	n/a
30	FOXA1	chr3:135885311-135885697	T-47D	breast:	n/a	chr3:135885541-135885553
31	FOXA1	chr3:135885382-135885641	T-47D	breast:	n/a	chr3:135885541-135885553
32	MAFK	chr3:135877719-135877975	HepG2	liver:	n/a	n/a
33	MAX	chr3:135882600-135882767	NB4	blood:	n/a	n/a
34	MYC	chr3:135882732-135882878	NB4	blood:	n/a	n/a
35	MYC	chr3:135886227-135886565	MCF10A-Er-Src	breast:	n/a	chr3:135886428-135886437
36	MYC	chr3:135871396-135871638	MCF10A-Er-Src	breast:	n/a	n/a
37	MYC	chr3:135871329-135871597	MCF10A-Er-Src	breast:	n/a	n/a
38	POLR2A	chr3:135883669-135883725	MCF-7	breast:	n/a	n/a
39	POLR2A	chr3:135887142-135887520	GM12878	blood:	n/a	n/a
40	POLR2A	chr3:135874503-135874585	MCF-7	breast:	n/a	n/a
41	POLR2A	chr3:135872466-135872472	HepG2	liver:	n/a	n/a
42	POLR2A	chr3:135881342-135881418	ProgFib	skin:	n/a	n/a
43	POLR2A	chr3:135876235-135876402	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr3:135879384-135879506	MCF-7	breast:	n/a	n/a
45	POLR2A	chr3:135877190-135877982	K562	blood:	n/a	n/a
46	POLR2A	chr3:135887481-135887487	MCF-7	breast:	n/a	n/a
47	POLR2A	chr3:135882637-135882643	MCF-7	breast:	n/a	n/a
48	POLR2A	chr3:135880244-135880523	HepG2	liver:	n/a	n/a
49	POLR2A	chr3:135875108-135875120	MCF10A-Er-Src	breast:	n/a	n/a
50	POLR2A	chr3:135881305-135881440	MCF-7	breast:	n/a	n/a

No data

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:135885984..135890346-chr3:135913669..135917315,5	MCF-7	breast:
2	chr3:135883267..135885538-chr3:135968468..135971038,3	K562	blood:
3	chr3:135865547..135867656-chr3:135871463..135873226,2	K562	blood:
4	chr3:135879587..135883583-chr3:135913683..135917123,7	MCF-7	breast:
5	chr3:135870250..135872855-chr3:135914710..135917326,2	K562	blood:
6	chr3:135886125..135888413-chr3:135893720..135896006,2	MCF-7	breast:
7	chr3:135876657..135878200-chr3:135910756..135912522,2	K562	blood:
8	chr3:135876607..135878545-chr3:135883402..135885999,2	K562	blood:
9	chr3:135874998..135877491-chr3:135913896..135916002,2	MCF-7	breast:
10	chr3:135874306..135876384-chr3:135885061..135886909,2	MCF-7	breast:
11	chr3:135883267..135884888-chr3:135968468..135971038,2	K562	blood:
12	chr3:135871018..135872662-chr3:135874899..135876560,2	MCF-7	breast:
13	chr3:135885575..135887195-chr3:135890153..135893026,2	MCF-7	breast:
14	chr3:135886209..135888091-chr3:135890757..135893050,2	K562	blood:
15	chr3:135884006..135886547-chr3:135914260..135916079,2	K562	blood:
16	chr3:135884038..135885594-chr3:135912255..135915096,2	MCF-7	breast:
17	chr3:135881427..135883402-chr3:135892260..135894929,2	MCF-7	breast:
18	chr3:135873199..135876113-chr3:135913654..135915671,2	K562	blood:
19	chr3:135883996..135885511-chr3:135967463..135969334,2	MCF-7	breast:
20	chr3:135861871..135864342-chr3:135869780..135872731,2	K562	blood:
21	chr3:135886156..135888628-chr3:135897104..135900045,2	MCF-7	breast:
22	chr3:135876607..135878545-chr3:135883402..135885999,2	K562	blood:
23	chr3:135867388..135869019-chr3:135870114..135872076,2	K562	blood:
24	chr3:135887141..135889698-chr3:135896091..135898192,2	K562	blood:
25	chr3:135861871..135867047-chr3:135867816..135873226,7	K562	blood:
26	chr3:135871355..135873070-chr3:135914710..135916565,2	K562	blood:
27	chr3:135870333..135872175-chr3:135909037..135911378,2	MCF-7	breast:
28	chr3:135885870..135888428-chr3:135911475..135915140,3	MCF-7	breast:
29	chr3:135881085..135883253-chr3:135914338..135916372,2	MCF-7	breast:
30	chr3:135866754..135872495-chr3:135912205..135917619,11	MCF-7	breast:
31	chr3:135871018..135872662-chr3:135874899..135876560,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPP2R3A-1	chr3:135874391-135874838	NONHSAT092274

No data

Variant related genes	Relation type
TDGF1P6	TF binding region
ENSG00000114054	chromatin interactions
ENSG00000241438	chromatin interactions
ENSG00000174579	chromatin interactions

Extended variants
information (count: 712 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:712 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149929074	chr3:135871560-135871561	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs533000067	chr3:135871585-135871586	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs374566316	chr3:135871592-135871593	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs201684396	chr3:135871601-135871602	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs201142509	chr3:135871609-135871610	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs528925835	chr3:135871610-135871611	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs548715971	chr3:135871620-135871621	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs199724419	chr3:135871622-135871623	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs367847791	chr3:135871628-135871629	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs372333467	chr3:135871645-135871646	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs111872749	chr3:135871674-135871675	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs552094684	chr3:135871676-135871677	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs534399804	chr3:135871682-135871683	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs571930421	chr3:135871708-135871709	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs373259101	chr3:135871714-135871715	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs534396410	chr3:135871719-135871720	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs556790764	chr3:135871750-135871751	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs554381086	chr3:135871753-135871754	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs567778128	chr3:135871769-135871770	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs552993001	chr3:135871797-135871798	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs556360184	chr3:135871803-135871804	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs576429819	chr3:135871813-135871814	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs545063858	chr3:135871833-135871834	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs188841777	chr3:135871853-135871854	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs557636973	chr3:135871953-135871954	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs539055622	chr3:135871999-135872000	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs192883915	chr3:135872044-135872045	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs377328348	chr3:135872087-135872088	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs183296404	chr3:135872130-135872131	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs559878373	chr3:135872144-135872145	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs529059150	chr3:135872149-135872150	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs34822700	chr3:135872174-135872175	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs370597671	chr3:135872184-135872185	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs542756497	chr3:135872201-135872202	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs552969653	chr3:135872213-135872214	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs7613398	chr3:135872229-135872230	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs551349198	chr3:135872275-135872276	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs572831480	chr3:135872341-135872342	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs571389084	chr3:135872351-135872352	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs374551474	chr3:135872361-135872362	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs144337842	chr3:135872367-135872368	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs571991932	chr3:135872411-135872412	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs186983668	chr3:135872422-135872423	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs527956889	chr3:135872440-135872441	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs60803776	chr3:135872463-135872464	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs548095043	chr3:135872483-135872484	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs538468588	chr3:135872489-135872490	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs559512639	chr3:135872540-135872541	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs567885980	chr3:135872556-135872557	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs191504152	chr3:135872583-135872584	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:53)

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
Cancer	21129771	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
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	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
Intracranial aneurysm	16715129	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
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18511947	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:619 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:135831400-135874800	Weak transcription	Fetal Brain Male	brain
2	chr3:135843800-135873800	Weak transcription	Colonic Mucosa	Colon
3	chr3:135845600-135880400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr3:135861600-135873000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr3:135861800-135872200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr3:135861800-135873000	Weak transcription	Stomach Mucosa	stomach
7	chr3:135862000-135904800	Weak transcription	Hela-S3	cervix
8	chr3:135862600-135872200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr3:135862600-135872200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr3:135864200-135872200	Strong transcription	HUES64 Cell Line	embryonic stem cell
11	chr3:135864200-135882400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr3:135864400-135882600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr3:135864400-135885200	Weak transcription	Brain Germinal Matrix	brain
14	chr3:135865200-135871800	Strong transcription	Fetal Thymus	thymus
15	chr3:135865600-135882400	Weak transcription	Fetal Heart	heart
16	chr3:135865800-135872200	Strong transcription	Dnd41	blood
17	chr3:135866000-135872000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr3:135866200-135872000	Strong transcription	Monocytes-CD14+_RO01746	blood
19	chr3:135866400-135871800	Strong transcription	Primary monocytes fromperipheralblood	blood
20	chr3:135866800-135872000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr3:135867400-135872200	Genic enhancers	Primary T helper cells fromperipheralblood	blood
22	chr3:135867400-135872400	Genic enhancers	Primary T helper cells PMA-I stimulated	--
23	chr3:135867800-135872000	Strong transcription	HUES48 Cell Line	embryonic stem cell
24	chr3:135867800-135872000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
25	chr3:135868000-135871600	Strong transcription	HepG2	liver
26	chr3:135868000-135872000	Strong transcription	Primary B cells from cord blood	blood
27	chr3:135868200-135871600	Strong transcription	Primary hematopoietic stem cells	blood
28	chr3:135868400-135871600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr3:135868400-135871800	Strong transcription	Primary B cells from peripheral blood	blood
30	chr3:135868400-135871800	Strong transcription	Placenta	Placenta
31	chr3:135868400-135872800	Strong transcription	Thymus	Thymus
32	chr3:135868600-135872000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
33	chr3:135868800-135883000	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr3:135869000-135871800	Strong transcription	HSMM	muscle
35	chr3:135869000-135872000	Strong transcription	Primary T cells from cord blood	blood
36	chr3:135869000-135876400	Weak transcription	HSMMtube	muscle
37	chr3:135869400-135871800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr3:135869400-135872000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
39	chr3:135869600-135871600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr3:135869600-135871600	Strong transcription	Duodenum Mucosa	Duodenum
41	chr3:135869600-135871600	Strong transcription	K562	blood
42	chr3:135869600-135872000	Genic enhancers	Primary T killer naive cells fromperipheralblood	blood
43	chr3:135869600-135872000	Strong transcription	Rectal Mucosa Donor 29	rectum
44	chr3:135869800-135871600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr3:135869800-135871600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr3:135869800-135871600	Strong transcription	Adipose Nuclei	Adipose
47	chr3:135869800-135871600	Genic enhancers	Brain Anterior Caudate	brain
48	chr3:135869800-135871600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr3:135869800-135871600	Strong transcription	Fetal Muscle Leg	muscle
50	chr3:135869800-135871600	Strong transcription	Stomach Smooth Muscle	stomach

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