Variant report

Variant	nsv550273
Chromosome Location	chr10:27640971-27701737
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:27649547-27649808	K562	blood:	n/a	n/a
2	ARID3A	chr10:27672857-27673169	HepG2	liver:	n/a	n/a
3	ATF1	chr10:27649531-27649804	K562	blood:	n/a	n/a
4	BATF	chr10:27649564-27649764	GM12878	blood:	n/a	n/a
5	BATF	chr10:27643692-27643988	GM12878	blood:	n/a	n/a
6	BCL11A	chr10:27643658-27644039	GM12878	blood:	n/a	n/a
7	BCL11A	chr10:27643724-27643987	GM12878	blood:	n/a	n/a
8	BCL3	chr10:27672617-27673252	A549	lung:	n/a	n/a
9	BCLAF1	chr10:27643572-27643923	GM12878	blood:	n/a	n/a
10	BHLHE40	chr10:27649517-27649830	GM12878	blood:	n/a	n/a
11	BHLHE40	chr10:27672558-27673044	HepG2	liver:	n/a	n/a
12	BHLHE40	chr10:27646116-27646388	K562	blood:	n/a	chr10:27646219-27646232 chr10:27646221-27646230 chr10:27646222-27646231 chr10:27646221-27646230
13	BHLHE40	chr10:27649567-27649799	K562	blood:	n/a	n/a
14	BRCA1	chr10:27672817-27673127	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr10:27681602-27681815	K562	blood:	n/a	n/a
16	CBX3	chr10:27681617-27681837	K562	blood:	n/a	n/a
17	CCNT2	chr10:27649596-27649806	K562	blood:	n/a	n/a
18	CEBPB	chr10:27649533-27649818	A549	lung:	n/a	chr10:27649675-27649686
19	CEBPB	chr10:27677739-27678016	HepG2	liver:	n/a	chr10:27677849-27677860
20	CEBPB	chr10:27679600-27679898	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr10:27669848-27670363	HepG2	liver:	n/a	chr10:27669887-27669899
22	CEBPB	chr10:27672658-27673316	A549	lung:	n/a	n/a
23	CEBPB	chr10:27662837-27663055	K562	blood:	n/a	chr10:27662910-27662921
24	CEBPB	chr10:27649513-27649869	IMR90	lung:	n/a	chr10:27649675-27649686
25	CEBPB	chr10:27672755-27673183	A549	lung:	n/a	n/a
26	CEBPB	chr10:27649503-27649883	K562	blood:	n/a	chr10:27649675-27649686
27	CEBPB	chr10:27677693-27677915	MCF-7	breast:	n/a	chr10:27677849-27677860
28	CEBPB	chr10:27684721-27685002	Hela-S3	cervix:	n/a	chr10:27684883-27684896
29	CEBPB	chr10:27677736-27678037	IMR90	lung:	n/a	chr10:27677849-27677860
30	CEBPB	chr10:27659541-27659772	HepG2	liver:	n/a	chr10:27659628-27659639 chr10:27659627-27659638 chr10:27659627-27659640
31	CEBPB	chr10:27655050-27655300	K562	blood:	n/a	chr10:27655162-27655173 chr10:27655161-27655172 chr10:27655161-27655174
32	CEBPB	chr10:27672818-27673157	HepG2	liver:	n/a	n/a
33	CEBPB	chr10:27677675-27678050	Hela-S3	cervix:	n/a	chr10:27677849-27677860
34	CEBPB	chr10:27653947-27654086	K562	blood:	n/a	n/a
35	CEBPB	chr10:27662820-27663067	HepG2	liver:	n/a	chr10:27662910-27662921
36	CEBPB	chr10:27672728-27673265	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr10:27680208-27680388	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr10:27672803-27673162	MCF-7	breast:	n/a	n/a
39	CEBPB	chr10:27649575-27649846	HepG2	liver:	n/a	chr10:27649675-27649686
40	CEBPB	chr10:27655035-27655235	HepG2	liver:	n/a	chr10:27655162-27655173 chr10:27655161-27655172 chr10:27655161-27655174
41	CEBPB	chr10:27672754-27673203	A549	lung:	n/a	n/a
42	CHD1	chr10:27643797-27643865	GM12878	blood:	n/a	n/a
43	CHD2	chr10:27672857-27673148	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr10:27660335-27660679	K562	blood:	n/a	n/a
45	CTCF	chr10:27649541-27649855	A549	lung:	n/a	chr10:27649687-27649700 chr10:27649680-27649701 chr10:27649686-27649702 chr10:27649685-27649703
46	CTCF	chr10:27645167-27645372	HepG2	liver:	n/a	chr10:27645299-27645315 chr10:27645303-27645311 chr10:27645298-27645316 chr10:27645170-27645188 chr10:27645293-27645314
47	CTCF	chr10:27658876-27659061	HUVEC	blood vessel:	n/a	chr10:27658945-27658961 chr10:27658946-27658967 chr10:27658944-27658962
48	CTCF	chr10:27649531-27649892	MCF-7	breast:	n/a	chr10:27649687-27649700 chr10:27649680-27649701 chr10:27649686-27649702 chr10:27649685-27649703
49	CTCF	chr10:27644998-27645091	MCF-7	breast:	n/a	n/a
50	CTCF	chr10:27658915-27659027	GM12878	blood:	n/a	chr10:27658945-27658961 chr10:27658946-27658967 chr10:27658944-27658962

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:27698606-27698656	GM12891	blood:	n/a
2	chr10:27698606-27698656	NH-A	brain:	n/a
3	chr10:27698606-27698656	CMK	blood:	n/a
4	chr10:27698606-27698656	ProgFib	skin:	n/a
5	chr10:27698606-27698656	AG09309	skin:	n/a
6	chr10:27698606-27698656	GM12892	blood:	n/a
7	chr10:27698606-27698656	HEEpiC	esophagus:	n/a
8	chr10:27698606-27698656	SK-N-MC	brain:	n/a
9	chr10:27698606-27698656	SAEC	small airway:	n/a
10	chr10:27698606-27698656	HRPEpiC	eye:	n/a
11	chr10:27698606-27698656	HCPEpiC	choroid plexus:	n/a
12	chr10:27698606-27698656	NT2-D1	testis:	n/a
13	chr10:27698606-27698656	ovcar-3	ovarian:	n/a
14	chr10:27698606-27698656	K562	blood:	n/a
15	chr10:27698606-27698656	A549	lung:	n/a
16	chr10:27698606-27698656	PANC-1	pancreas:	n/a
17	chr10:27698606-27698656	LNCaP	prostate:	n/a
18	chr10:27698606-27698656	HIPEpiC	eye:	n/a
19	chr10:27698606-27698656	HNPCEpiC	eye:	n/a
20	chr10:27698606-27698656	SK-N-SH	brain:	n/a
21	chr10:27698606-27698656	SKMC	muscle:	n/a
22	chr10:27698606-27698656	BE2_C	brain:	n/a
23	chr10:27698606-27698656	HEK293	kidney:	embryo
24	chr10:27698606-27698656	HCT-116	colon:	n/a
25	chr10:27698606-27698656	Hepatocyte	liver:	n/a
26	chr10:27698606-27698656	HRE	kidney:	n/a
27	chr10:27698606-27698656	HCF	heart:	n/a
28	chr10:27698606-27698656	MCF-7	breast:	n/a
29	chr10:27698606-27698656	HepG2	liver:	n/a
30	chr10:27698606-27698656	BJ	skin:	n/a
31	chr10:27698606-27698656	U87	brain:	n/a
32	chr10:27698606-27698656	NB4	blood:	n/a
33	chr10:27698606-27698656	ECC-1	luminal epithelium:	n/a
34	chr10:27698606-27698656	HPAEpiC	pulmonary alveolar:	n/a
35	chr10:27698606-27698656	HL-60	blood:	n/a
36	chr10:27698606-27698656	HRCEpiC	kidney:	n/a
37	chr10:27698606-27698656	GM19239	blood:	n/a
38	chr10:27698606-27698656	Caco-2	colon:	n/a
39	chr10:27698606-27698656	MCF10A-Er-Src	breast:	n/a
40	chr10:27698606-27698656	HAEpiC	amniotic membrane:	n/a
41	chr10:27698606-27698656	RPTEC	kidney:	n/a
42	chr10:27698606-27698656	H1-hESC	embryonic stem cell:	embryo
43	chr10:27698606-27698656	PFSK-1	brain:	n/a
44	chr10:27698606-27698656	NHDF-neo	bronchial:	n/a
45	chr10:27698606-27698656	GM12878	blood:	n/a
46	chr10:27698606-27698656	IMR90	lung:	fetal
47	chr10:27698606-27698656	HUVEC	blood vessel:	n/a
48	chr10:27698606-27698656	AG10803	skin:	n/a
49	chr10:27698606-27698656	HMEC	breast:	n/a
50	chr10:27698606-27698656	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:27659175..27661663-chr10:27792060..27794224,2	MCF-7	breast:
2	chr10:27529763..27532096-chr10:27643724..27645777,2	MCF-7	breast:
3	chr10:27681780..27685010-chr10:27685683..27688279,3	K562	blood:
4	chr10:27530526..27532390-chr10:27644695..27646372,2	MCF-7	breast:
5	chr10:27669052..27671269-chr10:27683257..27685068,2	K562	blood:
6	chr10:27531028..27532588-chr10:27647976..27649755,2	K562	blood:
7	chr10:27659927..27662822-chr10:27662832..27664720,3	K562	blood:
8	chr10:27684512..27686768-chr10:27700849..27702736,2	K562	blood:
9	chr10:27669052..27671269-chr10:27683257..27685068,2	K562	blood:
10	chr10:27659927..27662822-chr10:27662832..27664720,3	K562	blood:
11	chr10:27694442..27697083-chr10:27703247..27705702,3	K562	blood:
12	chr10:27527860..27530153-chr10:27647076..27648802,2	MCF-7	breast:
13	chr10:27640371..27642415-chr10:27644846..27646556,2	K562	blood:
14	chr10:27640371..27642415-chr10:27644846..27646556,2	K562	blood:
15	chr10:27441984..27445191-chr10:27642152..27645235,3	MCF-7	breast:
16	chr10:27684512..27686768-chr10:27700849..27702736,2	K562	blood:
17	chr10:27681780..27685010-chr10:27685683..27688279,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTCHD3-1	chr10:27667067-27667291	NONHSAT011904

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PTCHD3	hsa-miR-128-3p	chr10:27687123-27687143

Variant related genes	Relation type
FAM210CP	TF binding region
TRIAP1P1	TF binding region
FAM210CP	CpG island
TRIAP1P1	CpG island
ENSG00000182077	chromatin interactions
ENSG00000107897	chromatin interactions
ENSG00000262412	chromatin interactions
ENSG00000136758	chromatin interactions
ENSG00000099246	chromatin interactions
ENSG00000120539	chromatin interactions

Extended variants
information (count: 1524 )
Associated
traits (count: 46 )

Variant overlapped rSNPs/rCNVs (count:1524 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1252786	chr10:27640971-27640972	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs1252787	chr10:27640978-27640979	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs146902598	chr10:27640983-27640984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs561616350	chr10:27640989-27640990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572074905	chr10:27640993-27640994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs367951853	chr10:27641001-27641002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs7902386	chr10:27641031-27641032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs545801692	chr10:27641055-27641056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs191719619	chr10:27641121-27641122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs115846402	chr10:27641181-27641182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552899407	chr10:27641198-27641199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs563124584	chr10:27641204-27641205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs531795645	chr10:27641265-27641266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs548729465	chr10:27641295-27641296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs568482063	chr10:27641306-27641307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs527739634	chr10:27641390-27641391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183570826	chr10:27641400-27641401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs56088980	chr10:27641415-27641416	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs188152275	chr10:27641455-27641456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191396825	chr10:27641473-27641474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182243555	chr10:27641505-27641506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs76847233	chr10:27641534-27641535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541277741	chr10:27641552-27641553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535309524	chr10:27641573-27641574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs555513441	chr10:27641585-27641586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs186477287	chr10:27641703-27641704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs78255369	chr10:27641751-27641752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs368422538	chr10:27641807-27641808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs192600857	chr10:27641812-27641813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs573546697	chr10:27641874-27641875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs7907633	chr10:27641933-27641934	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs143185702	chr10:27641941-27641942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs532003658	chr10:27641942-27641943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs542060893	chr10:27641944-27641945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs12414002	chr10:27641952-27641953	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs111999103	chr10:27641972-27641973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs547484694	chr10:27641995-27641996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs542390722	chr10:27642021-27642022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs570541079	chr10:27642028-27642029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs562580451	chr10:27642032-27642033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs184581896	chr10:27642079-27642080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs112985086	chr10:27642099-27642100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs569876291	chr10:27642112-27642113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs11015714	chr10:27642115-27642116	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs201044751	chr10:27642139-27642140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs555310813	chr10:27642147-27642148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs564736	chr10:27642166-27642167	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs149263466	chr10:27642181-27642182	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs11015715	chr10:27642191-27642192	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs557869527	chr10:27642206-27642207	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:46)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
Behavioral abnormalities	21522184	CNVD
Dysmorphic features	21522184	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Autism	21439084	CNVD
Maculopathy	20981449	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21525872	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:27633800-27655400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr10:27634600-27643200	Weak transcription	Right Atrium	heart
3	chr10:27635400-27641600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr10:27639000-27641600	Weak transcription	Fetal Muscle Leg	muscle
5	chr10:27639200-27643000	Weak transcription	Psoas Muscle	Psoas
6	chr10:27639200-27643000	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr10:27640200-27643000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr10:27641600-27643400	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr10:27641600-27644000	Enhancers	Fetal Muscle Leg	muscle
10	chr10:27642600-27644000	Enhancers	GM12878-XiMat	blood
11	chr10:27642800-27643200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr10:27642800-27643400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr10:27642800-27643400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr10:27642800-27643400	Enhancers	Brain Substantia Nigra	brain
15	chr10:27642800-27643600	Enhancers	Primary hematopoietic stem cells	blood
16	chr10:27642800-27643600	Enhancers	Fetal Heart	heart
17	chr10:27642800-27645400	Enhancers	Primary B cells from cord blood	blood
18	chr10:27642800-27645600	Enhancers	Primary B cells from peripheral blood	blood
19	chr10:27643000-27643200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr10:27643000-27643400	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr10:27643000-27643600	Enhancers	Sigmoid Colon	Sigmoid Colon
22	chr10:27643000-27643600	Active TSS	Monocytes-CD14+_RO01746	blood
23	chr10:27643000-27643800	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr10:27643000-27643800	Enhancers	Psoas Muscle	Psoas
25	chr10:27643000-27643800	Enhancers	Skeletal Muscle Female	skeletal muscle
26	chr10:27643200-27643400	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr10:27643200-27643400	Enhancers	Pancreas	Pancrea
28	chr10:27643200-27643600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr10:27643200-27643600	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr10:27643200-27643800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr10:27643200-27643800	Enhancers	Right Atrium	heart
32	chr10:27643200-27644000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
33	chr10:27643400-27643600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr10:27643400-27643600	Flanking Active TSS	Brain Hippocampus Middle	brain
35	chr10:27643400-27643600	Flanking Active TSS	Brain Substantia Nigra	brain
36	chr10:27643400-27643800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
37	chr10:27643400-27643800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
38	chr10:27643400-27643800	Enhancers	Primary T helper cells PMA-I stimulated	--
39	chr10:27643400-27643800	Enhancers	Primary T helper cells fromperipheralblood	blood
40	chr10:27643400-27643800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr10:27643400-27643800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr10:27643400-27643800	Enhancers	Osteobl	bone
43	chr10:27643400-27644000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr10:27643400-27644000	Active TSS	Rectal Mucosa Donor 29	rectum
45	chr10:27643400-27644000	Active TSS	Rectal Smooth Muscle	rectum
46	chr10:27643400-27645000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr10:27643400-27645800	Weak transcription	Pancreas	Pancrea
48	chr10:27643600-27643800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
49	chr10:27643600-27644000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr10:27643600-27644000	Enhancers	Primary T cells fromperipheralblood	blood

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