Variant report

Variant	esv3319335
Chromosome Location	chr1:85085389-85087937
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:32)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:85087934..85091159-chr1:85092418..85095457,3	K562	blood:
2	chr1:85038472..85040331-chr1:85083677..85087781,3	K562	blood:
3	chr1:85085152..85088621-chr1:85102581..85105385,3	K562	blood:
4	chr1:84606589..84609383-chr1:85086485..85089260,2	MCF-7	breast:
5	chr1:85078939..85082218-chr1:85082659..85086975,4	K562	blood:
6	chr1:85086321..85086904-chr1:85219114..85220306,4	K562	blood:
7	chr1:84907591..84908130-chr1:85086306..85086828,2	MCF-7	breast:
8	chr1:85087799..85089777-chr1:85107656..85110506,2	K562	blood:
9	chr1:85086229..85086777-chr1:85190143..85190708,2	K562	blood:
10	chr1:85039840..85040593-chr1:85086207..85086997,2	MCF-7	breast:
11	chr1:85083999..85086788-chr1:85190313..85192578,2	K562	blood:
12	chr1:85085136..85087140-chr1:85087403..85088994,2	K562	blood:
13	chr1:85038631..85041223-chr1:85086686..85088297,2	K562	blood:
14	chr1:85086362..85086938-chr6:26157676..26158194,2	NB4	blood:
15	chr1:85087266..85090257-chr1:85091189..85093358,2	K562	blood:
16	chr1:85083903..85087925-chr1:85089048..85091034,3	K562	blood:
17	chr1:85084850..85087042-chr1:85091218..85093725,2	K562	blood:
18	chr1:84907633..84908606-chr1:85086107..85087004,6	MCF-7	breast:
19	chr1:84959786..84961700-chr1:85087773..85090482,2	K562	blood:
20	chr1:85039597..85040122-chr1:85085833..85086565,2	NB4	blood:
21	chr1:85086553..85087333-chr1:85218935..85219853,3	MCF-7	breast:
22	chr1:85038036..85041091-chr1:85083677..85086665,3	K562	blood:
23	chr1:84999607..85002399-chr1:85083617..85085507,3	K562	blood:
24	chr1:85085136..85087140-chr1:85087403..85088994,2	K562	blood:
25	chr1:84961886..84966476-chr1:85082859..85087991,5	K562	blood:
26	chr1:84970609..84972253-chr1:85083424..85086384,2	K562	blood:
27	chr1:85039864..85042098-chr1:85083830..85086770,2	MCF-7	breast:
28	chr1:84969683..84973064-chr1:85084003..85088136,5	K562	blood:
29	chr1:85086327..85087159-chr1:85237711..85238512,3	K562	blood:
30	chr1:85083746..85086523-chr1:85204168..85206276,2	K562	blood:
31	chr1:85085152..85087256-chr1:85103081..85105385,2	K562	blood:
32	chr1:85084850..85087265-chr1:85092225..85094800,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C1orf180-1	chr1:85086440-85086497	XLOC_000895
2	lnc-C1orf180-1	chr1:85086440-85086469	NONHSAT004220

No data

Variant related genes	Relation type
ENSG00000174021	chromatin interactions
ENSG00000122432	chromatin interactions
ENSG00000232622	chromatin interactions
ENSG00000117151	chromatin interactions
KIAA0368	miRNA target sites

Extended variants
information (count: 105 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:105 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75033832	chr1:85085400-85085401	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs186819781	chr1:85085417-85085418	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs74095485	chr1:85085443-85085444	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs559722074	chr1:85085444-85085445	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs532245349	chr1:85085518-85085519	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs552068207	chr1:85085572-85085573	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs369289287	chr1:85085589-85085590	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs10640663	chr1:85085600-85085601	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs35442510	chr1:85085601-85085602	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs72508944	chr1:85085602-85085603	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs397786103	chr1:85085603-85085604	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs200415242	chr1:85085604-85085605	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs568940899	chr1:85085631-85085632	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs565475356	chr1:85085679-85085680	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs192399787	chr1:85085682-85085683	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs527866299	chr1:85085710-85085711	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs146695652	chr1:85085715-85085716	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs374941258	chr1:85085720-85085721	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs139062740	chr1:85085734-85085735	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs185637769	chr1:85085778-85085779	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs188572357	chr1:85085791-85085792	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs61186300	chr1:85085874-85085875	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs370865026	chr1:85085877-85085878	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs374465961	chr1:85085913-85085914	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs368552288	chr1:85085917-85085918	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs72491570	chr1:85085918-85085919	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs539327092	chr1:85085963-85085964	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs143995862	chr1:85085979-85085980	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs112619323	chr1:85086025-85086026	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs575747875	chr1:85086029-85086030	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs544831798	chr1:85086146-85086147	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs200538964	chr1:85086154-85086155	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs561334027	chr1:85086166-85086167	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs552203636	chr1:85086212-85086213	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs376645908	chr1:85086214-85086215	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs576272652	chr1:85086236-85086237	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs202042428	chr1:85086243-85086244	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs880412	chr1:85086250-85086251	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs145397655	chr1:85086260-85086261	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs192970819	chr1:85086289-85086290	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs552031027	chr1:85086300-85086301	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs562846400	chr1:85086322-85086323	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs531395265	chr1:85086345-85086346	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs548322656	chr1:85086387-85086388	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs569705469	chr1:85086399-85086400	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs568162438	chr1:85086423-85086424	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs2994434	chr1:85086434-85086435	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	mRNA abundance
48	rs35950527	chr1:85086477-85086478	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
49	rs12067196	chr1:85086494-85086495	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
50	rs2945136	chr1:85086520-85086521	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	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
Papillary thyroid carcinoma	21436994	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
Breast cancer	17603634	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
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	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
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	16397240	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:379 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:85077200-85085400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr1:85080200-85086000	Weak transcription	Pancreas	Pancrea
3	chr1:85080200-85086200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr1:85080400-85085600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr1:85080800-85086200	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr1:85082400-85086000	Enhancers	Rectal Smooth Muscle	rectum
7	chr1:85082800-85086200	Enhancers	Stomach Smooth Muscle	stomach
8	chr1:85084200-85085600	Enhancers	Colon Smooth Muscle	Colon
9	chr1:85084400-85085600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr1:85084400-85086200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr1:85084600-85086200	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr1:85084800-85085400	Enhancers	Ovary	ovary
13	chr1:85084800-85086200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr1:85084800-85086200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr1:85085000-85085400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr1:85085000-85085400	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr1:85085000-85085400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr1:85085000-85085400	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr1:85085000-85085400	Weak transcription	Left Ventricle	heart
20	chr1:85085000-85085400	Enhancers	NHEK	skin
21	chr1:85085000-85085600	Enhancers	Fetal Kidney	kidney
22	chr1:85085000-85085800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr1:85085000-85085800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr1:85085000-85085800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr1:85085000-85085800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
26	chr1:85085000-85085800	Flanking Active TSS	Brain Anterior Caudate	brain
27	chr1:85085000-85085800	Enhancers	Fetal Heart	heart
28	chr1:85085000-85085800	Flanking Active TSS	HUVEC	blood vessel
29	chr1:85085000-85086000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr1:85085000-85086000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr1:85085000-85086000	Enhancers	HSMMtube	muscle
32	chr1:85085000-85086200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr1:85085000-85086200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr1:85085000-85086200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
35	chr1:85085000-85086200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr1:85085000-85086200	Enhancers	Adipose Nuclei	Adipose
37	chr1:85085000-85086200	Enhancers	Duodenum Smooth Muscle	Duodenum
38	chr1:85085000-85086200	Enhancers	Fetal Intestine Large	intestine
39	chr1:85085000-85086200	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr1:85085200-85085400	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr1:85085200-85085400	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr1:85085200-85085400	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr1:85085200-85085400	Enhancers	Brain Angular Gyrus	brain
44	chr1:85085200-85085400	Flanking Active TSS	Brain Hippocampus Middle	brain
45	chr1:85085200-85085400	Enhancers	Rectal Mucosa Donor 29	rectum
46	chr1:85085200-85085400	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr1:85085200-85085600	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr1:85085200-85085600	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
49	chr1:85085200-85085800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr1:85085200-85085800	Bivalent Enhancer	HepG2	liver

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