Variant report

Variant	nsv525445
Chromosome Location	chr1:209885318-209912593
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:148)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:148 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:209901218-209901705	K562	blood:	n/a	n/a
2	ATF1	chr1:209901245-209901423	K562	blood:	n/a	n/a
3	ATF2	chr1:209897398-209897976	GM12878	blood:	n/a	n/a
4	ATF2	chr1:209897289-209897894	GM12878	blood:	n/a	n/a
5	BATF	chr1:209897334-209897783	GM12878	blood:	n/a	chr1:209897567-209897578
6	BATF	chr1:209900883-209901057	GM12878	blood:	n/a	n/a
7	BATF	chr1:209897311-209897669	GM12878	blood:	n/a	chr1:209897567-209897578
8	BATF	chr1:209907067-209907465	GM12878	blood:	n/a	chr1:209907298-209907309
9	BCL11A	chr1:209897328-209897763	GM12878	blood:	n/a	n/a
10	BCL3	chr1:209897327-209897792	GM12878	blood:	n/a	n/a
11	CEBPB	chr1:209906827-209907085	Hela-S3	cervix:	n/a	chr1:209906900-209906911
12	CEBPB	chr1:209906759-209907275	K562	blood:	n/a	chr1:209906900-209906911
13	CEBPB	chr1:209906794-209907193	IMR90	lung:	n/a	chr1:209906900-209906911
14	CEBPB	chr1:209906744-209907217	A549	lung:	n/a	chr1:209906900-209906911
15	CEBPB	chr1:209906840-209907055	H1-hESC	embryonic stem cell:	n/a	chr1:209906900-209906911
16	CEBPB	chr1:209906759-209907251	HepG2	liver:	n/a	chr1:209906900-209906911
17	CREB1	chr1:209897371-209897884	GM12878	blood:	n/a	n/a
18	CREB1	chr1:209894589-209894997	GM12878	blood:	n/a	n/a
19	CTCF	chr1:209898751-209898763	GM10266	blood:	n/a	n/a
20	CTCF	chr1:209898660-209898810	GM12878	blood:	n/a	n/a
21	CTCF	chr1:209898700-209898850	RPTEC	kidney:	n/a	n/a
22	CTCF	chr1:209898560-209898710	A549	lung:	n/a	n/a
23	CTCF	chr1:209898780-209898930	NHEK	skin:	n/a	n/a
24	CTCF	chr1:209898720-209898870	Caco-2	colon:	n/a	n/a
25	CTCF	chr1:209898680-209898830	HEEpiC	esophagus:	n/a	n/a
26	CTCF	chr1:209898560-209898710	HEEpiC	esophagus:	n/a	n/a
27	CTCF	chr1:209898740-209898890	RPTEC	kidney:	n/a	n/a
28	CTCF	chr1:209908640-209908790	Caco-2	colon:	n/a	n/a
29	CTCF	chr1:209898722-209898822	MCF-7	breast:	n/a	n/a
30	CTCF	chr1:209898715-209898793	LNCaP	prostate:	n/a	n/a
31	CTCF	chr1:209898920-209899070	SAEC	small airway:	n/a	n/a
32	CTCF	chr1:209898980-209899130	HEEpiC	esophagus:	n/a	n/a
33	CTCF	chr1:209898740-209898890	A549	lung:	n/a	n/a
34	CTCF	chr1:209898761-209898831	Kidney_OC	kidney:	n/a	n/a
35	CTCF	chr1:209898680-209898830	SAEC	small airway:	n/a	n/a
36	CTCF	chr1:209900971-209901141	K562	blood:	n/a	n/a
37	CTCF	chr1:209898720-209898870	HMEC	breast:	n/a	n/a
38	CTCF	chr1:209898652-209898922	K562	blood:	n/a	n/a
39	CTCF	chr1:209899060-209899210	GM12872	blood:	n/a	n/a
40	CTCF	chr1:209906880-209907030	HMF	breast:	n/a	n/a
41	CTCF	chr1:209898720-209898870	MCF-7	breast:	n/a	n/a
42	CTCF	chr1:209898640-209898790	HMEC	breast:	n/a	n/a
43	CTCF	chr1:209898700-209898850	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr1:209908920-209909070	GM12873	blood:	n/a	n/a
45	CTCF	chr1:209898580-209898730	NHEK	skin:	n/a	n/a
46	E2F4	chr1:209890392-209890592	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr1:209885792-209885992	MCF10A-Er-Src	breast:	n/a	n/a
48	EBF1	chr1:209897315-209897707	GM12878	blood:	n/a	n/a
49	EBF1	chr1:209907225-209907480	GM12878	blood:	n/a	n/a
50	EBF1	chr1:209907120-209907569	GM12878	blood:	n/a	n/a

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:209901763..209904735-chr1:209904804..209907749,3	K562	blood:
2	chr1:209887863..209889453-chr1:209910765..209912630,2	K562	blood:
3	chr1:209898728..209900231-chr1:209914075..209916050,2	K562	blood:
4	chr1:209900061..209902674-chr1:209907942..209909580,2	K562	blood:
5	chr1:209893922..209895818-chr1:210001055..210002815,2	MCF-7	breast:
6	chr1:209897489..209898995-chr1:209918699..209920810,2	K562	blood:
7	chr1:209898273..209898882-chr1:209921133..209921700,3	MCF-7	breast:
8	chr1:209877047..209878564-chr1:209885238..209887392,2	K562	blood:
9	chr1:209900061..209902674-chr1:209907942..209909580,2	K562	blood:
10	chr1:209887863..209889453-chr1:209910765..209912630,2	K562	blood:
11	chr1:209901763..209904735-chr1:209904804..209907749,3	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-G0S2-3	chr1:209894009-209894141	NONHSAT009229
2	lnc-G0S2-3	chr1:209894009-209894546	NONHSAT009228
3	lnc-LAMB3-1	chr1:209897375-209897470	ENSG00000227591.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	HSD11B1	hsa-miR-26b-5p	chr1:209908208-209908228

Variant related genes	Relation type
ENSG00000227591	TF binding region
ENSG00000117597	chromatin interactions
ENSG00000117594	chromatin interactions

Extended variants
information (count: 950 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:950 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11119328	chr1:209885318-209885319	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs556194670	chr1:209885329-209885330	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs968033	chr1:209885371-209885372	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs571637808	chr1:209885383-209885384	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs541862085	chr1:209885406-209885407	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs560274010	chr1:209885407-209885408	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs139502242	chr1:209885451-209885452	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs4844488	chr1:209885509-209885510	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs76824909	chr1:209885525-209885526	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs368458458	chr1:209885564-209885565	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs547338217	chr1:209885615-209885616	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs201539416	chr1:209885687-209885688	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs544045565	chr1:209885717-209885718	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs189321200	chr1:209885760-209885761	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs567627530	chr1:209885805-209885806	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs181979458	chr1:209885834-209885835	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs186525003	chr1:209885866-209885867	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs533298796	chr1:209885907-209885908	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs552079077	chr1:209885916-209885917	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs142810166	chr1:209885993-209885994	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs537648498	chr1:209886001-209886002	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs556360908	chr1:209886002-209886003	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs76879183	chr1:209886080-209886081	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs568398897	chr1:209886103-209886104	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs570258580	chr1:209886104-209886105	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs535417729	chr1:209886133-209886134	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs538842751	chr1:209886141-209886142	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs553848527	chr1:209886170-209886171	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs576940082	chr1:209886211-209886212	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs189391568	chr1:209886223-209886224	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs181033200	chr1:209886224-209886225	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs186525967	chr1:209886227-209886228	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs34148285	chr1:209886260-209886261	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs139729262	chr1:209886271-209886272	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs71636125	chr1:209886278-209886279	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs540237713	chr1:209886285-209886286	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs529573503	chr1:209886306-209886307	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs191226517	chr1:209886309-209886310	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs553764506	chr1:209886319-209886320	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs371428704	chr1:209886342-209886343	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs182768247	chr1:209886429-209886430	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs533182345	chr1:209886496-209886497	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs185952945	chr1:209886511-209886512	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs570074966	chr1:209886550-209886551	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs531516657	chr1:209886560-209886561	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs190610137	chr1:209886575-209886576	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs12138452	chr1:209886578-209886579	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs201286680	chr1:209886582-209886583	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs34755409	chr1:209886593-209886594	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs34038823	chr1:209886599-209886600	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Macular degeneration	22558131	CNVD
Alzheimer''s disease	21403675	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	17060936	CNVD
Atypical hemolytic uremic syndrome	19861685	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:234 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:209878600-209888200	Weak transcription	Brain Angular Gyrus	brain
2	chr1:209878800-209893400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr1:209881200-209886000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr1:209881400-209887200	Weak transcription	HMEC	breast
5	chr1:209882200-209887000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr1:209882400-209887000	Weak transcription	Brain Hippocampus Middle	brain
7	chr1:209882400-209887000	Weak transcription	Brain Substantia Nigra	brain
8	chr1:209882600-209886800	Weak transcription	Brain Cingulate Gyrus	brain
9	chr1:209883000-209887400	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr1:209883200-209886000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr1:209884000-209886000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr1:209884000-209889000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr1:209884400-209887400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr1:209884600-209886000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr1:209885000-209886200	Weak transcription	NHEK	skin
16	chr1:209885000-209886600	Weak transcription	Liver	Liver
17	chr1:209885000-209887200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr1:209885000-209888200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr1:209885200-209886400	Enhancers	HUVEC	blood vessel
20	chr1:209886000-209886200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr1:209886000-209886400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr1:209886000-209886400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr1:209886000-209886400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr1:209886000-209887400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr1:209886200-209886600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr1:209886200-209886600	Enhancers	NHEK	skin
27	chr1:209886400-209887400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr1:209886400-209893200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr1:209886400-209896400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr1:209886600-209888000	Weak transcription	NHEK	skin
31	chr1:209886600-209889000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr1:209886600-209889000	Strong transcription	Liver	Liver
33	chr1:209886800-209888400	Enhancers	Brain Cingulate Gyrus	brain
34	chr1:209887000-209889000	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr1:209887000-209889000	Enhancers	Brain Hippocampus Middle	brain
36	chr1:209887000-209889000	Enhancers	Brain Substantia Nigra	brain
37	chr1:209887200-209887400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr1:209887200-209887600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr1:209887200-209888200	Enhancers	HMEC	breast
40	chr1:209887400-209887600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr1:209887400-209888200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
42	chr1:209887400-209889000	Enhancers	Brain Inferior Temporal Lobe	brain
43	chr1:209887400-209889200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
44	chr1:209887600-209887800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr1:209887600-209888400	Enhancers	Brain Anterior Caudate	brain
46	chr1:209887600-209889200	Enhancers	Placenta Amnion	Placenta Amnion
47	chr1:209888000-209888200	Enhancers	Lung	lung
48	chr1:209888000-209888200	Enhancers	NHEK	skin
49	chr1:209888000-209888400	Enhancers	Placenta	Placenta
50	chr1:209888200-209888400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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