Variant report

Variant	nsv599617
Chromosome Location	chr5:120608476-120670292
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	ATF1	chr5:120609797-120610099	K562	blood:	n/a	n/a
2	ATF3	chr5:120609660-120610180	A549	lung:	n/a	n/a
3	ATF3	chr5:120609671-120610135	A549	lung:	n/a	n/a
4	BACH1	chr5:120609897-120610216	K562	blood:	n/a	n/a
5	BCL3	chr5:120609574-120610233	A549	lung:	n/a	n/a
6	BCL3	chr5:120609611-120610175	A549	lung:	n/a	n/a
7	CBX3	chr5:120609626-120610276	HCT-116	colon:	n/a	n/a
8	CEBPB	chr5:120640558-120640915	IMR90	lung:	n/a	chr5:120640725-120640734 chr5:120640725-120640734 chr5:120640723-120640736 chr5:120640723-120640736 chr5:120640720-120640737 chr5:120640723-120640734 chr5:120640793-120640806 chr5:120640725-120640734
9	CEBPB	chr5:120665137-120665399	H1-hESC	embryonic stem cell:	n/a	chr5:120665251-120665262 chr5:120665252-120665263 chr5:120665253-120665262
10	CEBPB	chr5:120650749-120651103	K562	blood:	n/a	n/a
11	CEBPB	chr5:120640581-120640914	A549	lung:	n/a	chr5:120640725-120640734 chr5:120640725-120640734 chr5:120640723-120640736 chr5:120640723-120640736 chr5:120640720-120640737 chr5:120640723-120640734 chr5:120640793-120640806 chr5:120640725-120640734
12	CEBPB	chr5:120650738-120651081	IMR90	lung:	n/a	n/a
13	CEBPB	chr5:120665091-120665434	K562	blood:	n/a	chr5:120665251-120665262 chr5:120665252-120665263 chr5:120665253-120665262
14	CEBPB	chr5:120640581-120640927	A549	lung:	n/a	chr5:120640725-120640734 chr5:120640725-120640734 chr5:120640723-120640736 chr5:120640723-120640736 chr5:120640720-120640737 chr5:120640723-120640734 chr5:120640793-120640806 chr5:120640725-120640734
15	CEBPB	chr5:120650741-120651097	A549	lung:	n/a	n/a
16	CEBPB	chr5:120640554-120640918	ECC-1	luminal epithelium:	n/a	chr5:120640725-120640734 chr5:120640725-120640734 chr5:120640723-120640736 chr5:120640723-120640736 chr5:120640720-120640737 chr5:120640723-120640734 chr5:120640793-120640806 chr5:120640725-120640734
17	CEBPB	chr5:120609529-120610117	A549	lung:	n/a	chr5:120609623-120609636
18	CEBPB	chr5:120640568-120640898	H1-hESC	embryonic stem cell:	n/a	chr5:120640725-120640734 chr5:120640725-120640734 chr5:120640723-120640736 chr5:120640723-120640736 chr5:120640720-120640737 chr5:120640723-120640734 chr5:120640793-120640806 chr5:120640725-120640734
19	CEBPB	chr5:120665080-120665327	A549	lung:	n/a	chr5:120665251-120665262 chr5:120665252-120665263 chr5:120665253-120665262
20	CEBPB	chr5:120650883-120651016	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr5:120615503-120615753	K562	blood:	n/a	n/a
22	CEBPB	chr5:120609534-120610174	Hela-S3	cervix:	n/a	chr5:120609623-120609636
23	CEBPB	chr5:120650738-120651104	HepG2	liver:	n/a	n/a
24	CEBPB	chr5:120615541-120615802	K562	blood:	n/a	n/a
25	CEBPB	chr5:120640550-120640906	HepG2	liver:	n/a	chr5:120640725-120640734 chr5:120640725-120640734 chr5:120640723-120640736 chr5:120640723-120640736 chr5:120640720-120640737 chr5:120640723-120640734 chr5:120640793-120640806 chr5:120640725-120640734
26	CEBPB	chr5:120650781-120651061	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr5:120640581-120640912	Hela-S3	cervix:	n/a	chr5:120640725-120640734 chr5:120640725-120640734 chr5:120640723-120640736 chr5:120640723-120640736 chr5:120640720-120640737 chr5:120640723-120640734 chr5:120640793-120640806 chr5:120640725-120640734
28	CEBPB	chr5:120609521-120610150	IMR90	lung:	n/a	chr5:120609623-120609636
29	CEBPB	chr5:120640491-120640969	A549	lung:	n/a	chr5:120640725-120640734 chr5:120640725-120640734 chr5:120640723-120640736 chr5:120640723-120640736 chr5:120640720-120640737 chr5:120640723-120640734 chr5:120640793-120640806 chr5:120640725-120640734
30	CEBPB	chr5:120640541-120640899	K562	blood:	n/a	chr5:120640725-120640734 chr5:120640725-120640734 chr5:120640723-120640736 chr5:120640723-120640736 chr5:120640720-120640737 chr5:120640723-120640734 chr5:120640793-120640806 chr5:120640725-120640734
31	CEBPB	chr5:120665178-120665393	Hela-S3	cervix:	n/a	chr5:120665251-120665262 chr5:120665252-120665263 chr5:120665253-120665262
32	CEBPB	chr5:120609455-120610277	A549	lung:	n/a	chr5:120609623-120609636
33	CEBPB	chr5:120665093-120665414	IMR90	lung:	n/a	chr5:120665251-120665262 chr5:120665252-120665263 chr5:120665253-120665262
34	CEBPB	chr5:120628443-120628634	K562	blood:	n/a	chr5:120628524-120628535
35	CEBPB	chr5:120665120-120665392	HepG2	liver:	n/a	chr5:120665251-120665262 chr5:120665252-120665263 chr5:120665253-120665262
36	CEBPD	chr5:120615370-120615697	K562	blood:	n/a	n/a
37	CHD2	chr5:120609726-120610137	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr5:120618420-120618570	GM12866	blood:	n/a	n/a
39	CTCF	chr5:120669952-120670015	GM10266	blood:	n/a	n/a
40	CTCF	chr5:120663389-120663435	Fibrobl	skin:	n/a	n/a
41	E2F4	chr5:120648717-120649023	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr5:120613710-120613833	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr5:120642910-120643161	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr5:120609819-120610215	MCF10A-Er-Src	breast:	n/a	n/a
45	EBF1	chr5:120621396-120621661	GM12878	blood:	n/a	n/a
46	EGR1	chr5:120609777-120609994	K562	blood:	n/a	n/a
47	ELF1	chr5:120609793-120610088	A549	lung:	n/a	n/a
48	EP300	chr5:120609465-120610409	A549	lung:	n/a	n/a
49	EP300	chr5:120609609-120610149	Hela-S3	cervix:	n/a	n/a
50	EP300	chr5:120609429-120610371	A549	lung:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:120643239..120645271-chr5:120645522..120647194,2	K562	blood:
2	chr5:120631738..120633506-chr5:120633517..120635841,2	K562	blood:
3	chr5:120643239..120645271-chr5:120645522..120647194,2	K562	blood:
4	chr5:120628569..120631260-chr5:120631938..120634860,2	MCF-7	breast:
5	chr5:120631738..120633506-chr5:120633517..120635841,2	K562	blood:
6	chr5:120621053..120623969-chr5:120627723..120630035,2	MCF-7	breast:
7	chr5:120628569..120631260-chr5:120631938..120634860,2	MCF-7	breast:
8	chr5:120604790..120607005-chr5:120607199..120609992,2	K562	blood:
9	chr5:120621053..120623969-chr5:120627723..120630035,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FTMT-2	chr5:120659736-120659765	ENSG00000229855.4
2	lnc-FTMT-2	chr5:120658244-120658302	NONHSAT103454
3	lnc-FTMT-2	chr5:120656659-120656681	NONHSAT103454
4	lnc-FTMT-2	chr5:120658245-120658302	XLOC_004529
5	lnc-FTMT-2	chr5:120649672-120649899	ENSG00000229855.4
6	lnc-FTMT-2	chr5:120661117-120661175	ENSG00000229855.4
7	lnc-FTMT-2	chr5:120656575-120656681	ENSG00000229855.4
8	lnc-FTMT-2	chr5:120658249-120658302	ENSG00000229855.4
9	lnc-FTMT-2	chr5:120661041-120661595	NONHSAT103454
10	lnc-FTMT-2	chr5:120659733-120659765	NONHSAT103454
11	lnc-FTMT-2	chr5:120658249-120658302	ENSG00000229855.4
12	lnc-FTMT-2	chr5:120661117-120661532	XLOC_004529
13	lnc-FTMT-2	chr5:120649656-120649899	ENSG00000229855.4
14	lnc-FTMT-2	chr5:120661117-120661793	ENSG00000229855.4
15	lnc-FTMT-2	chr5:120659736-120659765	XLOC_004529
16	lnc-FTMT-2	chr5:120661117-120661651	ENSG00000229855.4
17	lnc-FTMT-2	chr5:120656575-120656681	ENSG00000229855.4
18	lnc-FTMT-2	chr5:120658249-120658302	ENSG00000229855.4
19	lnc-FTMT-2	chr5:120661122-120661174	ENSG00000229855.4
20	lnc-FTMT-2	chr5:120658245-120658302	ENSG00000229855.4
21	lnc-FTMT-2	chr5:120621476-120621568	ENSG00000229855.4
22	lnc-FTMT-2	chr5:120659736-120659765	ENSG00000229855.4

Variant related genes	Relation type
ENSG00000229855	TF binding region

Extended variants
information (count: 1396 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1396 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12188286	chr5:120608476-120608477	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs540010532	chr5:120608485-120608486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs558813939	chr5:120608499-120608500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537619904	chr5:120608512-120608513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs17147535	chr5:120608516-120608517	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs73276548	chr5:120608532-120608533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs187025598	chr5:120608557-120608558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538682013	chr5:120608559-120608560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530181507	chr5:120608579-120608580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs112473359	chr5:120608614-120608615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs57395948	chr5:120608619-120608620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs534135247	chr5:120608649-120608650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs541912444	chr5:120608689-120608690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141685692	chr5:120608693-120608694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553828480	chr5:120608695-120608696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs114965254	chr5:120608704-120608705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571139395	chr5:120608726-120608727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs540973879	chr5:120608727-120608728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs550621973	chr5:120608732-120608733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs12188297	chr5:120608739-120608740	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs375484867	chr5:120608753-120608754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs150104323	chr5:120608760-120608761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554656569	chr5:120608791-120608792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs566394989	chr5:120608800-120608801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs190660257	chr5:120608816-120608817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs574211613	chr5:120608822-120608823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs534010553	chr5:120608837-120608838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs558459110	chr5:120608851-120608852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs181520667	chr5:120608859-120608860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs537747249	chr5:120608874-120608875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs185764254	chr5:120608920-120608921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs3943930	chr5:120608938-120608939	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs563068490	chr5:120608942-120608943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541775476	chr5:120608999-120609000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs560657500	chr5:120609002-120609003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs190186657	chr5:120609003-120609004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182685087	chr5:120609008-120609009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551420219	chr5:120609010-120609011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187858993	chr5:120609011-120609012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs143003264	chr5:120609016-120609017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs532090754	chr5:120609027-120609028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs560154602	chr5:120609064-120609065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550484451	chr5:120609076-120609077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs562325538	chr5:120609078-120609079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529715084	chr5:120609103-120609104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547845300	chr5:120609110-120609111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566598828	chr5:120609134-120609135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533632937	chr5:120609152-120609153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552397593	chr5:120609157-120609158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs570305633	chr5:120609175-120609176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:120600800-120609600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr5:120601400-120609200	Weak transcription	A549	lung
3	chr5:120609200-120609600	Enhancers	A549	lung
4	chr5:120609200-120609800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr5:120609400-120609600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr5:120609400-120609600	Enhancers	Muscle Satellite Cultured Cells	--
7	chr5:120609400-120609600	Enhancers	NHDF-Ad	bronchial
8	chr5:120609400-120609800	Enhancers	Osteobl	bone
9	chr5:120609600-120609800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
10	chr5:120609600-120610000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr5:120609600-120610000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr5:120609600-120610000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr5:120609600-120610000	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr5:120609600-120610000	Flanking Active TSS	NHDF-Ad	bronchial
15	chr5:120609600-120610200	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr5:120609600-120610200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr5:120609600-120610200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr5:120609600-120610200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr5:120609600-120610200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr5:120609600-120610200	Flanking Active TSS	A549	lung
21	chr5:120609600-120610200	Enhancers	Dnd41	blood
22	chr5:120609600-120610200	Enhancers	K562	blood
23	chr5:120609600-120610200	Enhancers	NHLF	lung
24	chr5:120609600-120610400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr5:120609600-120610400	Enhancers	Hela-S3	cervix
26	chr5:120609600-120610400	Enhancers	HMEC	breast
27	chr5:120609600-120610400	Enhancers	NH-A	brain
28	chr5:120609600-120610600	Enhancers	HUVEC	blood vessel
29	chr5:120609800-120610000	Enhancers	Muscle Satellite Cultured Cells	--
30	chr5:120609800-120610200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr5:120609800-120610200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr5:120609800-120610200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr5:120609800-120610200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr5:120609800-120610200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr5:120609800-120610200	Flanking Active TSS	Osteobl	bone
36	chr5:120610000-120610200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr5:120610000-120610200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr5:120610000-120610200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
39	chr5:120610000-120610400	Enhancers	NHDF-Ad	bronchial
40	chr5:120610200-120610400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr5:120610200-120610400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr5:120610200-120610400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr5:120610200-120610400	Enhancers	Muscle Satellite Cultured Cells	--
44	chr5:120610200-120610400	Enhancers	Osteobl	bone
45	chr5:120610200-120613000	Weak transcription	Dnd41	blood
46	chr5:120613000-120614400	Enhancers	Dnd41	blood
47	chr5:120621000-120621400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr5:120621000-120631200	Enhancers	Dnd41	blood
49	chr5:120621200-120621400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr5:120621200-120622400	Enhancers	Adipose Nuclei	Adipose

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links