Variant report

Variant	esv18435
Chromosome Location	chr9:110584585-110604045
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:51)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:51 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr9:110594691-110594773	K562	blood:	n/a	n/a
2	BHLHE40	chr9:110589595-110589946	K562	blood:	n/a	n/a
3	BHLHE40	chr9:110589669-110589918	GM12878	blood:	n/a	n/a
4	CEBPB	chr9:110595727-110595955	IMR90	lung:	n/a	chr9:110595835-110595848 chr9:110595835-110595846
5	CEBPB	chr9:110588811-110588929	HepG2	liver:	n/a	chr9:110588854-110588865
6	CEBPB	chr9:110594007-110594140	K562	blood:	n/a	chr9:110594077-110594088
7	CEBPB	chr9:110593971-110594167	IMR90	lung:	n/a	chr9:110594077-110594088
8	CEBPB	chr9:110603507-110603697	A549	lung:	n/a	chr9:110603565-110603582 chr9:110603566-110603579 chr9:110603566-110603579
9	CEBPB	chr9:110588732-110589010	K562	blood:	n/a	chr9:110588854-110588865
10	CEBPB	chr9:110603519-110603601	Hela-S3	cervix:	n/a	chr9:110603565-110603582 chr9:110603566-110603579 chr9:110603566-110603579
11	CEBPB	chr9:110594036-110594174	HepG2	liver:	n/a	chr9:110594077-110594088
12	CEBPB	chr9:110588797-110588869	H1-hESC	embryonic stem cell:	n/a	chr9:110588854-110588865
13	CEBPB	chr9:110594013-110594213	A549	lung:	n/a	chr9:110594077-110594088
14	CTCF	chr9:110588580-110588730	AG04449	skin:	n/a	chr9:110588705-110588718
15	CTCF	chr9:110588580-110588730	HEK293	kidney:	n/a	chr9:110588705-110588718
16	CTCF	chr9:110588272-110588322	LNCaP	prostate:	n/a	n/a
17	CTCF	chr9:110588580-110588730	HMF	breast:	n/a	chr9:110588705-110588718
18	CTCF	chr9:110588600-110588750	HCPEpiC	choroid plexus:	n/a	chr9:110588705-110588718
19	CTCF	chr9:110588679-110588743	Hela-S3	cervix:	n/a	chr9:110588705-110588718
20	CTCF	chr9:110588580-110588730	HUVEC	blood vessel:	n/a	chr9:110588705-110588718
21	CTCF	chr9:110588265-110588268	LNCaP	prostate:	n/a	n/a
22	CTCF	chr9:110588540-110588690	HVMF	connective:	n/a	n/a
23	CTCF	chr9:110588520-110588670	HMF	breast:	n/a	n/a
24	CTCF	chr9:110588692-110588716	MCF-7	breast:	n/a	n/a
25	CTCF	chr9:110588681-110588721	HepG2	liver:	n/a	chr9:110588705-110588718
26	CTCF	chr9:110588660-110588810	HA-sp	spinal cord:	n/a	chr9:110588705-110588718
27	CTCF	chr9:110588620-110588770	HCPEpiC	choroid plexus:	n/a	chr9:110588705-110588718
28	CTCF	chr9:110588640-110588790	HFF	foreskin:	n/a	chr9:110588705-110588718
29	EBF1	chr9:110589698-110589941	GM12878	blood:	n/a	n/a
30	FOS	chr9:110595726-110595873	MCF10A-Er-Src	breast:	n/a	n/a
31	FOXA1	chr9:110598601-110598887	T-47D	breast:	n/a	n/a
32	IRF1	chr9:110588648-110588780	K562	blood:	n/a	n/a
33	JUND	chr9:110588931-110589274	K562	blood:	n/a	n/a
34	JUND	chr9:110589718-110589919	K562	blood:	n/a	n/a
35	MAFF	chr9:110588144-110588384	HepG2	liver:	n/a	chr9:110588274-110588292
36	MAFK	chr9:110588208-110588350	IMR90	lung:	n/a	n/a
37	MAFK	chr9:110588143-110588404	HepG2	liver:	n/a	n/a
38	MAFK	chr9:110587657-110587703	HepG2	liver:	n/a	n/a
39	MAFK	chr9:110588131-110588383	HepG2	liver:	n/a	n/a
40	MYC	chr9:110595690-110595847	MCF10A-Er-Src	breast:	n/a	n/a
41	POLR2A	chr9:110603340-110603711	MCF10A-Er-Src	breast:	n/a	n/a
42	POLR2A	chr9:110594250-110594450	Gliobla	brain:	n/a	n/a
43	POLR2A	chr9:110595393-110595535	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr9:110594186-110594240	HUVEC	blood vessel:	n/a	n/a
45	RAD21	chr9:110588656-110588839	Hela-S3	cervix:	n/a	chr9:110588701-110588720
46	RCOR1	chr9:110588968-110590023	K562	blood:	n/a	n/a
47	SMC3	chr9:110588628-110588740	Hela-S3	cervix:	n/a	chr9:110588705-110588719
48	STAT3	chr9:110586256-110586264	MCF10A-Er-Src	breast:	n/a	n/a
49	STAT3	chr9:110587061-110587070	MCF10A-Er-Src	breast:	n/a	n/a
50	STAT3	chr9:110592513-110592549	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:110595657-110595707	Caco-2	colon:	n/a
2	chr9:110595657-110595707	BJ	skin:	n/a
3	chr9:110595657-110595707	NHBE	bronchial:	n/a
4	chr9:110595657-110595707	AG10803	skin:	n/a
5	chr9:110595657-110595707	HUVEC	blood vessel:	n/a
6	chr9:110595657-110595707	AG09319	gingival:	n/a
7	chr9:110595657-110595707	PrEC	prostate:	n/a
8	chr9:110595657-110595707	NB4	blood:	n/a
9	chr9:110595657-110595707	GM19239	blood:	n/a
10	chr9:110595657-110595707	HRPEpiC	eye:	n/a
11	chr9:110595657-110595707	IMR90	lung:	fetal
12	chr9:110595657-110595707	RPTEC	kidney:	n/a
13	chr9:110595657-110595707	HL-60	blood:	n/a
14	chr9:110595657-110595707	NH-A	brain:	n/a
15	chr9:110595657-110595707	LNCaP	prostate:	n/a
16	chr9:110595657-110595707	PANC-1	pancreas:	n/a
17	chr9:110595657-110595707	PFSK-1	brain:	n/a
18	chr9:110595657-110595707	AG04449	skin:	fetal
19	chr9:110595657-110595707	SK-N-SH_RA	brain:	n/a
20	chr9:110595657-110595707	HEEpiC	esophagus:	n/a
21	chr9:110595657-110595707	T-47D	breast:	n/a
22	chr9:110595657-110595707	HEK293	kidney:	embryo
23	chr9:110595657-110595707	HCM	heart:	n/a
24	chr9:110595657-110595707	Jurkat	blood:	n/a
25	chr9:110595657-110595707	NT2-D1	testis:	n/a
26	chr9:110595657-110595707	GM06990	blood:	n/a
27	chr9:110595657-110595707	HCT-116	colon:	n/a
28	chr9:110595657-110595707	HMEC	breast:	n/a
29	chr9:110595657-110595707	HRE	kidney:	n/a
30	chr9:110595657-110595707	A549	lung:	n/a
31	chr9:110595657-110595707	ProgFib	skin:	n/a
32	chr9:110595657-110595707	ovcar-3	ovarian:	n/a
33	chr9:110595657-110595707	CMK	blood:	n/a
34	chr9:110595657-110595707	HAEpiC	amniotic membrane:	n/a
35	chr9:110595657-110595707	AG04450	lung:	fetal
36	chr9:110595657-110595707	HCF	heart:	n/a
37	chr9:110595657-110595707	SKMC	muscle:	n/a
38	chr9:110595657-110595707	ECC-1	luminal epithelium:	n/a
39	chr9:110595657-110595707	HRCEpiC	kidney:	n/a
40	chr9:110595657-110595707	HCPEpiC	choroid plexus:	n/a
41	chr9:110595657-110595707	Hepatocyte	liver:	n/a
42	chr9:110595657-110595707	Hela-S3	cervix:	n/a
43	chr9:110595657-110595707	SK-N-SH	brain:	n/a
44	chr9:110595657-110595707	H1-hESC	embryonic stem cell:	embryo
45	chr9:110595657-110595707	MCF-7	breast:	n/a
46	chr9:110595657-110595707	U87	brain:	n/a
47	chr9:110595657-110595707	GM12878	blood:	n/a
48	chr9:110595657-110595707	HPAEpiC	pulmonary alveolar:	n/a
49	chr9:110595657-110595707	NHDF-neo	bronchial:	n/a
50	chr9:110595657-110595707	GM12892	blood:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:110581417..110583396-chr9:110584777..110586664,2	K562	blood:
2	chr9:110581379..110584001-chr9:110585798..110587746,2	MCF-7	breast:
3	chr9:110501617..110503212-chr9:110597427..110600005,2	MCF-7	breast:
4	chr9:110249995..110252233-chr9:110582844..110585278,2	MCF-7	breast:
5	chr9:110602271..110604876-chr9:110605539..110607176,2	MCF-7	breast:
6	chr9:110599651..110602370-chr9:110609677..110611302,2	MCF-7	breast:

No data

Variant related genes	Relation type
RPL36AP6	TF binding region
RPL36AP6	CpG island
ENSG00000136826	chromatin interactions

Extended variants
information (count: 673 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145713891	chr9:110584595-110584596	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs577372716	chr9:110584620-110584621	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs544526953	chr9:110584627-110584628	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs561000658	chr9:110584640-110584641	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs563188127	chr9:110584696-110584697	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs191667094	chr9:110584703-110584704	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs556603263	chr9:110584716-110584717	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs75664461	chr9:110584735-110584736	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs145346907	chr9:110584740-110584741	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs371168501	chr9:110584800-110584801	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs12342292	chr9:110584807-110584808	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs183771076	chr9:110584842-110584843	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs551858049	chr9:110584845-110584846	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs570257333	chr9:110584854-110584855	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs546780808	chr9:110584856-110584857	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs531520760	chr9:110584857-110584858	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs543790991	chr9:110584876-110584877	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs75404038	chr9:110584936-110584937	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs568321223	chr9:110584945-110584946	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs527262603	chr9:110585093-110585094	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs142620417	chr9:110585098-110585099	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs12351548	chr9:110585100-110585101	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs188701935	chr9:110585180-110585181	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs148342798	chr9:110585203-110585204	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs559091227	chr9:110585212-110585213	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs577307008	chr9:110585243-110585244	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs572656070	chr9:110585286-110585287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs192651660	chr9:110585298-110585299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs10217391	chr9:110585299-110585300	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs373818853	chr9:110585309-110585310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs376247047	chr9:110585315-110585316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs182194547	chr9:110585330-110585331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs566344340	chr9:110585425-110585426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs555169242	chr9:110585448-110585449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs551913281	chr9:110585451-110585452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs377438771	chr9:110585452-110585453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs542126908	chr9:110585471-110585472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs559672558	chr9:110585505-110585506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs527284664	chr9:110585534-110585535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs369094877	chr9:110585566-110585567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs545431240	chr9:110585577-110585578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs12343543	chr9:110585598-110585599	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs186663698	chr9:110585600-110585601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs537047977	chr9:110585631-110585632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs150311297	chr9:110585649-110585650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568179384	chr9:110585667-110585668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs62570466	chr9:110585669-110585670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs191511282	chr9:110585732-110585733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs117914679	chr9:110585751-110585752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369016165	chr9:110585787-110585788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Fukuyama congenital muscular dystrophy	21572526	CNVD
Testicular germ cell tumor	18059402	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:110573200-110586400	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr9:110580400-110590800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr9:110581600-110585400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr9:110582400-110588200	Weak transcription	Placenta	Placenta
5	chr9:110582800-110589800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr9:110584000-110591000	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr9:110584200-110589800	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr9:110585400-110585600	Enhancers	H9 Cell Line	embryonic stem cell
9	chr9:110586000-110586600	Enhancers	Colon Smooth Muscle	Colon
10	chr9:110586000-110586800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr9:110586000-110586800	Bivalent Enhancer	Fetal Lung	lung
12	chr9:110586400-110586800	Enhancers	Duodenum Smooth Muscle	Duodenum
13	chr9:110586400-110587200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr9:110588200-110588400	Enhancers	Sigmoid Colon	Sigmoid Colon
15	chr9:110588200-110590000	Enhancers	Placenta	Placenta
16	chr9:110588400-110589400	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr9:110589200-110590000	Enhancers	K562	blood
18	chr9:110589200-110590400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr9:110589400-110590800	Enhancers	Sigmoid Colon	Sigmoid Colon
20	chr9:110589800-110590000	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr9:110589800-110590200	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr9:110591000-110591400	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr9:110594400-110594600	Enhancers	Esophagus	oesophagus
24	chr9:110594800-110596400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr9:110595200-110596200	Enhancers	Fetal Lung	lung
26	chr9:110595200-110596400	Enhancers	Adipose Nuclei	Adipose
27	chr9:110595400-110595800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr9:110595400-110596400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr9:110595400-110596400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr9:110595600-110596200	Enhancers	NHDF-Ad	bronchial
31	chr9:110596400-110601000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr9:110596400-110601800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr9:110601000-110601400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr9:110601000-110602800	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr9:110601000-110605200	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr9:110601400-110602200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr9:110601600-110602000	Enhancers	Brain Hippocampus Middle	brain
38	chr9:110601800-110602200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr9:110602200-110602400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr9:110602200-110602800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr9:110602400-110602800	Enhancers	Ovary	ovary
42	chr9:110602400-110603800	Enhancers	Adipose Nuclei	Adipose
43	chr9:110602800-110603800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr9:110602800-110604600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
45	chr9:110603200-110603400	Enhancers	Primary B cells from cord blood	blood
46	chr9:110603200-110604000	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr9:110603200-110604200	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr9:110603800-110604000	Weak transcription	Primary B cells from cord blood	blood

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