Variant report

Variant	esv1793845
Chromosome Location	chr3:20207023-20219694
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:50)
CpG islands
(count:0)
Chromatin interactive
region (count:22)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr3:20208029-20208263	Hela-S3	cervix:	n/a	chr3:20208153-20208164
2	CEBPB	chr3:20207974-20208344	IMR90	lung:	n/a	chr3:20208153-20208164
3	CEBPB	chr3:20208111-20208315	H1-hESC	embryonic stem cell:	n/a	chr3:20208153-20208164
4	CEBPB	chr3:20207983-20208309	HepG2	liver:	n/a	chr3:20208153-20208164
5	CEBPB	chr3:20207973-20208334	A549	lung:	n/a	chr3:20208153-20208164
6	CEBPB	chr3:20207984-20208313	K562	blood:	n/a	chr3:20208153-20208164
7	CEBPB	chr3:20208038-20208329	MCF-7	breast:	n/a	chr3:20208153-20208164
8	EBF1	chr3:20215299-20215687	GM12878	blood:	n/a	chr3:20215478-20215489 chr3:20215477-20215490
9	EBF1	chr3:20215321-20215600	GM12878	blood:	n/a	chr3:20215478-20215489 chr3:20215477-20215490
10	EP300	chr3:20218800-20219102	SK-N-SH_RA	brain:	n/a	n/a
11	EP300	chr3:20218811-20219127	SK-N-SH_RA	brain:	n/a	n/a
12	JUN	chr3:20213379-20213565	K562	blood:	n/a	n/a
13	JUN	chr3:20215318-20215388	K562	blood:	n/a	n/a
14	MXI1	chr3:20210973-20211122	K562	blood:	n/a	n/a
15	MYC	chr3:20209482-20209682	MCF10A-Er-Src	breast:	n/a	n/a
16	NFYB	chr3:20215663-20215848	Hela-S3	cervix:	n/a	n/a
17	POLR2A	chr3:20218540-20218548	MCF-7	breast:	n/a	n/a
18	POLR2A	chr3:20210418-20211485	K562	blood:	n/a	n/a
19	POLR2A	chr3:20213694-20213790	MCF-7	breast:	n/a	n/a
20	POLR2A	chr3:20215458-20216639	K562	blood:	n/a	n/a
21	POLR2A	chr3:20213630-20213635	MCF-7	breast:	n/a	n/a
22	POLR2A	chr3:20215519-20215895	A549	lung:	n/a	n/a
23	POLR2A	chr3:20217466-20217657	MCF-7	breast:	n/a	n/a
24	POLR2A	chr3:20211682-20211703	MCF-7	breast:	n/a	n/a
25	POLR2A	chr3:20216235-20216435	GM12878	blood:	n/a	n/a
26	POLR2A	chr3:20211814-20211824	MCF-7	breast:	n/a	n/a
27	POLR2A	chr3:20216395-20216444	MCF10A-Er-Src	breast:	n/a	n/a
28	POLR2A	chr3:20214312-20214368	MCF-7	breast:	n/a	n/a
29	POLR2A	chr3:20218958-20219093	MCF-7	breast:	n/a	n/a
30	POLR2A	chr3:20207445-20207517	HepG2	liver:	n/a	n/a
31	POLR2A	chr3:20209699-20209792	HepG2	liver:	n/a	n/a
32	POLR2A	chr3:20209941-20210046	MCF10A-Er-Src	breast:	n/a	n/a
33	POLR2A	chr3:20213717-20213827	MCF-7	breast:	n/a	n/a
34	POLR2A	chr3:20218980-20219130	MCF10A-Er-Src	breast:	n/a	n/a
35	POLR2A	chr3:20215751-20215987	Hela-S3	cervix:	n/a	n/a
36	POLR2A	chr3:20211616-20211625	MCF-7	breast:	n/a	n/a
37	POLR2A	chr3:20218289-20218489	MCF10A-Er-Src	breast:	n/a	n/a
38	POLR2A	chr3:20206469-20207165	K562	blood:	n/a	n/a
39	POLR2A	chr3:20211722-20211777	MCF-7	breast:	n/a	n/a
40	POLR2A	chr3:20207757-20208179	K562	blood:	n/a	n/a
41	POLR2A	chr3:20209182-20209323	MCF-7	breast:	n/a	n/a
42	POLR2A	chr3:20213320-20213383	MCF10A-Er-Src	breast:	n/a	n/a
43	POLR2A	chr3:20214533-20214660	K562	blood:	n/a	n/a
44	POLR2A	chr3:20214224-20214244	MCF-7	breast:	n/a	n/a
45	POLR2A	chr3:20213734-20213797	MCF-7	breast:	n/a	n/a
46	RFX5	chr3:20218274-20218561	K562	blood:	n/a	n/a
47	STAT3	chr3:20207872-20208171	MCF10A-Er-Src	breast:	n/a	chr3:20208132-20208143
48	STAT3	chr3:20208062-20208161	MCF10A-Er-Src	breast:	n/a	chr3:20208132-20208143
49	STAT3	chr3:20213229-20213429	MCF10A-Er-Src	breast:	n/a	n/a
50	STAT3	chr3:20215551-20215628	MCF10A-Er-Src	breast:	n/a	n/a

No data

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:20218894..20221253-chr3:20226177..20229116,2	MCF-7	breast:
2	chr3:20216479..20218064-chr3:20218704..20221260,2	K562	blood:
3	chr3:20213813..20216501-chr3:20227432..20229116,2	MCF-7	breast:
4	chr3:19986817..19988952-chr3:20217097..20219211,2	K562	blood:
5	chr3:20215671..20219222-chr3:20225067..20228168,4	MCF-7	breast:
6	chr3:20219250..20222131-chr3:20228592..20230370,2	K562	blood:
7	chr3:20080586..20082828-chr3:20216112..20219264,3	K562	blood:
8	chr3:20200366..20203372-chr3:20209857..20212107,3	K562	blood:
9	chr3:20210669..20212300-chr3:20217697..20220649,2	K562	blood:
10	chr3:20197127..20199080-chr3:20208900..20210840,2	MCF-7	breast:
11	chr3:20208211..20212087-chr3:20224920..20227676,5	K562	blood:
12	chr3:20211282..20213997-chr3:20225429..20228054,3	MCF-7	breast:
13	chr3:20210669..20212300-chr3:20217697..20220649,2	K562	blood:
14	chr3:20212661..20217850-chr3:20224065..20229766,9	K562	blood:
15	chr3:20193485..20196421-chr3:20205590..20208525,2	K562	blood:
16	chr3:20206092..20207782-chr3:20216460..20218892,2	K562	blood:
17	chr3:20216479..20218064-chr3:20218704..20221260,2	K562	blood:
18	chr3:20209340..20212001-chr3:20214407..20216140,2	K562	blood:
19	chr3:20188319..20191715-chr3:20218902..20221810,3	K562	blood:
20	chr3:20206092..20207782-chr3:20216460..20218892,2	K562	blood:
21	chr3:20079993..20081743-chr3:20205055..20207823,2	MCF-7	breast:
22	chr3:20212391..20215096-chr3:20215867..20218986,3	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KAT2B-1	chr3:20216227-20216310	ENSG00000237485.1
2	lnc-KAT2B-1	chr3:20215736-20216017	ENSG00000237485.1
3	lnc-KAT2B-5	chr3:20210846-20210905	l_2328_chr3:20202875-20210905_testes
4	lnc-KAT2B-1	chr3:20218709-20218742	ENSG00000237485.1
5	lnc-PP2D1-2	chr3:20212535-20212759	NONHSAT088614
6	lnc-KAT2B-1	chr3:20216227-20216310	ENSG00000237485.1
7	lnc-PP2D1-2	chr3:20211553-20212307	NONHSAT088614
8	lnc-KAT2B-1	chr3:20215778-20216017	ENSG00000237485.1

No data

Variant related genes	Relation type
SGOL1-AS1	TF binding region
SGOL1	TF binding region
ENSG00000163576	chromatin interactions
ENSG00000144566	chromatin interactions
ENSG00000129810	chromatin interactions
ENSG00000114166	chromatin interactions
ENSG00000237485	chromatin interactions

Extended variants
information (count: 481 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:481 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6793304	chr3:20207023-20207024	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs143170864	chr3:20207074-20207075	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs370279639	chr3:20207084-20207085	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs544916475	chr3:20207103-20207104	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs187702378	chr3:20207127-20207128	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs527518730	chr3:20207129-20207130	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs9849205	chr3:20207136-20207137	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs111545032	chr3:20207269-20207270	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs369465702	chr3:20207270-20207271	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs531844303	chr3:20207282-20207283	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs4858772	chr3:20207293-20207294	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs192621021	chr3:20207296-20207297	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs532821064	chr3:20207450-20207451	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs62241673	chr3:20207459-20207460	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs145171613	chr3:20207472-20207473	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs369890358	chr3:20207499-20207500	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs536486950	chr3:20207501-20207502	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs111831268	chr3:20207517-20207518	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs200905225	chr3:20207522-20207523	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs183368678	chr3:20207623-20207624	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs187748546	chr3:20207628-20207629	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs558680839	chr3:20207634-20207635	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs572704538	chr3:20207678-20207679	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs537568796	chr3:20207710-20207711	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs555703464	chr3:20207719-20207720	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs577250075	chr3:20207745-20207746	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs544878448	chr3:20207788-20207789	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs376626307	chr3:20207790-20207791	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs9830249	chr3:20207811-20207812	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs559945037	chr3:20207838-20207839	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs148702338	chr3:20207842-20207843	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs71316250	chr3:20207873-20207874	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs76315194	chr3:20207905-20207906	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561141826	chr3:20207924-20207925	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs531683916	chr3:20207938-20207939	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs374784248	chr3:20207943-20207944	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs543950757	chr3:20207949-20207950	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs565264379	chr3:20207997-20207998	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs61171008	chr3:20208037-20208038	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs55794899	chr3:20208106-20208107	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs547352211	chr3:20208121-20208122	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs142214522	chr3:20208133-20208134	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs192367911	chr3:20208222-20208223	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs9854684	chr3:20208267-20208268	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs200939736	chr3:20208272-20208273	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs184703731	chr3:20208275-20208276	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs537529716	chr3:20208329-20208330	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs59883028	chr3:20208363-20208364	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs58288144	chr3:20208364-20208365	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs549489710	chr3:20208431-20208432	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Developmental delay	21147756	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Cancer	20164919	CNVD

Chromatin state (count:180 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:20141200-20222400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr3:20164800-20211400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr3:20167800-20226000	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr3:20184600-20220200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr3:20188400-20212400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr3:20190600-20220200	Weak transcription	Fetal Muscle Leg	muscle
7	chr3:20192800-20220600	Weak transcription	Fetal Lung	lung
8	chr3:20193800-20226600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr3:20194000-20220400	Weak transcription	NH-A	brain
10	chr3:20194800-20215200	Weak transcription	HepG2	liver
11	chr3:20195000-20212400	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr3:20195000-20226000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr3:20195200-20221800	Weak transcription	NHEK	skin
14	chr3:20195400-20226000	Weak transcription	NHDF-Ad	bronchial
15	chr3:20195400-20226200	Weak transcription	NHLF	lung
16	chr3:20195600-20212000	Weak transcription	Primary neutrophils fromperipheralblood	blood
17	chr3:20196400-20225600	Strong transcription	HUES64 Cell Line	embryonic stem cell
18	chr3:20196800-20221600	Weak transcription	Fetal Intestine Small	intestine
19	chr3:20197000-20226200	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr3:20197000-20226800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr3:20197400-20227000	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr3:20197600-20226800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr3:20198200-20219800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr3:20198600-20220200	Weak transcription	Thymus	Thymus
25	chr3:20199400-20225400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
26	chr3:20199600-20221000	Weak transcription	Fetal Stomach	stomach
27	chr3:20199600-20225400	Strong transcription	HUES48 Cell Line	embryonic stem cell
28	chr3:20200000-20225800	Weak transcription	Osteobl	bone
29	chr3:20201600-20209800	Weak transcription	HSMM	muscle
30	chr3:20201800-20220000	Weak transcription	Fetal Muscle Trunk	muscle
31	chr3:20201800-20225800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr3:20202000-20207400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr3:20202000-20209400	Weak transcription	Hela-S3	cervix
34	chr3:20202000-20212000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr3:20202200-20212000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr3:20202600-20215600	Weak transcription	GM12878-XiMat	blood
37	chr3:20202600-20216200	Weak transcription	Primary hematopoietic stem cells	blood
38	chr3:20202600-20226400	Weak transcription	Fetal Intestine Large	intestine
39	chr3:20202800-20209600	Weak transcription	Monocytes-CD14+_RO01746	blood
40	chr3:20202800-20210400	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr3:20203400-20212000	Weak transcription	HMEC	breast
42	chr3:20203800-20210600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr3:20203800-20215400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr3:20203800-20215600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr3:20204000-20207200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr3:20204000-20208200	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr3:20204000-20209200	Weak transcription	A549	lung
48	chr3:20204000-20209800	Weak transcription	Fetal Thymus	thymus
49	chr3:20204000-20210200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr3:20205000-20210600	Weak transcription	Cortex derived primary cultured neurospheres	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links