Variant report

Variant	esv3415147
Chromosome Location	chr3:42638848-42641746
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:431)
CpG islands
(count:61)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:431 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:42641666-42642344	HepG2	liver:	n/a	n/a
2	ATF1	chr3:42641654-42642337	K562	blood:	n/a	n/a
3	ATF2	chr3:42641592-42642442	GM12878	blood:	n/a	n/a
4	ATF2	chr3:42641620-42642361	GM12878	blood:	n/a	n/a
5	ATF2	chr3:42641542-42642369	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr3:42641454-42642367	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr3:42641646-42643028	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr3:42641569-42642257	GM12878	blood:	n/a	n/a
9	BCLAF1	chr3:42641579-42642437	GM12878	blood:	n/a	n/a
10	BCLAF1	chr3:42641430-42642375	GM12878	blood:	n/a	n/a
11	BHLHE40	chr3:42641609-42642497	HepG2	liver:	n/a	n/a
12	BHLHE40	chr3:42641481-42642847	K562	blood:	n/a	n/a
13	BHLHE40	chr3:42641525-42643096	GM12878	blood:	n/a	n/a
14	BRCA1	chr3:42641636-42642410	HepG2	liver:	n/a	n/a
15	BRCA1	chr3:42641537-42642381	H1-hESC	embryonic stem cell:	n/a	n/a
16	BRCA1	chr3:42641286-42642962	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr3:42641437-42642375	GM12878	blood:	n/a	n/a
18	CBX3	chr3:42641427-42643007	K562	blood:	n/a	n/a
19	CBX3	chr3:42641513-42642409	K562	blood:	n/a	n/a
20	CCNT2	chr3:42641603-42642923	K562	blood:	n/a	n/a
21	CEBPB	chr3:42641411-42642353	GM12878	blood:	n/a	n/a
22	CEBPB	chr3:42641421-42642298	Hela-S3	cervix:	n/a	n/a
23	CEBPD	chr3:42641693-42642225	HepG2	liver:	n/a	n/a
24	CEBPD	chr3:42641535-42642858	K562	blood:	n/a	n/a
25	CHD1	chr3:42641365-42641842	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr3:42641418-42642908	GM12878	blood:	n/a	n/a
27	CHD2	chr3:42641545-42642612	HepG2	liver:	n/a	n/a
28	CHD2	chr3:42641463-42642919	K562	blood:	n/a	n/a
29	CHD2	chr3:42641310-42642891	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr3:42641429-42642969	Hela-S3	cervix:	n/a	n/a
31	CREB1	chr3:42641554-42642727	GM12878	blood:	n/a	n/a
32	CREB1	chr3:42641639-42642462	H1-hESC	embryonic stem cell:	n/a	n/a
33	CREB1	chr3:42641516-42642424	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr3:42641724-42642448	A549	lung:	n/a	n/a
35	CTCF	chr3:42641591-42642403	K562	blood:	n/a	n/a
36	E2F4	chr3:42641136-42642309	MCF10A-Er-Src	breast:	n/a	chr3:42641918-42641927
37	E2F4	chr3:42641736-42642121	GM12878	blood:	n/a	chr3:42641918-42641927
38	E2F4	chr3:42641725-42642948	K562	blood:	n/a	chr3:42642320-42642332 chr3:42641918-42641927
39	E2F6	chr3:42641621-42642947	K562	blood:	n/a	chr3:42642320-42642332 chr3:42641918-42641927 chr3:42642321-42642332
40	E2F6	chr3:42641608-42641951	K562	blood:	n/a	chr3:42641918-42641927
41	E2F6	chr3:42641649-42642465	A549	lung:	n/a	chr3:42642320-42642332 chr3:42641918-42641927 chr3:42642321-42642332
42	E2F6	chr3:42641374-42642585	H1-hESC	embryonic stem cell:	n/a	chr3:42642320-42642332 chr3:42641918-42641927 chr3:42642321-42642332
43	E2F6	chr3:42641592-42642621	H1-hESC	embryonic stem cell:	n/a	chr3:42642320-42642332 chr3:42641918-42641927 chr3:42642321-42642332
44	EBF1	chr3:42641667-42642243	GM12878	blood:	n/a	n/a
45	EGR1	chr3:42641730-42642519	GM12878	blood:	n/a	chr3:42641918-42641927 chr3:42642289-42642298 chr3:42642165-42642179
46	EGR1	chr3:42641714-42642834	K562	blood:	n/a	chr3:42641918-42641927 chr3:42642289-42642298 chr3:42642165-42642179
47	EGR1	chr3:42641637-42642912	K562	blood:	n/a	chr3:42641918-42641927 chr3:42642289-42642298 chr3:42642165-42642179
48	EGR1	chr3:42641746-42642387	MCF-7	breast:	n/a	chr3:42641918-42641927 chr3:42642289-42642298 chr3:42642165-42642179
49	EGR1	chr3:42641487-42642965	HCT-116	colon:	n/a	chr3:42641918-42641927 chr3:42642289-42642298 chr3:42642165-42642179
50	EGR1	chr3:42641731-42642524	H1-hESC	embryonic stem cell:	n/a	chr3:42641918-42641927 chr3:42642289-42642298 chr3:42642165-42642179

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:42641690-42641740	SAEC	small airway:	n/a
2	chr3:42641690-42641740	NH-A	brain:	n/a
3	chr3:42641690-42641740	T-47D	breast:	n/a
4	chr3:42641690-42641740	Hepatocyte	liver:	n/a
5	chr3:42641690-42641740	GM12878	blood:	n/a
6	chr3:42641690-42641740	H1-hESC	embryonic stem cell:	embryo
7	chr3:42641690-42641740	HRE	kidney:	n/a
8	chr3:42641690-42641740	AG04450	lung:	fetal
9	chr3:42641690-42641740	AG10803	skin:	n/a
10	chr3:42641690-42641740	ProgFib	skin:	n/a
11	chr3:42641690-42641740	SKMC	muscle:	n/a
12	chr3:42641690-42641740	HRPEpiC	eye:	n/a
13	chr3:42641690-42641740	HPAEpiC	pulmonary alveolar:	n/a
14	chr3:42641690-42641740	AG09319	gingival:	n/a
15	chr3:42641690-42641740	GM19239	blood:	n/a
16	chr3:42641690-42641740	PFSK-1	brain:	n/a
17	chr3:42641690-42641740	RPTEC	kidney:	n/a
18	chr3:42641690-42641740	BE2_C	brain:	n/a
19	chr3:42641690-42641740	HRCEpiC	kidney:	n/a
20	chr3:42641690-42641740	Hela-S3	cervix:	n/a
21	chr3:42641690-42641740	HMEC	breast:	n/a
22	chr3:42641690-42641740	HNPCEpiC	eye:	n/a
23	chr3:42641690-42641740	AoSMC	blood vessel:	n/a
24	chr3:42641690-42641740	HL-60	blood:	n/a
25	chr3:42641690-42641740	U87	brain:	n/a
26	chr3:42641690-42641740	BJ	skin:	n/a
27	chr3:42641690-42641740	HCM	heart:	n/a
28	chr3:42641690-42641740	NB4	blood:	n/a
29	chr3:42641690-42641740	NT2-D1	testis:	n/a
30	chr3:42641690-42641740	NHDF-neo	bronchial:	n/a
31	chr3:42641690-42641740	HCPEpiC	choroid plexus:	n/a
32	chr3:42641690-42641740	AG09309	skin:	n/a
33	chr3:42641690-42641740	MCF-7	breast:	n/a
34	chr3:42641690-42641740	IMR90	lung:	fetal
35	chr3:42641690-42641740	HCT-116	colon:	n/a
36	chr3:42641690-42641740	NHBE	bronchial:	n/a
37	chr3:42641690-42641740	ovcar-3	ovarian:	n/a
38	chr3:42641690-42641740	PrEC	prostate:	n/a
39	chr3:42641690-42641740	Jurkat	blood:	n/a
40	chr3:42641690-42641740	GM06990	blood:	n/a
41	chr3:42641690-42641740	PANC-1	pancreas:	n/a
42	chr3:42641690-42641740	ECC-1	luminal epithelium:	n/a
43	chr3:42641690-42641740	SK-N-MC	brain:	n/a
44	chr3:42641690-42641740	GM12891	blood:	n/a
45	chr3:42641690-42641740	Caco-2	colon:	n/a
46	chr3:42641690-42641740	HIPEpiC	eye:	n/a
47	chr3:42641690-42641740	SK-N-SH_RA	brain:	n/a
48	chr3:42641690-42641740	K562	blood:	n/a
49	chr3:42641690-42641740	AG04449	skin:	fetal
50	chr3:42641690-42641740	SK-N-SH	brain:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:42629943..42634676-chr3:42635408..42643782,10	MCF-7	breast:
2	chr19:58694266..58695104-chr3:42641451..42642305,2	Hela-S3	cervix:
3	chr15:85259297..85260034-chr3:42641537..42642490,2	Hela-S3	cervix:
4	chr17:62223147..62223727-chr3:42641596..42642594,2	Hela-S3	cervix:
5	chr3:42619900..42621497-chr3:42638395..42640003,2	MCF-7	breast:
6	chr3:42622208..42623993-chr3:42640628..42642693,2	MCF-7	breast:
7	chr3:42639395..42643636-chr3:42699754..42702498,4	K562	blood:
8	chr3:42640361..42643591-chr3:42693270..42696162,5	K562	blood:
9	chr3:42621283..42625330-chr3:42639303..42643596,7	MCF-7	breast:
10	chr3:42604560..42606277-chr3:42641170..42643967,2	K562	blood:
11	chr3:42641686..42642395-chr3:105587711..105588497,2	Hela-S3	cervix:
12	chr3:42640678..42643591-chr3:42694568..42696079,2	K562	blood:
13	chr3:42641420..42642298-chr8:144952427..144952949,2	HCT-116	colon:
14	chr3:42631664..42634178-chr3:42636385..42639345,6	MCF-7	breast:
15	chr3:42509273..42511295-chr3:42641295..42643446,2	MCF-7	breast:
16	chr2:85132538..85133319-chr3:42641468..42642648,3	Hela-S3	cervix:
17	chr3:42632553..42639930-chr3:42692933..42696882,8	K562	blood:
18	chr16:75589583..75590159-chr3:42641596..42642441,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
NKTR	TF binding region
NKTR	CpG island
ENSG00000171606	chromatin interactions
ENSG00000114423	chromatin interactions
ENSG00000008324	chromatin interactions
ENSG00000199753	chromatin interactions
ENSG00000114853	chromatin interactions
ENSG00000034510	chromatin interactions
ENSG00000227184	chromatin interactions
ENSG00000266402	chromatin interactions
ENSG00000230084	chromatin interactions
ENSG00000205084	chromatin interactions
ENSG00000235787	chromatin interactions
ENSG00000140612	chromatin interactions
ENSG00000093183	chromatin interactions

Extended variants
information (count: 93 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:93 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531653938	chr3:42638869-42638870	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs568392387	chr3:42638871-42638872	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs534184223	chr3:42638874-42638875	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs370995770	chr3:42638902-42638903	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs57411153	chr3:42638930-42638931	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs554211926	chr3:42638958-42638959	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs182587407	chr3:42639002-42639003	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs377425944	chr3:42639016-42639017	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs556758793	chr3:42639047-42639048	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs576224905	chr3:42639049-42639050	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs541587214	chr3:42639198-42639199	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs561804285	chr3:42639281-42639282	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs571985440	chr3:42639282-42639283	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs541018966	chr3:42639307-42639308	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs564043190	chr3:42639423-42639424	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs533018806	chr3:42639446-42639447	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs607568	chr3:42639452-42639453	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs568728289	chr3:42639506-42639507	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs563116000	chr3:42639513-42639514	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs536158124	chr3:42639552-42639553	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs187151145	chr3:42639585-42639586	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs548430993	chr3:42639775-42639776	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs192904755	chr3:42639786-42639787	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs533987200	chr3:42639799-42639800	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs183595693	chr3:42639807-42639808	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs199912002	chr3:42639827-42639828	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs374711277	chr3:42639828-42639829	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs547726455	chr3:42639850-42639851	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs533864032	chr3:42639867-42639868	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs571174336	chr3:42639877-42639878	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs374193888	chr3:42639881-42639882	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs540108001	chr3:42639882-42639883	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs558415250	chr3:42639883-42639884	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs138480981	chr3:42639933-42639934	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs576743617	chr3:42639960-42639961	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs536036639	chr3:42639962-42639963	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs149258621	chr3:42639976-42639977	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs557580230	chr3:42639979-42639980	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs572060267	chr3:42640043-42640044	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs540681155	chr3:42640124-42640125	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs557297555	chr3:42640135-42640136	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs78167645	chr3:42640225-42640226	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs543342136	chr3:42640227-42640228	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs563229086	chr3:42640274-42640275	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs188499306	chr3:42640296-42640297	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs138246973	chr3:42640316-42640317	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs113267661	chr3:42640329-42640330	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs562047774	chr3:42640332-42640333	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs527748476	chr3:42640354-42640355	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs77291243	chr3:42640385-42640386	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
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
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	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
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Wilms tumour	17204608	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-small cell lung cancer	21829676	CNVD
Kartagener syndrome	16639409	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Breast cancer	21509527	CNVD
Melanoma	21693616	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Breast cancer	20409316	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:312 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:42633200-42641400	Weak transcription	Aorta	Aorta
2	chr3:42633200-42641600	Weak transcription	Gastric	stomach
3	chr3:42633400-42641200	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr3:42633400-42641200	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr3:42633400-42641200	Weak transcription	HSMMtube	muscle
6	chr3:42633400-42641400	Weak transcription	Ovary	ovary
7	chr3:42633400-42641400	Weak transcription	Psoas Muscle	Psoas
8	chr3:42633400-42641400	Weak transcription	Right Ventricle	heart
9	chr3:42633400-42641600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr3:42633400-42641600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr3:42633400-42641600	Weak transcription	Esophagus	oesophagus
12	chr3:42633400-42641600	Weak transcription	Spleen	Spleen
13	chr3:42633600-42639200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr3:42633600-42639400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr3:42633600-42641200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr3:42633600-42641200	Weak transcription	Colon Smooth Muscle	Colon
17	chr3:42633600-42641200	Weak transcription	Fetal Kidney	kidney
18	chr3:42633600-42641200	Weak transcription	Rectal Smooth Muscle	rectum
19	chr3:42633600-42641200	Weak transcription	Right Atrium	heart
20	chr3:42633600-42641200	Weak transcription	NHEK	skin
21	chr3:42633600-42641400	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr3:42633600-42641400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr3:42633600-42641400	Weak transcription	Brain Anterior Caudate	brain
24	chr3:42633600-42641600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr3:42633600-42641600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr3:42633600-42641600	Weak transcription	Pancreas	Pancrea
27	chr3:42633800-42641200	Weak transcription	Brain Germinal Matrix	brain
28	chr3:42634000-42641200	Weak transcription	Fetal Intestine Small	intestine
29	chr3:42634000-42641600	Weak transcription	Lung	lung
30	chr3:42634400-42641200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
31	chr3:42634600-42641200	Weak transcription	Fetal Brain Male	brain
32	chr3:42635000-42639400	Strong transcription	HSMM	muscle
33	chr3:42635000-42639600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
34	chr3:42635400-42641200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
35	chr3:42635400-42641200	Weak transcription	Brain Angular Gyrus	brain
36	chr3:42635600-42640800	Weak transcription	Hela-S3	cervix
37	chr3:42635600-42641200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr3:42635600-42641200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr3:42635600-42641200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
40	chr3:42635600-42641200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr3:42635600-42641200	Weak transcription	Fetal Stomach	stomach
42	chr3:42635600-42641200	Weak transcription	Placenta Amnion	Placenta Amnion
43	chr3:42635600-42641400	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr3:42635600-42641600	Weak transcription	Small Intestine	intestine
45	chr3:42635800-42641200	Weak transcription	HepG2	liver
46	chr3:42636000-42641200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr3:42636000-42641200	Weak transcription	Brain Hippocampus Middle	brain
48	chr3:42636000-42641200	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr3:42636000-42641400	Weak transcription	Brain Cingulate Gyrus	brain
50	chr3:42636200-42641200	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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