Variant report

Variant	esv1824927
Chromosome Location	chr4:119521936-119577466
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:292)
CpG islands
(count:427)
Chromatin interactive
region (count:1)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:292 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr4:119546600-119546871	GM12878	blood:	n/a	n/a
2	BCL11A	chr4:119547576-119547749	GM12878	blood:	n/a	n/a
3	BHLHE40	chr4:119550987-119551186	K562	blood:	n/a	n/a
4	BHLHE40	chr4:119576461-119576486	HepG2	liver:	n/a	n/a
5	CBX3	chr4:119530825-119531192	K562	blood:	n/a	n/a
6	CBX3	chr4:119550881-119551228	K562	blood:	n/a	n/a
7	CEBPB	chr4:119550980-119551187	A549	lung:	n/a	n/a
8	CEBPB	chr4:119575027-119575397	K562	blood:	n/a	n/a
9	CEBPB	chr4:119550959-119551180	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr4:119544384-119544591	K562	blood:	n/a	n/a
11	CEBPB	chr4:119550798-119551230	IMR90	lung:	n/a	n/a
12	CEBPB	chr4:119550971-119551171	K562	blood:	n/a	n/a
13	CEBPB	chr4:119566666-119567031	K562	blood:	n/a	n/a
14	CEBPB	chr4:119563765-119563790	HepG2	liver:	n/a	chr4:119563768-119563779 chr4:119563767-119563780
15	CEBPB	chr4:119541445-119541681	K562	blood:	n/a	chr4:119541607-119541618
16	CEBPB	chr4:119550892-119551149	K562	blood:	n/a	n/a
17	CEBPD	chr4:119570052-119570409	K562	blood:	n/a	n/a
18	CEBPD	chr4:119574979-119575474	K562	blood:	n/a	n/a
19	CTCF	chr4:119550980-119551130	HBMEC	blood vessel:	n/a	n/a
20	CTCF	chr4:119571229-119571274	Pancreas_OC	pancreas:	n/a	n/a
21	CTCF	chr4:119550880-119551030	AG04449	skin:	n/a	n/a
22	CTCF	chr4:119575082-119575277	K562	blood:	n/a	chr4:119575211-119575232
23	CTCF	chr4:119550880-119551030	HPF	lung:	n/a	n/a
24	CTCF	chr4:119550928-119551068	Gliobla	brain:	n/a	n/a
25	CTCF	chr4:119550980-119551130	HCFaa	heart:	n/a	n/a
26	CTCF	chr4:119552227-119552364	MCF-7	breast:	n/a	chr4:119552304-119552317 chr4:119552305-119552315 chr4:119552302-119552320 chr4:119552297-119552318 chr4:119552308-119552317
27	CTCF	chr4:119550940-119551090	MCF-7	breast:	n/a	n/a
28	CTCF	chr4:119550560-119550710	HBMEC	blood vessel:	n/a	n/a
29	CTCF	chr4:119550900-119551050	AG04449	skin:	n/a	n/a
30	CTCF	chr4:119552212-119552370	MCF-7	breast:	n/a	chr4:119552304-119552317 chr4:119552305-119552315 chr4:119552302-119552320 chr4:119552297-119552318 chr4:119552308-119552317
31	CTCF	chr4:119550940-119551090	HRPEpiC	eye:	n/a	n/a
32	CTCF	chr4:119550900-119551050	HMEC	breast:	n/a	n/a
33	CTCF	chr4:119550980-119551130	AG10803	skin:	n/a	n/a
34	CTCF	chr4:119552340-119552490	WERI-Rb-1	eye:	n/a	chr4:119552363-119552376
35	CTCF	chr4:119552275-119552357	HepG2	liver:	n/a	chr4:119552304-119552317 chr4:119552305-119552315 chr4:119552302-119552320 chr4:119552297-119552318 chr4:119552308-119552317
36	CTCF	chr4:119550900-119551050	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr4:119550920-119551070	HAc	cerebellar:	n/a	n/a
38	CTCF	chr4:119550900-119551050	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr4:119552286-119552345	MCF-7	breast:	n/a	chr4:119552304-119552317 chr4:119552305-119552315 chr4:119552302-119552320 chr4:119552297-119552318 chr4:119552308-119552317
40	CTCF	chr4:119554627-119554944	K562	blood:	n/a	n/a
41	CTCF	chr4:119550980-119551130	SAEC	small airway:	n/a	n/a
42	CTCF	chr4:119551865-119552362	K562	blood:	n/a	chr4:119552304-119552317 chr4:119552305-119552315 chr4:119552043-119552061 chr4:119552302-119552320 chr4:119552297-119552318 chr4:119552308-119552317
43	CTCF	chr4:119550940-119551090	AG04450	lung:	n/a	n/a
44	CTCF	chr4:119552018-119552130	K562	blood:	n/a	chr4:119552043-119552061
45	CTCF	chr4:119550880-119551030	AoAF	blood vessel:	n/a	n/a
46	CTCF	chr4:119550940-119551090	HCT-116	colon:	n/a	n/a
47	CTCF	chr4:119550980-119551130	HMF	breast:	n/a	n/a
48	CTCF	chr4:119550974-119551031	Fibrobl	skin:	n/a	n/a
49	CTCF	chr4:119550933-119551054	NHEK	skin:	n/a	n/a
50	CTCF	chr4:119550940-119551090	HFF-Myc	foreskin:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:119554219-119554269	NB4	blood:	n/a
2	chr4:119553015-119553065	AG04449	skin:	fetal
3	chr4:119554219-119554269	BE2_C	brain:	n/a
4	chr4:119556601-119556651	GM12891	blood:	n/a
5	chr4:119553015-119553065	CMK	blood:	n/a
6	chr4:119553015-119553065	SK-N-SH_RA	brain:	n/a
7	chr4:119556601-119556651	HAEpiC	amniotic membrane:	n/a
8	chr4:119553015-119553065	HEK293	kidney:	embryo
9	chr4:119557464-119557514	HRCEpiC	kidney:	n/a
10	chr4:119553015-119553065	HL-60	blood:	n/a
11	chr4:119557464-119557514	HUVEC	blood vessel:	n/a
12	chr4:119556601-119556651	AoSMC	blood vessel:	n/a
13	chr4:119557464-119557514	AG09319	gingival:	n/a
14	chr4:119556601-119556651	HL-60	blood:	n/a
15	chr4:119553015-119553065	H1-hESC	embryonic stem cell:	embryo
16	chr4:119554219-119554269	SK-N-SH_RA	brain:	n/a
17	chr4:119556601-119556651	BE2_C	brain:	n/a
18	chr4:119550632-119550682	ovcar-3	ovarian:	n/a
19	chr4:119555395-119555445	SK-N-MC	brain:	n/a
20	chr4:119555556-119555606	SK-N-MC	brain:	n/a
21	chr4:119557464-119557514	MCF-7	breast:	n/a
22	chr4:119557464-119557514	RPTEC	kidney:	n/a
23	chr4:119553015-119553065	LNCaP	prostate:	n/a
24	chr4:119550632-119550682	A549	lung:	n/a
25	chr4:119557464-119557514	AG10803	skin:	n/a
26	chr4:119554219-119554269	T-47D	breast:	n/a
27	chr4:119555395-119555445	HRE	kidney:	n/a
28	chr4:119554219-119554269	HPAEpiC	pulmonary alveolar:	n/a
29	chr4:119550632-119550682	HL-60	blood:	n/a
30	chr4:119554219-119554269	Jurkat	blood:	n/a
31	chr4:119553015-119553065	AoSMC	blood vessel:	n/a
32	chr4:119557464-119557514	AoSMC	blood vessel:	n/a
33	chr4:119555395-119555445	GM06990	blood:	n/a
34	chr4:119557464-119557514	AG04450	lung:	fetal
35	chr4:119556601-119556651	HPAEpiC	pulmonary alveolar:	n/a
36	chr4:119557464-119557514	ECC-1	luminal epithelium:	n/a
37	chr4:119557464-119557514	BE2_C	brain:	n/a
38	chr4:119550632-119550682	Caco-2	colon:	n/a
39	chr4:119555556-119555606	GM12878	blood:	n/a
40	chr4:119555556-119555606	BE2_C	brain:	n/a
41	chr4:119556601-119556651	CMK	blood:	n/a
42	chr4:119554219-119554269	SK-N-SH	brain:	n/a
43	chr4:119555395-119555445	HNPCEpiC	eye:	n/a
44	chr4:119550632-119550682	H1-hESC	embryonic stem cell:	embryo
45	chr4:119555556-119555606	ECC-1	luminal epithelium:	n/a
46	chr4:119554219-119554269	HepG2	liver:	n/a
47	chr4:119555395-119555445	HIPEpiC	eye:	n/a
48	chr4:119553015-119553065	SK-N-MC	brain:	n/a
49	chr4:119554219-119554269	NH-A	brain:	n/a
50	chr4:119555556-119555606	AG09319	gingival:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:119200131..119202202-chr4:119563480..119565428,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-METTL14-2	chr4:119532090-119532293	FPKM1_group_23959_transcript_1
2	lnc-METTL14-1	chr4:119541986-119541991	NONHSAT097989
3	lnc-METTL14-2	chr4:119532091-119532293	XLOC_003662
4	lnc-METTL14-2	chr4:119539320-119539356	NONHSAT097987
5	lnc-METTL14-1	chr4:119541987-119541991	XLOC_003663
6	lnc-METTL14-2	chr4:119539321-119539356	XLOC_003662
7	lnc-METTL14-2	chr4:119532090-119532293	NONHSAT097987
8	lnc-METTL14-1	chr4:119541480-119541765	XLOC_003663
9	lnc-METTL14-2	chr4:119532813-119532849	FPKM1_group_23959_transcript_1
10	lnc-METTL14-1	chr4:119541479-119541765	NONHSAT097989

No data

Variant related genes	Relation type
ENSG00000251155	TF binding region
CICP16	TF binding region
ENSG00000225892	TF binding region
RNU6-1054P	TF binding region
ENSG00000251155	CpG island
CICP16	CpG island
ENSG00000225892	CpG island
RNU6-1054P	CpG island
ENSG00000269893	chromatin interactions
PPM1D	miRNA target sites

Extended variants
information (count: 1315 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:1315 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372016922	chr4:119521977-119521978	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs376950912	chr4:119521979-119521980	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs528567038	chr4:119521981-119521982	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548572343	chr4:119521997-119521998	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs147872820	chr4:119522096-119522097	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs530609189	chr4:119522148-119522149	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs369412777	chr4:119522157-119522158	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs570791290	chr4:119522195-119522196	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs200035835	chr4:119522218-119522219	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs139915264	chr4:119522221-119522222	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs572147887	chr4:119522225-119522226	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs373167115	chr4:119522235-119522236	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534383146	chr4:119522270-119522271	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs554610417	chr4:119522339-119522340	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs183813107	chr4:119522380-119522381	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201764153	chr4:119522389-119522390	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs543756360	chr4:119522405-119522406	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs62326242	chr4:119522418-119522419	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs577189330	chr4:119522424-119522425	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187046963	chr4:119522458-119522459	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs375674027	chr4:119522506-119522507	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs546018276	chr4:119522524-119522525	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs370294263	chr4:119522582-119522583	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs372693506	chr4:119522604-119522605	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528589539	chr4:119522616-119522617	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201903881	chr4:119522648-119522649	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371030611	chr4:119522675-119522676	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs191949433	chr4:119522687-119522688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544859888	chr4:119522690-119522691	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561759731	chr4:119522835-119522836	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560960658	chr4:119522878-119522879	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs375201058	chr4:119522879-119522880	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs185376060	chr4:119522887-119522888	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs530845282	chr4:119522922-119522923	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190307704	chr4:119523018-119523019	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570859414	chr4:119523061-119523062	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539737524	chr4:119523075-119523076	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs143128218	chr4:119523079-119523080	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547184634	chr4:119523094-119523095	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs566907585	chr4:119523183-119523184	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs534739238	chr4:119523252-119523253	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554671948	chr4:119523253-119523254	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs574570244	chr4:119523255-119523256	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537073690	chr4:119523266-119523267	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556985354	chr4:119523278-119523279	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs182542536	chr4:119523283-119523284	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545732888	chr4:119523301-119523302	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559520514	chr4:119523337-119523338	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs546650762	chr4:119523348-119523349	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374346241	chr4:119523354-119523355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Autism	19246517	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD

Chromatin state (count:413 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:119513400-119522800	Weak transcription	Small Intestine	intestine
2	chr4:119513400-119527800	Weak transcription	Brain Substantia Nigra	brain
3	chr4:119513400-119528200	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr4:119513400-119528400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr4:119513400-119534800	Weak transcription	Primary B cells from cord blood	blood
6	chr4:119513400-119551400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr4:119513400-119554000	Weak transcription	Colon Smooth Muscle	Colon
8	chr4:119513400-119554800	Weak transcription	Ovary	ovary
9	chr4:119513400-119557200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr4:119513600-119522200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr4:119513600-119524000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr4:119513600-119526400	Weak transcription	Left Ventricle	heart
13	chr4:119513600-119526600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr4:119513600-119526600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr4:119513600-119526600	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr4:119513600-119526800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr4:119513600-119527000	Weak transcription	Primary B cells from peripheral blood	blood
18	chr4:119513600-119527200	Weak transcription	Brain Germinal Matrix	brain
19	chr4:119513600-119528000	Weak transcription	HSMMtube	muscle
20	chr4:119513600-119529000	Weak transcription	Brain Cingulate Gyrus	brain
21	chr4:119513600-119530600	Weak transcription	Primary T cells from cord blood	blood
22	chr4:119513600-119536800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr4:119513600-119539200	Weak transcription	Primary hematopoietic stem cells	blood
24	chr4:119513600-119549200	Weak transcription	Esophagus	oesophagus
25	chr4:119513600-119550400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr4:119513600-119551000	Weak transcription	Pancreas	Pancrea
27	chr4:119513600-119551600	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr4:119513600-119552400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr4:119513600-119552400	Weak transcription	Primary T helper cells PMA-I stimulated	--
30	chr4:119513600-119552400	Weak transcription	Fetal Brain Female	brain
31	chr4:119513600-119552400	Weak transcription	Lung	lung
32	chr4:119513600-119552400	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr4:119513600-119554000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr4:119513600-119555800	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr4:119513600-119559200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr4:119513800-119526600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr4:119513800-119526800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr4:119513800-119527400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr4:119513800-119551200	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr4:119513800-119552400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr4:119513800-119555000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr4:119513800-119556000	Weak transcription	Fetal Lung	lung
43	chr4:119517400-119526200	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr4:119518000-119523000	Strong transcription	Fetal Stomach	stomach
45	chr4:119518200-119522600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr4:119518200-119523600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr4:119518400-119552600	Weak transcription	H9 Cell Line	embryonic stem cell
48	chr4:119518800-119557000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr4:119519000-119526400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr4:119519000-119526600	Weak transcription	Sigmoid Colon	Sigmoid Colon

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links