Variant report

Variant	nsv822432
Chromosome Location	chr4:1225517-1226594
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:31)
CpG islands
(count:183)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:31 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr4:1225798-1225948	HepG2	liver:	n/a	n/a
2	EP300	chr4:1226388-1227661	SK-N-SH	brain:	n/a	n/a
3	FOSL2	chr4:1225711-1226051	HepG2	liver:	n/a	n/a
4	HNF4A	chr4:1225792-1226047	HepG2	liver:	n/a	n/a
5	JUND	chr4:1225857-1226007	HepG2	liver:	n/a	n/a
6	MXI1	chr4:1226347-1228997	SK-N-SH	brain:	n/a	chr4:1227056-1227071 chr4:1227020-1227035
7	NR2F2	chr4:1225714-1226179	HepG2	liver:	n/a	n/a
8	POLR2A	chr4:1225869-1226034	K562	blood:	n/a	n/a
9	POLR2A	chr4:1225621-1225627	GM12878	blood:	n/a	n/a
10	POLR2A	chr4:1224742-1226033	K562	blood:	n/a	n/a
11	POLR2A	chr4:1225487-1225518	H1-hESC	embryonic stem cell:	n/a	n/a
12	POLR2A	chr4:1225378-1225570	A549	lung:	n/a	n/a
13	POLR2A	chr4:1225575-1225736	GM12878	blood:	n/a	n/a
14	POLR2A	chr4:1225430-1225655	IMR90	lung:	n/a	n/a
15	POLR2A	chr4:1226522-1227240	GM12892	blood:	n/a	n/a
16	POLR2A	chr4:1225114-1225732	SK-N-MC	brain:	n/a	n/a
17	POLR2A	chr4:1226591-1226754	K562	blood:	n/a	n/a
18	POLR2A	chr4:1226483-1226722	ECC-1	luminal epithelium:	n/a	n/a
19	POLR2A	chr4:1225424-1225959	HepG2	liver:	n/a	n/a
20	POLR2A	chr4:1225352-1225533	K562	blood:	n/a	n/a
21	POLR2A	chr4:1226299-1226584	HepG2	liver:	n/a	n/a
22	POLR2A	chr4:1225511-1225584	K562	blood:	n/a	n/a
23	POLR2A	chr4:1226166-1226250	K562	blood:	n/a	n/a
24	POLR2A	chr4:1225309-1225614	ECC-1	luminal epithelium:	n/a	n/a
25	POLR2A	chr4:1225471-1225667	K562	blood:	n/a	n/a
26	POLR2A	chr4:1226588-1226918	GM12878	blood:	n/a	n/a
27	POLR2A	chr4:1226092-1226309	K562	blood:	n/a	n/a
28	POLR2A	chr4:1226260-1226265	K562	blood:	n/a	n/a
29	POLR2A	chr4:1226546-1226826	HepG2	liver:	n/a	n/a
30	POLR2A	chr4:1226456-1228347	K562	blood:	n/a	n/a
31	POLR2A	chr4:1224823-1225730	HepG2	liver:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:1225729-1225779	H1-hESC	embryonic stem cell:	embryo
2	chr4:1225729-1225779	SK-N-SH_RA	brain:	n/a
3	chr4:1225729-1225779	AG09309	skin:	n/a
4	chr4:1225729-1225779	PANC-1	pancreas:	n/a
5	chr4:1225729-1225779	SKMC	muscle:	n/a
6	chr4:1225599-1225649	HCT-116	colon:	n/a
7	chr4:1225507-1225557	PANC-1	pancreas:	n/a
8	chr4:1225507-1225557	ProgFib	skin:	n/a
9	chr4:1225507-1225557	Hela-S3	cervix:	n/a
10	chr4:1225729-1225779	HPAEpiC	pulmonary alveolar:	n/a
11	chr4:1225729-1225779	PrEC	prostate:	n/a
12	chr4:1225599-1225649	U87	brain:	n/a
13	chr4:1225507-1225557	MCF-7	breast:	n/a
14	chr4:1225507-1225557	SKMC	muscle:	n/a
15	chr4:1225599-1225649	MCF10A-Er-Src	breast:	n/a
16	chr4:1225507-1225557	SK-N-SH	brain:	n/a
17	chr4:1225729-1225779	ovcar-3	ovarian:	n/a
18	chr4:1225729-1225779	ECC-1	luminal epithelium:	n/a
19	chr4:1225507-1225557	HIPEpiC	eye:	n/a
20	chr4:1225599-1225649	PrEC	prostate:	n/a
21	chr4:1225599-1225649	AG04449	skin:	fetal
22	chr4:1225507-1225557	NB4	blood:	n/a
23	chr4:1225507-1225557	BJ	skin:	n/a
24	chr4:1225599-1225649	MCF-7	breast:	n/a
25	chr4:1225729-1225779	T-47D	breast:	n/a
26	chr4:1225729-1225779	AG04449	skin:	fetal
27	chr4:1225729-1225779	HNPCEpiC	eye:	n/a
28	chr4:1225599-1225649	GM12878	blood:	n/a
29	chr4:1225599-1225649	GM19239	blood:	n/a
30	chr4:1225507-1225557	MCF10A-Er-Src	breast:	n/a
31	chr4:1225507-1225557	SAEC	small airway:	n/a
32	chr4:1225599-1225649	SK-N-MC	brain:	n/a
33	chr4:1225507-1225557	A549	lung:	n/a
34	chr4:1225507-1225557	IMR90	lung:	fetal
35	chr4:1225599-1225649	HIPEpiC	eye:	n/a
36	chr4:1225599-1225649	T-47D	breast:	n/a
37	chr4:1225729-1225779	Jurkat	blood:	n/a
38	chr4:1225729-1225779	HRPEpiC	eye:	n/a
39	chr4:1225507-1225557	GM12891	blood:	n/a
40	chr4:1225599-1225649	ECC-1	luminal epithelium:	n/a
41	chr4:1225729-1225779	NB4	blood:	n/a
42	chr4:1225729-1225779	HCM	heart:	n/a
43	chr4:1225599-1225649	Caco-2	colon:	n/a
44	chr4:1225599-1225649	HepG2	liver:	n/a
45	chr4:1225729-1225779	BJ	skin:	n/a
46	chr4:1225599-1225649	RPTEC	kidney:	n/a
47	chr4:1225507-1225557	K562	blood:	n/a
48	chr4:1225599-1225649	H1-hESC	embryonic stem cell:	embryo
49	chr4:1225507-1225557	HRE	kidney:	n/a
50	chr4:1225729-1225779	HCPEpiC	choroid plexus:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:1205834..1208746-chr4:1226457..1228401,2	K562	blood:
2	chr4:1221651..1224397-chr4:1224479..1227066,2	MCF-7	breast:
3	chr4:1159882..1162594-chr4:1225934..1228487,2	MCF-7	breast:
4	chr4:1219143..1221497-chr4:1224349..1226849,2	MCF-7	breast:

No data

Variant related genes	Relation type
CTBP1	TF binding region
CTBP1	CpG island
ENSG00000159692	chromatin interactions
ENSG00000273179	chromatin interactions

Extended variants
information (count: 62 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:62 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528711995	chr4:1225553-1225554	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs3822018	chr4:1225554-1225555	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs189591696	chr4:1225578-1225579	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs150857386	chr4:1225599-1225600	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs113911972	chr4:1225662-1225663	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs536391950	chr4:1225672-1225673	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs376665974	chr4:1225696-1225697	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs59780026	chr4:1225697-1225698	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs541721262	chr4:1225703-1225704	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs553672705	chr4:1225717-1225718	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs1250112	chr4:1225723-1225724	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs545580694	chr4:1225733-1225734	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs569008791	chr4:1225750-1225751	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs563912285	chr4:1225751-1225752	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs56007462	chr4:1225775-1225776	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs543150910	chr4:1225783-1225784	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs1250111	chr4:1225795-1225796	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs192629055	chr4:1225820-1225821	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs146559107	chr4:1225824-1225825	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs571175589	chr4:1225846-1225847	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs114377282	chr4:1225877-1225878	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs370224718	chr4:1225880-1225881	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs534530163	chr4:1225912-1225913	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs550498055	chr4:1225926-1225927	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs184415257	chr4:1225950-1225951	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs190574111	chr4:1225981-1225982	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs546532201	chr4:1226012-1226013	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs566591122	chr4:1226050-1226051	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs182009357	chr4:1226053-1226054	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs558593536	chr4:1226061-1226062	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs578238770	chr4:1226091-1226092	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs77352542	chr4:1226093-1226094	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs200695965	chr4:1226097-1226098	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs376394171	chr4:1226118-1226119	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs575831263	chr4:1226131-1226132	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs554960949	chr4:1226138-1226139	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs542734411	chr4:1226148-1226149	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs34046906	chr4:1226170-1226171	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs561406030	chr4:1226244-1226245	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs186055267	chr4:1226258-1226259	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs540195823	chr4:1226271-1226272	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs564984825	chr4:1226280-1226281	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs188909824	chr4:1226291-1226292	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs532263666	chr4:1226310-1226311	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs141214540	chr4:1226342-1226343	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs568934485	chr4:1226347-1226348	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs34551351	chr4:1226358-1226359	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs529866633	chr4:1226379-1226380	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs1732132	chr4:1226384-1226385	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs1680048	chr4:1226385-1226386	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17142309	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	20932292	CNVD
Pancreatic cancer	17952125	CNVD
Type 2 diabetes	21754918	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20393555	CNVD

Chromatin state (count:158 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:1204400-1227200	Strong transcription	Fetal Intestine Small	intestine
2	chr4:1204400-1235800	Strong transcription	HUES6 Cell Line	embryonic stem cell
3	chr4:1204600-1236200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr4:1204800-1226400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr4:1204800-1237000	Weak transcription	Psoas Muscle	Psoas
6	chr4:1205000-1226200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr4:1205400-1226800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr4:1205800-1228200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr4:1206000-1226800	Strong transcription	Fetal Brain Female	brain
10	chr4:1206400-1226800	Strong transcription	Brain Germinal Matrix	brain
11	chr4:1206600-1227600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
12	chr4:1208800-1228000	Strong transcription	Muscle Satellite Cultured Cells	--
13	chr4:1211400-1235400	Weak transcription	Small Intestine	intestine
14	chr4:1211600-1235400	Strong transcription	Sigmoid Colon	Sigmoid Colon
15	chr4:1212600-1237000	Strong transcription	Dnd41	blood
16	chr4:1214200-1235600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr4:1214200-1236800	Strong transcription	Primary T cells from cord blood	blood
18	chr4:1214400-1225600	Strong transcription	Aorta	Aorta
19	chr4:1214400-1235200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr4:1214400-1235600	Strong transcription	H1 Cell Line	embryonic stem cell
21	chr4:1214400-1236400	Strong transcription	Primary neutrophils fromperipheralblood	blood
22	chr4:1214400-1238400	Strong transcription	Thymus	Thymus
23	chr4:1214600-1226400	Strong transcription	Cortex derived primary cultured neurospheres	brain
24	chr4:1214600-1227400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr4:1214600-1227600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr4:1214600-1235800	Strong transcription	Primary T helper cells fromperipheralblood	blood
27	chr4:1214600-1236200	Strong transcription	Monocytes-CD14+_RO01746	blood
28	chr4:1215000-1226800	Strong transcription	Colonic Mucosa	Colon
29	chr4:1215000-1235200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr4:1215000-1236000	Strong transcription	Primary monocytes fromperipheralblood	blood
31	chr4:1215400-1225800	Strong transcription	Brain Anterior Caudate	brain
32	chr4:1215400-1226600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr4:1215400-1236000	Strong transcription	Primary B cells from peripheral blood	blood
34	chr4:1215800-1226600	Strong transcription	Fetal Stomach	stomach
35	chr4:1215800-1235600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr4:1216400-1227800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr4:1216400-1227800	Strong transcription	Rectal Mucosa Donor 31	rectum
38	chr4:1216400-1235400	Strong transcription	Primary T helper cells PMA-I stimulated	--
39	chr4:1216400-1236000	Strong transcription	Fetal Thymus	thymus
40	chr4:1216600-1227200	Strong transcription	Placenta Amnion	Placenta Amnion
41	chr4:1216600-1236000	Strong transcription	GM12878-XiMat	blood
42	chr4:1216800-1225800	Strong transcription	Duodenum Smooth Muscle	Duodenum
43	chr4:1217000-1226800	Strong transcription	Duodenum Mucosa	Duodenum
44	chr4:1217000-1226800	Strong transcription	Rectal Mucosa Donor 29	rectum
45	chr4:1217200-1235400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
46	chr4:1217200-1235800	Strong transcription	iPS-15b Cell Line	embryonic stem cell
47	chr4:1217600-1235200	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr4:1217800-1225600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr4:1218200-1234600	Strong transcription	Primary T cells fromperipheralblood	blood
50	chr4:1218400-1226400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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