Variant report

Variant	nsv980265
Chromosome Location	chr4:147444399-147454944
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:54)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:54 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:147444301-147444570	K562	blood:	n/a	n/a
2	ATF1	chr4:147446984-147447324	K562	blood:	n/a	n/a
3	BHLHE40	chr4:147447001-147447424	K562	blood:	n/a	n/a
4	CEBPB	chr4:147445522-147445770	HepG2	liver:	n/a	chr4:147445600-147445611
5	CEBPB	chr4:147445498-147445732	A549	lung:	n/a	chr4:147445600-147445611
6	CTCF	chr4:147451533-147451599	GM10266	blood:	n/a	n/a
7	CTCF	chr4:147447709-147447734	Spleen_OC	spleen:	n/a	n/a
8	CTCF	chr4:147448800-147448950	HRE	kidney:	n/a	n/a
9	CUX1	chr4:147444071-147444414	K562	blood:	n/a	n/a
10	EBF1	chr4:147447069-147447388	GM12878	blood:	n/a	n/a
11	EGR1	chr4:147447197-147447425	K562	blood:	n/a	n/a
12	EP300	chr4:147446949-147447330	K562	blood:	n/a	chr4:147447193-147447207 chr4:147447194-147447203
13	EP300	chr4:147445301-147445432	K562	blood:	n/a	n/a
14	GATA3	chr4:147444375-147444666	SH-SY5Y	brain:	n/a	chr4:147444406-147444416
15	JUND	chr4:147447049-147447318	K562	blood:	n/a	n/a
16	MAFK	chr4:147442031-147444438	GM12878	blood:	n/a	chr4:147443552-147443569 chr4:147443430-147443440
17	MAX	chr4:147447158-147447345	K562	blood:	n/a	n/a
18	MAX	chr4:147447173-147447515	K562	blood:	n/a	n/a
19	MAX	chr4:147447232-147447386	K562	blood:	n/a	n/a
20	MYC	chr4:147447117-147447314	K562	blood:	n/a	n/a
21	NR2F2	chr4:147447050-147447410	K562	blood:	n/a	n/a
22	NR2F2	chr4:147441899-147444400	K562	blood:	n/a	n/a
23	PAX5	chr4:147450277-147450461	GM12878	blood:	n/a	n/a
24	PAX5	chr4:147450195-147450483	GM12878	blood:	n/a	n/a
25	PAX5	chr4:147450172-147450592	GM12878	blood:	n/a	n/a
26	PAX5	chr4:147450284-147450435	GM12878	blood:	n/a	n/a
27	POLR2A	chr4:147441877-147444739	GM12878	blood:	n/a	n/a
28	POLR2A	chr4:147446310-147448080	K562	blood:	n/a	n/a
29	POLR2A	chr4:147441905-147444891	IMR90	lung:	n/a	n/a
30	POLR2A	chr4:147441932-147444515	GM12878	blood:	n/a	n/a
31	POLR2A	chr4:147441951-147444453	K562	blood:	n/a	n/a
32	POLR2A	chr4:147445613-147445645	MCF10A-Er-Src	breast:	n/a	n/a
33	POLR2A	chr4:147444948-147446026	K562	blood:	n/a	n/a
34	POLR2A	chr4:147445389-147445832	MCF10A-Er-Src	breast:	n/a	n/a
35	POLR2A	chr4:147443490-147444616	K562	blood:	n/a	n/a
36	RCOR1	chr4:147446911-147447276	K562	blood:	n/a	n/a
37	RFX5	chr4:147444010-147444414	Hela-S3	cervix:	n/a	n/a
38	SPI1	chr4:147452725-147452910	K562	blood:	n/a	n/a
39	SPI1	chr4:147452725-147452932	K562	blood:	n/a	n/a
40	STAT3	chr4:147445524-147445649	MCF10A-Er-Src	breast:	n/a	n/a
41	STAT3	chr4:147444250-147444450	MCF10A-Er-Src	breast:	n/a	n/a
42	STAT3	chr4:147454938-147454979	MCF10A-Er-Src	breast:	n/a	n/a
43	TAF1	chr4:147447346-147447536	GM12892	blood:	n/a	n/a
44	TAL1	chr4:147447107-147447253	K562	blood:	n/a	chr4:147447240-147447251 chr4:147447242-147447253
45	TBL1XR1	chr4:147444064-147444494	K562	blood:	n/a	n/a
46	TCF12	chr4:147447172-147447359	GM12878	blood:	n/a	chr4:147447240-147447250
47	TCF12	chr4:147450302-147450498	GM12878	blood:	n/a	n/a
48	TCF3	chr4:147450280-147450472	GM12878	blood:	n/a	n/a
49	TEAD4	chr4:147446885-147447385	K562	blood:	n/a	n/a
50	USF1	chr4:147448589-147448760	HepG2	liver:	n/a	chr4:147448700-147448711

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:147448047-147448097	ECC-1	luminal epithelium:	n/a
2	chr4:147448047-147448097	GM06990	blood:	n/a
3	chr4:147448047-147448097	HCF	heart:	n/a
4	chr4:147448047-147448097	AG04449	skin:	fetal
5	chr4:147448047-147448097	HNPCEpiC	eye:	n/a
6	chr4:147448047-147448097	GM19239	blood:	n/a
7	chr4:147448047-147448097	MCF10A-Er-Src	breast:	n/a
8	chr4:147448047-147448097	HRCEpiC	kidney:	n/a
9	chr4:147448047-147448097	MCF-7	breast:	n/a
10	chr4:147448047-147448097	U87	brain:	n/a
11	chr4:147448047-147448097	A549	lung:	n/a
12	chr4:147448047-147448097	SAEC	small airway:	n/a
13	chr4:147448047-147448097	BJ	skin:	n/a
14	chr4:147448047-147448097	NH-A	brain:	n/a
15	chr4:147448047-147448097	IMR90	lung:	fetal
16	chr4:147448047-147448097	HPAEpiC	pulmonary alveolar:	n/a
17	chr4:147448047-147448097	HCT-116	colon:	n/a
18	chr4:147448047-147448097	GM12892	blood:	n/a
19	chr4:147448047-147448097	BE2_C	brain:	n/a
20	chr4:147448047-147448097	HIPEpiC	eye:	n/a
21	chr4:147448047-147448097	HAEpiC	amniotic membrane:	n/a
22	chr4:147448047-147448097	SK-N-SH_RA	brain:	n/a
23	chr4:147448047-147448097	ProgFib	skin:	n/a
24	chr4:147448047-147448097	HL-60	blood:	n/a
25	chr4:147448047-147448097	AG09309	skin:	n/a
26	chr4:147448047-147448097	AG10803	skin:	n/a
27	chr4:147448047-147448097	SK-N-SH	brain:	n/a
28	chr4:147448047-147448097	NHBE	bronchial:	n/a
29	chr4:147448047-147448097	HEK293	kidney:	embryo
30	chr4:147448047-147448097	HepG2	liver:	n/a
31	chr4:147448047-147448097	SKMC	muscle:	n/a
32	chr4:147448047-147448097	NT2-D1	testis:	n/a
33	chr4:147448047-147448097	GM12878	blood:	n/a
34	chr4:147448047-147448097	HRPEpiC	eye:	n/a
35	chr4:147448047-147448097	PFSK-1	brain:	n/a
36	chr4:147448047-147448097	K562	blood:	n/a
37	chr4:147448047-147448097	ovcar-3	ovarian:	n/a
38	chr4:147448047-147448097	T-47D	breast:	n/a
39	chr4:147448047-147448097	GM12891	blood:	n/a
40	chr4:147448047-147448097	Caco-2	colon:	n/a
41	chr4:147448047-147448097	PrEC	prostate:	n/a
42	chr4:147448047-147448097	HRE	kidney:	n/a
43	chr4:147448047-147448097	AG09319	gingival:	n/a
44	chr4:147448047-147448097	Hepatocyte	liver:	n/a
45	chr4:147448047-147448097	CMK	blood:	n/a
46	chr4:147448047-147448097	NB4	blood:	n/a
47	chr4:147448047-147448097	Hela-S3	cervix:	n/a
48	chr4:147448047-147448097	SK-N-MC	brain:	n/a
49	chr4:147448047-147448097	AoSMC	blood vessel:	n/a
50	chr4:147448047-147448097	NHDF-neo	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:147440616..147443246-chr4:147445900..147447774,2	MCF-7	breast:
2	chr4:147438639..147441130-chr4:147443226..147445590,2	MCF-7	breast:
3	chr4:147444230..147446047-chr4:147464429..147467416,2	K562	blood:
4	chr4:147429465..147431339-chr4:147443372..147446035,2	MCF-7	breast:

No data

Variant related genes	Relation type
SLC10A7	TF binding region
SLC10A7	CpG island
ENSG00000120519	chromatin interactions

Extended variants
information (count: 262 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:262 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190897523	chr4:147444402-147444403	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs546378649	chr4:147444436-147444437	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs149376851	chr4:147444456-147444457	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs182448196	chr4:147444504-147444505	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs186143520	chr4:147444581-147444582	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs561921499	chr4:147444582-147444583	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs112141216	chr4:147444594-147444595	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs530903746	chr4:147444645-147444646	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs550686526	chr4:147444648-147444649	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs540566608	chr4:147444697-147444698	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs144709081	chr4:147444808-147444809	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs532212437	chr4:147444929-147444930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs9994455	chr4:147444938-147444939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs148537344	chr4:147444950-147444951	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs527776736	chr4:147444958-147444959	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs553926246	chr4:147444961-147444962	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs565990704	chr4:147444999-147445000	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs534596587	chr4:147445000-147445001	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs142728673	chr4:147445088-147445089	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs567985926	chr4:147445093-147445094	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs537004817	chr4:147445146-147445147	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs75067507	chr4:147445201-147445202	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs552122354	chr4:147445246-147445247	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs577003325	chr4:147445261-147445262	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs540086196	chr4:147445284-147445285	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs553585450	chr4:147445349-147445350	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs73852879	chr4:147445367-147445368	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs35559029	chr4:147445386-147445387	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs34213717	chr4:147445503-147445504	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs532459506	chr4:147445526-147445527	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs575555815	chr4:147445568-147445569	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs544188740	chr4:147445569-147445570	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs564285217	chr4:147445580-147445581	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs550860139	chr4:147445620-147445621	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs146066618	chr4:147445629-147445630	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs78573563	chr4:147445630-147445631	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs559298701	chr4:147445633-147445634	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs529745260	chr4:147445638-147445639	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs528261573	chr4:147445639-147445640	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs183182963	chr4:147445679-147445680	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs141756331	chr4:147445682-147445683	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs114149493	chr4:147445817-147445818	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs369057162	chr4:147445869-147445870	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs187336720	chr4:147445883-147445884	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs550592984	chr4:147445942-147445943	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs570590990	chr4:147445969-147445970	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs566600948	chr4:147445975-147445976	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs539527018	chr4:147445979-147445980	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs553071180	chr4:147445986-147445987	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs371985223	chr4:147446008-147446009	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Intellectual disability	22102821	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
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	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
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	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
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21633010	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:160 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:147439200-147444400	Active TSS	GM12878-XiMat	blood
2	chr4:147441000-147444400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr4:147441000-147444400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr4:147441000-147444400	Active TSS	Right Atrium	heart
5	chr4:147441000-147444600	Active TSS	Fetal Brain Female	brain
6	chr4:147441400-147444400	Active TSS	HMEC	breast
7	chr4:147441400-147444400	Active TSS	NHDF-Ad	bronchial
8	chr4:147441800-147444400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr4:147441800-147444400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr4:147441800-147444400	Active TSS	Right Ventricle	heart
11	chr4:147441800-147444600	Active TSS	Muscle Satellite Cultured Cells	--
12	chr4:147442000-147444400	Active TSS	Breast Myoepithelial Primary Cells	Breast
13	chr4:147442000-147444400	Active TSS	Fetal Intestine Small	intestine
14	chr4:147442000-147444400	Active TSS	Fetal Muscle Trunk	muscle
15	chr4:147442000-147444400	Active TSS	Placenta	Placenta
16	chr4:147442000-147444400	Active TSS	Fetal Thymus	thymus
17	chr4:147442000-147444400	Active TSS	Rectal Smooth Muscle	rectum
18	chr4:147442000-147444400	Active TSS	Stomach Smooth Muscle	stomach
19	chr4:147442000-147444600	Active TSS	Pancreatic Islets	Pancreatic Islet
20	chr4:147442000-147444600	Active TSS	Thymus	Thymus
21	chr4:147442200-147444400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
22	chr4:147442200-147444400	Active TSS	Duodenum Smooth Muscle	Duodenum
23	chr4:147442200-147444400	Active TSS	Fetal Intestine Large	intestine
24	chr4:147442200-147444400	Active TSS	Fetal Kidney	kidney
25	chr4:147442200-147444400	Active TSS	Fetal Stomach	stomach
26	chr4:147442200-147444400	Active TSS	Rectal Mucosa Donor 31	rectum
27	chr4:147442200-147444400	Active TSS	A549	lung
28	chr4:147442400-147444400	Active TSS	H9 Cell Line	embryonic stem cell
29	chr4:147442600-147444400	Active TSS	Brain Substantia Nigra	brain
30	chr4:147442800-147444600	Active TSS	Primary T cells from cord blood	blood
31	chr4:147443600-147444400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
32	chr4:147443600-147444400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr4:147443800-147444400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
34	chr4:147443800-147444400	Flanking Active TSS	NH-A	brain
35	chr4:147443800-147444600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
36	chr4:147443800-147444600	Flanking Active TSS	Primary hematopoietic stem cells	blood
37	chr4:147443800-147444600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
38	chr4:147443800-147444600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
39	chr4:147444000-147444400	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
40	chr4:147444000-147444400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr4:147444000-147444400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
42	chr4:147444000-147444400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
43	chr4:147444000-147444400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
44	chr4:147444000-147444400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr4:147444000-147444400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
46	chr4:147444000-147444400	Flanking Active TSS	Primary B cells from peripheral blood	blood
47	chr4:147444000-147444400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
48	chr4:147444000-147444400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
49	chr4:147444000-147444400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
50	chr4:147444000-147444400	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood

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