Variant report

Variant	nsv969028
Chromosome Location	chr5:179117224-179123617
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:18)
CpG islands
(count:123)
Chromatin interactive
region (count:20)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr5:179121369-179121482	HepG2	liver:	n/a	n/a
2	CTCF	chr5:179121431-179121505	HepG2	liver:	n/a	n/a
3	FOXA1	chr5:179123600-179124022	HepG2	liver:	n/a	chr5:179123779-179123794
4	FOXA1	chr5:179123604-179123896	HepG2	liver:	n/a	chr5:179123779-179123794
5	NR2F2	chr5:179122828-179123146	K562	blood:	n/a	n/a
6	POLR2A	chr5:179123580-179123923	GM12892	blood:	n/a	n/a
7	POLR2A	chr5:179122915-179122985	HepG2	liver:	n/a	n/a
8	POLR2A	chr5:179123377-179123961	HepG2	liver:	n/a	n/a
9	POLR2A	chr5:179122991-179123128	HepG2	liver:	n/a	n/a
10	POLR2A	chr5:179123448-179124704	PANC-1	pancreas:	n/a	n/a
11	POLR2A	chr5:179122449-179122537	K562	blood:	n/a	n/a
12	POLR2A	chr5:179121922-179122017	K562	blood:	n/a	n/a
13	RAD21	chr5:179121309-179121528	HepG2	liver:	n/a	n/a
14	REST	chr5:179120976-179121091	U87	brain:	n/a	n/a
15	SPI1	chr5:179123530-179124161	HL-60	blood:	n/a	n/a
16	SPI1	chr5:179123576-179124088	HL-60	blood:	n/a	n/a
17	ZNF263	chr5:179121620-179122001	HEK293-T-REx	kidney:	n/a	n/a
18	ZNF384	chr5:179118533-179118647	K562	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:179121005-179121055	T-47D	breast:	n/a
2	chr5:179121005-179121055	T-47D	breast:	n/a
3	chr5:179121005-179121055	H1-hESC	embryonic stem cell:	embryo
4	chr5:179121385-179121435	HEEpiC	esophagus:	n/a
5	chr5:179121005-179121055	HCT-116	colon:	n/a
6	chr5:179121385-179121435	IMR90	lung:	fetal
7	chr5:179121005-179121055	GM12891	blood:	n/a
8	chr5:179121005-179121055	HepG2	liver:	n/a
9	chr5:179121005-179121055	HNPCEpiC	eye:	n/a
10	chr5:179121005-179121055	LNCaP	prostate:	n/a
11	chr5:179121005-179121055	HCM	heart:	n/a
12	chr5:179121005-179121055	RPTEC	kidney:	n/a
13	chr5:179121005-179121055	NT2-D1	testis:	n/a
14	chr5:179121385-179121435	SK-N-SH_RA	brain:	n/a
15	chr5:179121005-179121055	AG09309	skin:	n/a
16	chr5:179121385-179121435	SKMC	muscle:	n/a
17	chr5:179121005-179121055	SK-N-SH_RA	brain:	n/a
18	chr5:179121385-179121435	LNCaP	prostate:	n/a
19	chr5:179121385-179121435	PFSK-1	brain:	n/a
20	chr5:179121385-179121435	GM12892	blood:	n/a
21	chr5:179121005-179121055	HIPEpiC	eye:	n/a
22	chr5:179121005-179121055	PANC-1	pancreas:	n/a
23	chr5:179121385-179121435	HEK293	kidney:	embryo
24	chr5:179121005-179121055	CMK	blood:	n/a
25	chr5:179121005-179121055	SKMC	muscle:	n/a
26	chr5:179121005-179121055	AG09319	gingival:	n/a
27	chr5:179121385-179121435	GM12878	blood:	n/a
28	chr5:179121005-179121055	A549	lung:	n/a
29	chr5:179121385-179121435	Hela-S3	cervix:	n/a
30	chr5:179121385-179121435	AG09309	skin:	n/a
31	chr5:179121005-179121055	ProgFib	skin:	n/a
32	chr5:179121385-179121435	Hepatocyte	liver:	n/a
33	chr5:179121385-179121435	CMK	blood:	n/a
34	chr5:179121005-179121055	SK-N-MC	brain:	n/a
35	chr5:179121385-179121435	HRE	kidney:	n/a
36	chr5:179121005-179121055	SAEC	small airway:	n/a
37	chr5:179121385-179121435	PANC-1	pancreas:	n/a
38	chr5:179121005-179121055	HL-60	blood:	n/a
39	chr5:179121385-179121435	NT2-D1	testis:	n/a
40	chr5:179121385-179121435	HepG2	liver:	n/a
41	chr5:179121005-179121055	HEK293	kidney:	embryo
42	chr5:179121385-179121435	HCM	heart:	n/a
43	chr5:179121005-179121055	BJ	skin:	n/a
44	chr5:179121385-179121435	HAEpiC	amniotic membrane:	n/a
45	chr5:179121005-179121055	Caco-2	colon:	n/a
46	chr5:179121385-179121435	U87	brain:	n/a
47	chr5:179121005-179121055	MCF-7	breast:	n/a
48	chr5:179121385-179121435	HRPEpiC	eye:	n/a
49	chr5:179121005-179121055	PFSK-1	brain:	n/a
50	chr5:179121005-179121055	HPAEpiC	pulmonary alveolar:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:179100989..179111182-chr5:179122076..179128627,19	K562	blood:
2	chr5:179049048..179052854-chr5:179122221..179127718,16	MCF-7	breast:
3	chr5:179094562..179097080-chr5:179122833..179124461,2	MCF-7	breast:
4	chr5:179114860..179117850-chr5:179121484..179123259,2	K562	blood:
5	chr5:179123586..179129079-chr5:179129217..179136579,19	MCF-7	breast:
6	chr5:179122873..179128898-chr5:179155888..179164921,20	K562	blood:
7	chr5:179050688..179053100-chr5:179121935..179123833,2	K562	blood:
8	chr5:179123572..179126776-chr5:179221240..179224069,3	MCF-7	breast:
9	chr5:179106241..179110085-chr5:179114394..179117235,5	MCF-7	breast:
10	chr5:179101962..179108661-chr5:179122383..179128408,19	MCF-7	breast:
11	chr5:179122850..179128148-chr5:179246584..179249342,5	K562	blood:
12	chr5:179121868..179123530-chr5:179124381..179126535,2	K562	blood:
13	chr5:179104994..179107833-chr5:179116726..179118751,2	K562	blood:
14	chr5:179116479..179118701-chr5:179124971..179127745,3	K562	blood:
15	chr5:179121400..179128828-chr5:179157984..179161377,21	K562	blood:
16	chr5:178955819..178957353-chr5:179123603..179125281,2	MCF-7	breast:
17	chr5:179114860..179117850-chr5:179121484..179123259,2	K562	blood:
18	chr5:179101603..179111989-chr5:179122927..179129527,32	MCF-7	breast:
19	chr5:179108514..179110108-chr5:179117962..179119813,2	K562	blood:
20	chr5:179114401..179118460-chr5:179124175..179127183,5	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC136604.1-2	chr5:179121307-179121650	NONHSAT105615
2	lnc-CBY3-2	chr5:179123601-179124700	NONHSAT105616

No data

Variant related genes	Relation type
CANX	TF binding region
HMGB3P22	TF binding region
CANX	CpG island
HMGB3P22	CpG island
ENSG00000213316	chromatin interactions
ENSG00000204659	chromatin interactions
ENSG00000169045	chromatin interactions
ENSG00000161021	chromatin interactions
ENSG00000127022	chromatin interactions
ENSG00000225051	chromatin interactions
ENSG00000161011	chromatin interactions

Extended variants
information (count: 257 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:257 , 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	rs535857926	chr5:179117265-179117266	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs11959335	chr5:179117305-179117306	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs368041713	chr5:179117315-179117316	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs537337291	chr5:179117393-179117394	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs562396092	chr5:179117428-179117429	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs549291948	chr5:179117436-179117437	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs112211556	chr5:179117447-179117448	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs191489783	chr5:179117448-179117449	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs556133603	chr5:179117469-179117470	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs577999276	chr5:179117471-179117472	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs539169727	chr5:179117531-179117532	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs541389938	chr5:179117552-179117553	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs575233289	chr5:179117599-179117600	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs58874777	chr5:179117600-179117601	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs141802448	chr5:179117613-179117614	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs183923768	chr5:179117631-179117632	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs376593945	chr5:179117635-179117636	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs145476379	chr5:179117644-179117645	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs561140068	chr5:179117719-179117720	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs569602996	chr5:179117747-179117748	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs188205783	chr5:179117753-179117754	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs72662130	chr5:179117759-179117760	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs72662131	chr5:179117763-179117764	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs375928217	chr5:179117839-179117840	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs550692612	chr5:179117886-179117887	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs562322519	chr5:179117971-179117972	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs529661816	chr5:179118009-179118010	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs192682757	chr5:179118100-179118101	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs369813162	chr5:179118108-179118109	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs113341439	chr5:179118152-179118153	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs112964079	chr5:179118175-179118176	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs113331702	chr5:179118189-179118190	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs546786451	chr5:179118228-179118229	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs571849964	chr5:179118245-179118246	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs538740708	chr5:179118259-179118260	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs58499840	chr5:179118269-179118270	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs139765544	chr5:179118306-179118307	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs6872508	chr5:179118316-179118317	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs536615709	chr5:179118429-179118430	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs74952000	chr5:179118483-179118484	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs149352289	chr5:179118512-179118513	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs540733644	chr5:179118532-179118533	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs185646772	chr5:179118535-179118536	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs4235518	chr5:179118554-179118555	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs10050544	chr5:179118588-179118589	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs544095506	chr5:179118655-179118656	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs78700978	chr5:179118661-179118662	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs529747805	chr5:179118708-179118709	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs4296767	chr5:179118715-179118716	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs190021868	chr5:179118727-179118728	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:179106400-179118200	Weak transcription	Right Ventricle	heart
2	chr5:179106600-179124200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr5:179106600-179124800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr5:179106800-179123000	Weak transcription	Fetal Muscle Leg	muscle
5	chr5:179107400-179121400	Weak transcription	Primary B cells from cord blood	blood
6	chr5:179107600-179117600	Weak transcription	Primary hematopoietic stem cells	blood
7	chr5:179107600-179119600	Weak transcription	Brain Cingulate Gyrus	brain
8	chr5:179107600-179123200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr5:179107600-179123200	Weak transcription	Fetal Thymus	thymus
10	chr5:179107600-179123400	Weak transcription	Fetal Intestine Small	intestine
11	chr5:179108400-179123000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr5:179108600-179123600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr5:179113800-179118200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr5:179114000-179123000	Weak transcription	HepG2	liver
15	chr5:179117000-179121200	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr5:179118200-179118400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr5:179118400-179125000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr5:179120200-179120800	Enhancers	Skeletal Muscle Male	skeletal muscle
19	chr5:179120800-179122000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr5:179120800-179123800	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr5:179121200-179121400	Enhancers	Primary neutrophils fromperipheralblood	blood
22	chr5:179121200-179122000	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr5:179121200-179122800	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr5:179121400-179121600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
25	chr5:179121400-179122200	Enhancers	Primary B cells from cord blood	blood
26	chr5:179121400-179123800	Weak transcription	Brain Cingulate Gyrus	brain
27	chr5:179121600-179121800	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr5:179121800-179122000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
29	chr5:179121800-179122000	Enhancers	K562	blood
30	chr5:179122000-179123000	Weak transcription	K562	blood
31	chr5:179122000-179123000	Weak transcription	Monocytes-CD14+_RO01746	blood
32	chr5:179122000-179124200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr5:179122000-179124200	Enhancers	Primary neutrophils fromperipheralblood	blood
34	chr5:179122200-179123400	Weak transcription	Primary B cells from cord blood	blood
35	chr5:179122800-179123200	Weak transcription	Primary monocytes fromperipheralblood	blood
36	chr5:179123000-179123200	Enhancers	Pancreas	Pancrea
37	chr5:179123000-179123200	Enhancers	Psoas Muscle	Psoas
38	chr5:179123000-179123600	Enhancers	Fetal Muscle Leg	muscle
39	chr5:179123000-179123600	Enhancers	GM12878-XiMat	blood
40	chr5:179123000-179124400	Enhancers	K562	blood
41	chr5:179123000-179124400	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr5:179123000-179124600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr5:179123000-179124600	Enhancers	HepG2	liver
44	chr5:179123200-179123800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr5:179123200-179124200	Weak transcription	Pancreas	Pancrea
46	chr5:179123200-179124200	Weak transcription	Psoas Muscle	Psoas
47	chr5:179123200-179124800	Enhancers	Fetal Thymus	thymus
48	chr5:179123200-179125000	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr5:179123200-179125000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr5:179123200-179125000	Enhancers	Fetal Muscle Trunk	muscle

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