Variant report

Variant	nsv883194
Chromosome Location	chr5:177604268-177620189
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:244)
CpG islands
(count:672)
Chromatin interactive
region (count:19)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:177613656-177613764	K562	blood:	n/a	n/a
2	ARID3A	chr5:177609086-177609495	K562	blood:	n/a	n/a
3	ATF1	chr5:177609086-177609636	K562	blood:	n/a	n/a
4	ATF2	chr5:177607179-177607878	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr5:177607185-177607944	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr5:177612633-177612748	K562	blood:	n/a	n/a
7	BHLHE40	chr5:177605007-177605026	K562	blood:	n/a	n/a
8	BHLHE40	chr5:177609261-177609512	K562	blood:	n/a	n/a
9	CBX3	chr5:177619833-177620136	K562	blood:	n/a	n/a
10	CBX3	chr5:177609035-177609734	K562	blood:	n/a	n/a
11	CCNT2	chr5:177609020-177609562	K562	blood:	n/a	n/a
12	CEBPB	chr5:177619215-177619709	MCF-7	breast:	n/a	chr5:177619447-177619458
13	CEBPB	chr5:177607306-177608020	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr5:177619237-177619584	MCF-7	breast:	n/a	chr5:177619447-177619458
15	CEBPB	chr5:177609085-177609284	K562	blood:	n/a	n/a
16	CEBPB	chr5:177619259-177619643	Hela-S3	cervix:	n/a	chr5:177619447-177619458
17	CEBPB	chr5:177619282-177619592	HepG2	liver:	n/a	chr5:177619447-177619458
18	CEBPB	chr5:177609042-177609666	K562	blood:	n/a	n/a
19	CEBPB	chr5:177609042-177609649	K562	blood:	n/a	n/a
20	CEBPB	chr5:177609456-177609977	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr5:177619284-177619523	A549	lung:	n/a	chr5:177619447-177619458
22	CEBPB	chr5:177619253-177619553	ECC-1	luminal epithelium:	n/a	chr5:177619447-177619458
23	CEBPB	chr5:177619156-177619824	HCT-116	colon:	n/a	chr5:177619447-177619458
24	CEBPB	chr5:177609377-177609553	K562	blood:	n/a	n/a
25	CEBPB	chr5:177619228-177619641	ECC-1	luminal epithelium:	n/a	chr5:177619447-177619458
26	CEBPB	chr5:177619293-177619625	K562	blood:	n/a	chr5:177619447-177619458
27	CEBPB	chr5:177619205-177619583	K562	blood:	n/a	chr5:177619447-177619458
28	CEBPB	chr5:177604542-177604742	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr5:177607637-177607853	K562	blood:	n/a	n/a
30	CEBPB	chr5:177619168-177619724	HCT-116	colon:	n/a	chr5:177619447-177619458
31	CEBPB	chr5:177619265-177619611	IMR90	lung:	n/a	chr5:177619447-177619458
32	CEBPD	chr5:177609083-177609689	K562	blood:	n/a	n/a
33	CEBPD	chr5:177608961-177609729	K562	blood:	n/a	n/a
34	CHD1	chr5:177607284-177607689	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr5:177609294-177609297	K562	blood:	n/a	n/a
36	CHD2	chr5:177606635-177607782	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr5:177607176-177607981	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr5:177607501-177607933	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTBP2	chr5:177607254-177607814	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr5:177604640-177604790	HEK293	kidney:	n/a	n/a
41	CTCF	chr5:177604544-177604902	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr5:177604659-177604739	MCF-7	breast:	n/a	n/a
43	CTCF	chr5:177604666-177604771	MCF-7	breast:	n/a	n/a
44	CTCF	chr5:177604660-177604810	HepG2	liver:	n/a	n/a
45	CTCF	chr5:177604648-177604760	MCF-7	breast:	n/a	n/a
46	CTCF	chr5:177604653-177604755	MCF-7	breast:	n/a	n/a
47	CTCF	chr5:177604584-177604796	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr5:177608936-177609022	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr5:177604684-177604753	NHEK	skin:	n/a	n/a
50	CTCF	chr5:177604647-177604763	Hela-S3	cervix:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:177615518-177615568	T-47D	breast:	n/a
2	chr5:177615518-177615568	T-47D	breast:	n/a
3	chr5:177610810-177610860	NB4	blood:	n/a
4	chr5:177613003-177613053	AG10803	skin:	n/a
5	chr5:177614292-177614342	CMK	blood:	n/a
6	chr5:177615518-177615568	BE2_C	brain:	n/a
7	chr5:177614217-177614267	HCPEpiC	choroid plexus:	n/a
8	chr5:177615731-177615781	AG10803	skin:	n/a
9	chr5:177615518-177615568	MCF10A-Er-Src	breast:	n/a
10	chr5:177615005-177615055	BJ	skin:	n/a
11	chr5:177614217-177614267	HRE	kidney:	n/a
12	chr5:177614217-177614267	Caco-2	colon:	n/a
13	chr5:177615731-177615781	NH-A	brain:	n/a
14	chr5:177617272-177617322	HMEC	breast:	n/a
15	chr5:177613003-177613053	HCM	heart:	n/a
16	chr5:177615518-177615568	HUVEC	blood vessel:	n/a
17	chr5:177617272-177617322	U87	brain:	n/a
18	chr5:177613003-177613053	HCT-116	colon:	n/a
19	chr5:177617272-177617322	Hela-S3	cervix:	n/a
20	chr5:177615731-177615781	GM12878	blood:	n/a
21	chr5:177615005-177615055	LNCaP	prostate:	n/a
22	chr5:177612982-177613032	AG10803	skin:	n/a
23	chr5:177614382-177614432	HUVEC	blood vessel:	n/a
24	chr5:177614382-177614432	PANC-1	pancreas:	n/a
25	chr5:177614217-177614267	NT2-D1	testis:	n/a
26	chr5:177614217-177614267	PFSK-1	brain:	n/a
27	chr5:177617272-177617322	HAEpiC	amniotic membrane:	n/a
28	chr5:177610810-177610860	Hela-S3	cervix:	n/a
29	chr5:177610810-177610860	ovcar-3	ovarian:	n/a
30	chr5:177610810-177610860	HL-60	blood:	n/a
31	chr5:177614217-177614267	MCF10A-Er-Src	breast:	n/a
32	chr5:177614292-177614342	MCF-7	breast:	n/a
33	chr5:177617272-177617322	HEEpiC	esophagus:	n/a
34	chr5:177617272-177617322	GM12878	blood:	n/a
35	chr5:177614382-177614432	MCF10A-Er-Src	breast:	n/a
36	chr5:177613003-177613053	HNPCEpiC	eye:	n/a
37	chr5:177614205-177614255	HEK293	kidney:	embryo
38	chr5:177614205-177614255	U87	brain:	n/a
39	chr5:177613003-177613053	ECC-1	luminal epithelium:	n/a
40	chr5:177613003-177613053	PFSK-1	brain:	n/a
41	chr5:177614205-177614255	HPAEpiC	pulmonary alveolar:	n/a
42	chr5:177612982-177613032	SAEC	small airway:	n/a
43	chr5:177614382-177614432	HEK293	kidney:	embryo
44	chr5:177613003-177613053	NHBE	bronchial:	n/a
45	chr5:177615518-177615568	HEEpiC	esophagus:	n/a
46	chr5:177617272-177617322	ProgFib	skin:	n/a
47	chr5:177614292-177614342	ovcar-3	ovarian:	n/a
48	chr5:177610810-177610860	NHBE	bronchial:	n/a
49	chr5:177617272-177617322	PANC-1	pancreas:	n/a
50	chr5:177610810-177610860	AG10803	skin:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:177613072..177615957-chr5:177659065..177661764,2	MCF-7	breast:
2	chr5:177602250..177605142-chr5:177611830..177614251,2	K562	blood:
3	chr5:177611266..177612988-chr5:177631125..177633066,2	K562	blood:
4	chr5:177602250..177605142-chr5:177611830..177614251,2	K562	blood:
5	chr5:177607704..177609339-chr5:177631381..177632987,2	MCF-7	breast:
6	chr5:177604347..177606452-chr5:177626803..177628978,2	MCF-7	breast:
7	chr5:177610597..177612167-chr5:177612289..177614022,2	MCF-7	breast:
8	chr5:177603738..177606213-chr5:177630891..177632617,3	MCF-7	breast:
9	chr5:177617264..177619059-chr5:177621783..177623685,3	K562	blood:
10	chr5:177604192..177606975-chr5:177607801..177609756,2	MCF-7	breast:
11	chr5:177605204..177607024-chr5:177611058..177613922,2	MCF-7	breast:
12	chr5:177610597..177612167-chr5:177612289..177614022,2	MCF-7	breast:
13	chr5:177614467..177617633-chr5:177630429..177633040,4	K562	blood:
14	chr19:18433441..18434193-chr5:177619863..177620363,2	HCT-116	colon:
15	chr5:177605439..177607840-chr5:177629725..177632123,2	K562	blood:
16	chr5:177612069..177614824-chr5:177616519..177619259,2	MCF-7	breast:
17	chr5:177604192..177606975-chr5:177607801..177609756,2	MCF-7	breast:
18	chr5:177606946..177609257-chr5:177631004..177633019,2	MCF-7	breast:
19	chr5:177605204..177607024-chr5:177611058..177613922,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AGXT2L2-1	chr5:177611511-177614433	NONHSAT105522

No data

Variant related genes	Relation type
GMCL1P1	TF binding region
GMCL1P1	CpG island
ENSG00000197451	chromatin interactions
ENSG00000130520	chromatin interactions
ENSG00000244234	chromatin interactions
ENSG00000175309	chromatin interactions

Extended variants
information (count: 643 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:643 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17080239	chr5:177604268-177604269	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs188288417	chr5:177604294-177604295	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs537480425	chr5:177604323-177604324	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs555982811	chr5:177604332-177604333	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs532614792	chr5:177604376-177604377	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs567889167	chr5:177604377-177604378	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs191237339	chr5:177604398-177604399	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs553277224	chr5:177604399-177604400	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs71585681	chr5:177604406-177604407	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs142873044	chr5:177604408-177604409	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
11	rs151025987	chr5:177604513-177604514	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs556680184	chr5:177604514-177604515	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs11948118	chr5:177604555-177604556	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs574853958	chr5:177604660-177604661	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs183775767	chr5:177604661-177604662	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs10074810	chr5:177604679-177604680	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs116625641	chr5:177604686-177604687	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs528391320	chr5:177604723-177604724	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs372862004	chr5:177604746-177604747	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs75617701	chr5:177604762-177604763	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs189271563	chr5:177604764-177604765	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs551894584	chr5:177604785-177604786	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs377226141	chr5:177604818-177604819	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs72648829	chr5:177604827-177604828	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs181779534	chr5:177604865-177604866	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs554580979	chr5:177604909-177604910	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs185786880	chr5:177604916-177604917	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs35085759	chr5:177604919-177604920	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs189814732	chr5:177604927-177604928	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs78779824	chr5:177604990-177604991	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs76785446	chr5:177605016-177605017	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs36131810	chr5:177605073-177605074	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs199855757	chr5:177605076-177605077	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs549328331	chr5:177605077-177605078	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs556593287	chr5:177605086-177605087	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs150270289	chr5:177605106-177605107	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs536210609	chr5:177605117-177605118	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs554250997	chr5:177605118-177605119	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs79874425	chr5:177605148-177605149	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs74836585	chr5:177605252-177605253	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs71585682	chr5:177605258-177605259	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs70994983	chr5:177605264-177605265	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs116433821	chr5:177605309-177605310	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs544420879	chr5:177605367-177605368	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs182012838	chr5:177605383-177605384	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs530896742	chr5:177605454-177605455	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs540063693	chr5:177605491-177605492	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs186317071	chr5:177605528-177605529	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs73804729	chr5:177605537-177605538	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs528528635	chr5:177605544-177605545	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
Thoracic aortic aneurysm	21092924	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:174 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:177593000-177604800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:177598000-177604600	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr5:177598200-177606600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr5:177601000-177606600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr5:177603600-177605400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr5:177603600-177605600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr5:177604000-177604600	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr5:177604000-177605400	Enhancers	Primary hematopoietic stem cells	blood
9	chr5:177604000-177605400	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr5:177604000-177605600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr5:177604600-177605000	Enhancers	Thymus	Thymus
12	chr5:177604600-177605400	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr5:177604800-177605200	Enhancers	Fetal Thymus	thymus
14	chr5:177604800-177605400	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr5:177604800-177605400	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr5:177604800-177605400	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr5:177604800-177605400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr5:177604800-177605400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr5:177604800-177605600	Enhancers	H1 Cell Line	embryonic stem cell
20	chr5:177604800-177605600	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr5:177604800-177605600	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr5:177605200-177605600	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr5:177605200-177609000	Weak transcription	Fetal Thymus	thymus
24	chr5:177605400-177606400	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr5:177605400-177606400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr5:177605400-177606600	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr5:177605400-177606800	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr5:177605400-177606800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr5:177605400-177607400	Weak transcription	Primary hematopoietic stem cells	blood
30	chr5:177605400-177608400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr5:177605400-177608800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr5:177605400-177609400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr5:177605600-177606600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr5:177605600-177606600	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr5:177605600-177606600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr5:177605600-177606600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr5:177605600-177606600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr5:177605600-177606600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr5:177606400-177606600	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr5:177606400-177607200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
41	chr5:177606600-177606800	Enhancers	H1 Cell Line	embryonic stem cell
42	chr5:177606600-177606800	Enhancers	H9 Cell Line	embryonic stem cell
43	chr5:177606600-177606800	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr5:177606600-177606800	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr5:177606600-177607000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
46	chr5:177606600-177607000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
47	chr5:177606600-177607000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
48	chr5:177606600-177607200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr5:177606600-177607600	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr5:177606600-177607800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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