Variant report

Variant	nsv968904
Chromosome Location	chr5:37170434-37231344
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:268)
CpG islands
(count:549)
Chromatin interactive
region (count:25)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:268 , 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	ARID3A	chr5:37186654-37186894	K562	blood:	n/a	n/a
2	ARID3A	chr5:37187395-37187971	K562	blood:	n/a	n/a
3	ATF1	chr5:37212334-37212527	K562	blood:	n/a	n/a
4	ATF3	chr5:37199018-37199279	K562	blood:	n/a	n/a
5	BACH1	chr5:37226577-37226771	K562	blood:	n/a	n/a
6	BATF	chr5:37184885-37185136	GM12878	blood:	n/a	n/a
7	BCL11A	chr5:37184880-37185082	GM12878	blood:	n/a	n/a
8	BCL11A	chr5:37197865-37198057	GM12878	blood:	n/a	n/a
9	BHLHE40	chr5:37215222-37215328	GM12878	blood:	n/a	n/a
10	BHLHE40	chr5:37182444-37182640	GM12878	blood:	n/a	n/a
11	BHLHE40	chr5:37209321-37209328	K562	blood:	n/a	n/a
12	BHLHE40	chr5:37184866-37185356	GM12878	blood:	n/a	n/a
13	BRCA1	chr5:37174252-37174265	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr5:37225749-37226064	K562	blood:	n/a	n/a
15	CEBPB	chr5:37180286-37180459	H1-hESC	embryonic stem cell:	n/a	chr5:37180403-37180414
16	CEBPB	chr5:37225762-37225958	A549	lung:	n/a	n/a
17	CEBPB	chr5:37199013-37199244	Hela-S3	cervix:	n/a	chr5:37199149-37199160
18	CEBPB	chr5:37180264-37180598	K562	blood:	n/a	chr5:37180403-37180414
19	CEBPB	chr5:37225765-37225992	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr5:37206880-37207191	A549	lung:	n/a	chr5:37207041-37207052 chr5:37207040-37207053
21	CEBPB	chr5:37225857-37226032	K562	blood:	n/a	n/a
22	CEBPB	chr5:37206881-37207206	IMR90	lung:	n/a	chr5:37207041-37207052 chr5:37207040-37207053
23	CEBPB	chr5:37198988-37199323	IMR90	lung:	n/a	chr5:37199149-37199160
24	CEBPB	chr5:37225778-37226022	K562	blood:	n/a	n/a
25	CEBPB	chr5:37206894-37207221	HepG2	liver:	n/a	chr5:37207041-37207052 chr5:37207040-37207053
26	CEBPB	chr5:37206853-37207237	Hela-S3	cervix:	n/a	chr5:37207041-37207052 chr5:37207040-37207053
27	CEBPB	chr5:37198995-37199196	HepG2	liver:	n/a	chr5:37199149-37199160
28	CEBPB	chr5:37197783-37198047	IMR90	lung:	n/a	n/a
29	CEBPB	chr5:37225759-37225962	IMR90	lung:	n/a	n/a
30	CEBPB	chr5:37206917-37207168	K562	blood:	n/a	chr5:37207041-37207052 chr5:37207040-37207053
31	CEBPB	chr5:37225787-37226067	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr5:37180266-37180438	HepG2	liver:	n/a	chr5:37180403-37180414
33	CEBPB	chr5:37198990-37199321	K562	blood:	n/a	chr5:37199149-37199160
34	CEBPB	chr5:37198996-37199280	H1-hESC	embryonic stem cell:	n/a	chr5:37199149-37199160
35	CHD1	chr5:37182440-37182541	GM12878	blood:	n/a	n/a
36	CHD2	chr5:37184807-37185183	GM12878	blood:	n/a	n/a
37	CTCF	chr5:37217842-37217865	LNCaP	prostate:	n/a	n/a
38	CTCF	chr5:37175094-37175349	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr5:37212340-37212490	HVMF	connective:	n/a	n/a
40	CTCF	chr5:37182499-37182582	GM12878	blood:	n/a	n/a
41	CTCF	chr5:37212381-37212451	GM19239	blood:	n/a	n/a
42	CTCF	chr5:37212320-37212470	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr5:37212300-37212450	A549	lung:	n/a	n/a
44	CTCF	chr5:37212360-37212510	BE2_C	brain:	n/a	n/a
45	CTCF	chr5:37212183-37212535	K562	blood:	n/a	n/a
46	CTCF	chr5:37186124-37186297	K562	blood:	n/a	n/a
47	CTCF	chr5:37212277-37212528	K562	blood:	n/a	n/a
48	CTCF	chr5:37212340-37212490	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr5:37212373-37212440	GM19240	blood:	n/a	n/a
50	CTCF	chr5:37212383-37212447	GM10266	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:37206515-37206565	SKMC	muscle:	n/a
2	chr5:37208976-37209026	AG10803	skin:	n/a
3	chr5:37209440-37209490	HL-60	blood:	n/a
4	chr5:37209332-37209382	GM12892	blood:	n/a
5	chr5:37209268-37209318	HUVEC	blood vessel:	n/a
6	chr5:37209440-37209490	GM12878	blood:	n/a
7	chr5:37209332-37209382	HL-60	blood:	n/a
8	chr5:37207622-37207672	HEEpiC	esophagus:	n/a
9	chr5:37209268-37209318	HNPCEpiC	eye:	n/a
10	chr5:37209440-37209490	NHBE	bronchial:	n/a
11	chr5:37209268-37209318	MCF10A-Er-Src	breast:	n/a
12	chr5:37209332-37209382	HEK293	kidney:	embryo
13	chr5:37209332-37209382	HNPCEpiC	eye:	n/a
14	chr5:37209268-37209318	GM12892	blood:	n/a
15	chr5:37208976-37209026	NH-A	brain:	n/a
16	chr5:37206515-37206565	U87	brain:	n/a
17	chr5:37206515-37206565	HIPEpiC	eye:	n/a
18	chr5:37207622-37207672	K562	blood:	n/a
19	chr5:37209440-37209490	ECC-1	luminal epithelium:	n/a
20	chr5:37209182-37209232	HCM	heart:	n/a
21	chr5:37209182-37209232	GM12891	blood:	n/a
22	chr5:37209332-37209382	ProgFib	skin:	n/a
23	chr5:37209332-37209382	AG04450	lung:	fetal
24	chr5:37212448-37212498	PFSK-1	brain:	n/a
25	chr5:37211096-37211146	SK-N-SH_RA	brain:	n/a
26	chr5:37209440-37209490	HAEpiC	amniotic membrane:	n/a
27	chr5:37207622-37207672	SKMC	muscle:	n/a
28	chr5:37209332-37209382	CMK	blood:	n/a
29	chr5:37206515-37206565	SK-N-MC	brain:	n/a
30	chr5:37208976-37209026	CMK	blood:	n/a
31	chr5:37209332-37209382	MCF-7	breast:	n/a
32	chr5:37209182-37209232	SK-N-SH_RA	brain:	n/a
33	chr5:37209182-37209232	HRE	kidney:	n/a
34	chr5:37212448-37212498	RPTEC	kidney:	n/a
35	chr5:37207622-37207672	HPAEpiC	pulmonary alveolar:	n/a
36	chr5:37209332-37209382	U87	brain:	n/a
37	chr5:37212448-37212498	NHDF-neo	bronchial:	n/a
38	chr5:37207622-37207672	MCF10A-Er-Src	breast:	n/a
39	chr5:37207622-37207672	A549	lung:	n/a
40	chr5:37208976-37209026	Hela-S3	cervix:	n/a
41	chr5:37212448-37212498	H1-hESC	embryonic stem cell:	embryo
42	chr5:37208976-37209026	HIPEpiC	eye:	n/a
43	chr5:37209268-37209318	HL-60	blood:	n/a
44	chr5:37209182-37209232	SK-N-MC	brain:	n/a
45	chr5:37209182-37209232	Jurkat	blood:	n/a
46	chr5:37209332-37209382	HRCEpiC	kidney:	n/a
47	chr5:37211096-37211146	MCF10A-Er-Src	breast:	n/a
48	chr5:37209268-37209318	GM12891	blood:	n/a
49	chr5:37206515-37206565	AG09319	gingival:	n/a
50	chr5:37208976-37209026	NHDF-neo	bronchial:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:37178213..37179782-chr5:37187972..37190398,2	K562	blood:
2	chr5:37207387..37209456-chr5:37214290..37217220,2	K562	blood:
3	chr5:37208938..37209800-chrX:13752746..13753402,2	Hela-S3	cervix:
4	chr5:37178213..37179782-chr5:37187972..37190398,2	K562	blood:
5	chr5:37219467..37221366-chr5:37223359..37224948,2	K562	blood:
6	chr5:37225065..37226567-chr5:37275200..37277689,2	K562	blood:
7	chr5:37197697..37200304-chr5:37369735..37371837,2	MCF-7	breast:
8	chr5:37197567..37199786-chr5:37206533..37208192,2	MCF-7	breast:
9	chr5:37197567..37199786-chr5:37206533..37208192,2	MCF-7	breast:
10	chr5:37219759..37221366-chr5:37222603..37224859,2	K562	blood:
11	chr5:37196006..37197813-chr5:37198667..37201494,2	K562	blood:
12	chr5:37217019..37219861-chr5:37224561..37226290,2	MCF-7	breast:
13	chr5:37231083..37232617-chr5:37243518..37245919,2	K562	blood:
14	chr5:37196006..37197813-chr5:37198667..37201494,2	K562	blood:
15	chr5:37189588..37191318-chr5:37194423..37196397,2	K562	blood:
16	chr5:37161788..37164617-chr5:37168284..37171187,2	K562	blood:
17	chr5:37230434..37232617-chr5:37243518..37246467,2	K562	blood:
18	chr5:37229744..37231254-chr5:37247811..37249701,2	MCF-7	breast:
19	chr5:37189588..37191318-chr5:37194423..37196397,2	K562	blood:
20	chr5:37219467..37221366-chr5:37223359..37224948,2	K562	blood:
21	chr5:37217019..37219861-chr5:37224561..37226290,2	MCF-7	breast:
22	chr5:37219759..37221366-chr5:37222603..37224859,2	K562	blood:
23	chr5:37175215..37177693-chr5:37180001..37182944,2	K562	blood:
24	chr5:37198464..37201243-chr5:37207521..37209489,3	MCF-7	breast:
25	chr5:37207387..37209456-chr5:37214290..37217220,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUP155-3	chr5:37173857-37174049	NONHSAT101055
2	lnc-NUP155-3	chr5:37176011-37176201	NONHSAT101055

No data

Variant related genes	Relation type
OFD1P17	TF binding region
C5orf42	TF binding region
OFD1P17	CpG island
C5orf42	CpG island
ENSG00000113569	chromatin interactions
ENSG00000197603	chromatin interactions
ENSG00000046651	chromatin interactions
ENSG00000228212	chromatin interactions
ENSG00000196459	chromatin interactions

Extended variants
information (count: 2128 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:2128 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544249065	chr5:37170440-37170441	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs372426953	chr5:37170457-37170458	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs189321984	chr5:37170463-37170464	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs541619301	chr5:37170508-37170509	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs560044439	chr5:37170540-37170541	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs370183812	chr5:37170564-37170565	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs139622828	chr5:37170575-37170576	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs116648820	chr5:37170578-37170579	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs569232515	chr5:37170586-37170587	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs540889712	chr5:37170604-37170605	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs180813216	chr5:37170642-37170643	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs367881094	chr5:37170715-37170716	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs185435722	chr5:37170762-37170763	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs191030714	chr5:37170792-37170793	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs371990663	chr5:37170809-37170810	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs550209733	chr5:37170823-37170824	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs568455139	chr5:37170881-37170882	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs143343523	chr5:37170913-37170914	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs554325696	chr5:37170914-37170915	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs146729889	chr5:37170915-37170916	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs566389376	chr5:37170919-37170920	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs183546702	chr5:37170970-37170971	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs549426648	chr5:37170980-37170981	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs562955216	chr5:37171041-37171042	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs373832853	chr5:37171043-37171044	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs558587610	chr5:37171052-37171053	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs185900390	chr5:37171064-37171065	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs537432596	chr5:37171119-37171120	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs531752628	chr5:37171137-37171138	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs572577114	chr5:37171143-37171144	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs374185105	chr5:37171187-37171188	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs551548507	chr5:37171192-37171193	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs571306102	chr5:37171193-37171194	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs556269845	chr5:37171228-37171229	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs574429222	chr5:37171268-37171269	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs541657944	chr5:37171269-37171270	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs559882144	chr5:37171293-37171294	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs368321276	chr5:37171329-37171330	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs10056009	chr5:37171342-37171343	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs13166974	chr5:37171365-37171366	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs564335120	chr5:37171397-37171398	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs531773267	chr5:37171425-37171426	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191667150	chr5:37171457-37171458	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs183123218	chr5:37171458-37171459	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562242526	chr5:37171503-37171504	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529332629	chr5:37171554-37171555	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369278024	chr5:37171555-37171556	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111470267	chr5:37171652-37171653	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535832818	chr5:37171780-37171781	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs141707325	chr5:37171848-37171849	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	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
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Lung cancer	19153074	CNVD
Cornelia de Lange syndrome	21085971	CNVD
Autism	21701786	CNVD
Cervical cancer	16585170	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1659 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:37112200-37198200	Weak transcription	Small Intestine	intestine
2	chr5:37113600-37222200	Weak transcription	Psoas Muscle	Psoas
3	chr5:37134200-37171200	Weak transcription	Colonic Mucosa	Colon
4	chr5:37136200-37197200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr5:37137400-37174000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr5:37138400-37196800	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr5:37138600-37179600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr5:37143400-37189600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr5:37144400-37171400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr5:37146400-37174000	Weak transcription	GM12878-XiMat	blood
11	chr5:37147200-37200600	Strong transcription	HSMM	muscle
12	chr5:37148000-37182000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr5:37148600-37189400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr5:37150600-37176400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr5:37151600-37197400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr5:37153000-37170600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr5:37157400-37171400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr5:37158000-37177600	Weak transcription	Fetal Brain Male	brain
19	chr5:37159600-37197400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr5:37161000-37207200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr5:37161200-37174200	Strong transcription	Muscle Satellite Cultured Cells	--
22	chr5:37161200-37179400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr5:37161200-37183800	Strong transcription	Dnd41	blood
24	chr5:37161200-37197400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr5:37161400-37178200	Strong transcription	NHDF-Ad	bronchial
26	chr5:37161600-37171600	Strong transcription	Hela-S3	cervix
27	chr5:37161600-37177600	Strong transcription	Fetal Brain Female	brain
28	chr5:37161600-37179600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr5:37162000-37179800	Strong transcription	Placenta	Placenta
30	chr5:37162200-37179800	Strong transcription	Fetal Muscle Leg	muscle
31	chr5:37162400-37188600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr5:37162600-37178600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr5:37162600-37180200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
34	chr5:37162600-37197400	Strong transcription	Adipose Nuclei	Adipose
35	chr5:37163000-37179800	Strong transcription	Fetal Thymus	thymus
36	chr5:37163200-37178000	Strong transcription	Duodenum Smooth Muscle	Duodenum
37	chr5:37163200-37179600	Strong transcription	Skeletal Muscle Female	skeletal muscle
38	chr5:37163400-37177000	Strong transcription	Primary hematopoietic stem cells	blood
39	chr5:37165200-37171800	Strong transcription	Brain Angular Gyrus	brain
40	chr5:37165200-37179600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr5:37165400-37179600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr5:37166400-37176600	Strong transcription	NH-A	brain
43	chr5:37166400-37198400	Weak transcription	Stomach Mucosa	stomach
44	chr5:37166400-37213600	Weak transcription	HepG2	liver
45	chr5:37166600-37197400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr5:37167000-37171200	Weak transcription	HMEC	breast
47	chr5:37167000-37171800	Strong transcription	HUES64 Cell Line	embryonic stem cell
48	chr5:37167000-37194800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr5:37167200-37175600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr5:37167200-37179400	Strong transcription	Fetal Muscle Trunk	muscle

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