Variant report

Variant	nsv1018194
Chromosome Location	chr5:76090951-76129241
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1370)
CpG islands
(count:1468)
Chromatin interactive
region (count:19)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1370 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:76113989-76114292	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:76114553-76114860	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:76116209-76116734	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:76126576-76126776	K562	blood:	n/a	n/a
5	ARID3A	chr5:76101782-76102245	K562	blood:	n/a	n/a
6	ATF1	chr5:76101722-76102174	K562	blood:	n/a	n/a
7	ATF2	chr5:76126950-76127363	GM12878	blood:	n/a	n/a
8	ATF2	chr5:76126912-76127331	GM12878	blood:	n/a	n/a
9	ATF2	chr5:76103843-76104561	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr5:76103823-76104436	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr5:76113947-76114568	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr5:76114079-76115052	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr5:76101689-76102467	A549	lung:	n/a	n/a
14	ATF3	chr5:76100044-76100672	A549	lung:	n/a	n/a
15	ATF3	chr5:76101627-76102562	A549	lung:	n/a	n/a
16	ATF3	chr5:76114432-76115010	A549	lung:	n/a	chr5:76114977-76114986 chr5:76114862-76114870
17	ATF3	chr5:76114447-76115003	A549	lung:	n/a	chr5:76114977-76114986 chr5:76114862-76114870
18	ATF3	chr5:76099975-76100655	A549	lung:	n/a	n/a
19	BACH1	chr5:76126596-76126774	K562	blood:	n/a	n/a
20	BACH1	chr5:76114200-76116153	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr5:76103704-76103712	K562	blood:	n/a	n/a
22	BATF	chr5:76102000-76102358	GM12878	blood:	n/a	n/a
23	BATF	chr5:76126956-76127325	GM12878	blood:	n/a	n/a
24	BCL11A	chr5:76126997-76127227	GM12878	blood:	n/a	chr5:76127105-76127114
25	BCL11A	chr5:76126931-76127279	GM12878	blood:	n/a	chr5:76127105-76127114
26	BCL3	chr5:76126983-76127322	GM12878	blood:	n/a	chr5:76127105-76127114
27	BCL3	chr5:76115978-76116822	A549	lung:	n/a	n/a
28	BCL3	chr5:76109782-76110506	A549	lung:	n/a	chr5:76110348-76110357
29	BCL3	chr5:76099724-76100840	A549	lung:	n/a	chr5:76100092-76100100 chr5:76100201-76100210
30	BCL3	chr5:76126827-76127402	A549	lung:	n/a	chr5:76127105-76127114
31	BCL3	chr5:76099974-76100817	A549	lung:	n/a	chr5:76100092-76100100 chr5:76100201-76100210
32	BCL3	chr5:76101997-76102356	GM12878	blood:	n/a	chr5:76102262-76102271
33	BCL3	chr5:76109914-76110498	A549	lung:	n/a	chr5:76110348-76110357
34	BCL3	chr5:76101399-76102582	A549	lung:	n/a	chr5:76102262-76102271
35	BCL3	chr5:76114082-76115135	A549	lung:	n/a	chr5:76114962-76114971 chr5:76114691-76114704
36	BCL3	chr5:76097061-76097862	A549	lung:	n/a	n/a
37	BCL3	chr5:76126569-76127455	A549	lung:	n/a	chr5:76127105-76127114
38	BCL3	chr5:76101545-76102516	A549	lung:	n/a	chr5:76102262-76102271
39	BCL3	chr5:76126926-76127294	GM12878	blood:	n/a	chr5:76127105-76127114
40	BCL3	chr5:76101972-76102349	GM12878	blood:	n/a	chr5:76102262-76102271
41	BCLAF1	chr5:76126973-76127278	GM12878	blood:	n/a	chr5:76127105-76127114
42	BHLHE40	chr5:76101694-76102239	K562	blood:	n/a	n/a
43	BHLHE40	chr5:76126969-76127195	A549	lung:	n/a	n/a
44	BHLHE40	chr5:76126954-76127367	GM12878	blood:	n/a	n/a
45	BHLHE40	chr5:76121429-76121600	A549	lung:	n/a	n/a
46	BHLHE40	chr5:76090863-76090978	K562	blood:	n/a	n/a
47	BRCA1	chr5:76101731-76102250	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr5:76114112-76114340	H1-hESC	embryonic stem cell:	n/a	n/a
49	BRCA1	chr5:76110002-76110390	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr5:76115005-76115163	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1468 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:76114635-76114685	HRE	kidney:	n/a
2	chr5:76115810-76115860	NHBE	bronchial:	n/a
3	chr5:76111995-76112045	T-47D	breast:	n/a
4	chr5:76116535-76116585	NHDF-neo	bronchial:	n/a
5	chr5:76114635-76114685	HRE	kidney:	n/a
6	chr5:76115810-76115860	NHBE	bronchial:	n/a
7	chr5:76111995-76112045	T-47D	breast:	n/a
8	chr5:76116535-76116585	NHDF-neo	bronchial:	n/a
9	chr5:76112996-76113046	Hepatocyte	liver:	n/a
10	chr5:76112776-76112826	GM12891	blood:	n/a
11	chr5:76114646-76114696	HEEpiC	esophagus:	n/a
12	chr5:76112996-76113046	PrEC	prostate:	n/a
13	chr5:76114522-76114572	HL-60	blood:	n/a
14	chr5:76115974-76116024	SK-N-SH_RA	brain:	n/a
15	chr5:76112996-76113046	HCT-116	colon:	n/a
16	chr5:76115810-76115860	MCF-7	breast:	n/a
17	chr5:76117747-76117797	Caco-2	colon:	n/a
18	chr5:76115810-76115860	AoSMC	blood vessel:	n/a
19	chr5:76119931-76119981	HRPEpiC	eye:	n/a
20	chr5:76115309-76115359	NB4	blood:	n/a
21	chr5:76116535-76116585	Hepatocyte	liver:	n/a
22	chr5:76114522-76114572	HepG2	liver:	n/a
23	chr5:76114373-76114423	PFSK-1	brain:	n/a
24	chr5:76112776-76112826	CMK	blood:	n/a
25	chr5:76114822-76114872	ovcar-3	ovarian:	n/a
26	chr5:76108729-76108779	T-47D	breast:	n/a
27	chr5:76116088-76116138	Hela-S3	cervix:	n/a
28	chr5:76108191-76108241	CMK	blood:	n/a
29	chr5:76114812-76114862	HIPEpiC	eye:	n/a
30	chr5:76114933-76114983	HRCEpiC	kidney:	n/a
31	chr5:76119931-76119981	HPAEpiC	pulmonary alveolar:	n/a
32	chr5:76108191-76108241	NB4	blood:	n/a
33	chr5:76114635-76114685	AoSMC	blood vessel:	n/a
34	chr5:76108191-76108241	BJ	skin:	n/a
35	chr5:76116535-76116585	HepG2	liver:	n/a
36	chr5:76114571-76114621	ECC-1	luminal epithelium:	n/a
37	chr5:76115868-76115918	SK-N-MC	brain:	n/a
38	chr5:76115672-76115722	Hepatocyte	liver:	n/a
39	chr5:76114571-76114621	T-47D	breast:	n/a
40	chr5:76114812-76114862	LNCaP	prostate:	n/a
41	chr5:76116169-76116219	NT2-D1	testis:	n/a
42	chr5:76117747-76117797	MCF10A-Er-Src	breast:	n/a
43	chr5:76115309-76115359	K562	blood:	n/a
44	chr5:76114933-76114983	Hepatocyte	liver:	n/a
45	chr5:76117747-76117797	AG04450	lung:	fetal
46	chr5:76114822-76114872	HRE	kidney:	n/a
47	chr5:76112996-76113046	NH-A	brain:	n/a
48	chr5:76119931-76119981	AG09319	gingival:	n/a
49	chr5:76114933-76114983	HepG2	liver:	n/a
50	chr5:76114635-76114685	MCF-7	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:76103612..76107653-chr5:76108707..76113004,3	MCF-7	breast:
2	chr5:76094721..76097053-chr5:76101788..76104241,2	K562	blood:
3	chr19:796813..797729-chr5:76114268..76115162,3	HCT-116	colon:
4	chr5:76123012..76125302-chr5:76125595..76128318,2	MCF-7	breast:
5	chr5:76105222..76108652-chr5:76112389..76115245,3	K562	blood:
6	chr5:76110973..76114089-chr5:76116480..76119427,3	K562	blood:
7	chr5:76094082..76095930-chr5:76098926..76101541,2	K562	blood:
8	chr5:76094082..76095930-chr5:76098926..76101541,2	K562	blood:
9	chr5:76103612..76107653-chr5:76108707..76113004,3	MCF-7	breast:
10	chr5:76115175..76117196-chr5:76160540..76162682,2	MCF-7	breast:
11	chr5:76113078..76116046-chr5:76145704..76148210,2	K562	blood:
12	chr5:76110973..76114089-chr5:76116480..76119427,3	K562	blood:
13	chr5:76123012..76125302-chr5:76125595..76128318,2	MCF-7	breast:
14	chr5:76127088..76128697-chr5:76136604..76139100,2	K562	blood:
15	chr5:76106690..76108652-chr5:76112389..76115245,2	K562	blood:
16	chr5:76115218..76117725-chr5:76325993..76327834,2	MCF-7	breast:
17	chr5:76094721..76097053-chr5:76101788..76104241,2	K562	blood:
18	chr5:76083391..76086055-chr5:76095285..76096948,2	MCF-7	breast:
19	chr5:76101619..76103504-chr5:76111998..76114759,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-S100Z-1	chr5:76114806-76115096	NONHSAT102251

No data

Variant related genes	Relation type
F2RL1	TF binding region
F2RL1	CpG island
ENSG00000171643	chromatin interactions
ENSG00000164252	chromatin interactions
ENSG00000011304	chromatin interactions
ENSG00000164251	chromatin interactions

Extended variants
information (count: 1621 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1621 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs458124	chr5:76090951-76090952	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs369571192	chr5:76091034-76091035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs73131669	chr5:76091102-76091103	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs557371503	chr5:76091103-76091104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs574131726	chr5:76091106-76091107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs192241573	chr5:76091151-76091152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs13170013	chr5:76091163-76091164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs78953091	chr5:76091207-76091208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs559550465	chr5:76091266-76091267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs528591762	chr5:76091268-76091269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs546110546	chr5:76091276-76091277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs540843655	chr5:76091309-76091310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs377496441	chr5:76091328-76091329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs138094762	chr5:76091353-76091354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs374748851	chr5:76091454-76091455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs549690031	chr5:76091461-76091462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs185418136	chr5:76091482-76091483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs528921267	chr5:76091490-76091491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs376113431	chr5:76091491-76091492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs458380	chr5:76091497-76091498	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs142699745	chr5:76091500-76091501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190769921	chr5:76091507-76091508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs534736901	chr5:76091529-76091530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs180786113	chr5:76091540-76091541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs670071	chr5:76091596-76091597	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs138001420	chr5:76091649-76091650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs35199780	chr5:76091667-76091668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs537738233	chr5:76091675-76091676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs78184088	chr5:76091692-76091693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs536030960	chr5:76091694-76091695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs79852526	chr5:76091695-76091696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs184658234	chr5:76091731-76091732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs574286482	chr5:76091739-76091740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs542610127	chr5:76091746-76091747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs111577200	chr5:76091753-76091754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs188498355	chr5:76091757-76091758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs371802832	chr5:76091762-76091763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs73131670	chr5:76091763-76091764	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs143573901	chr5:76091767-76091768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs538388269	chr5:76091801-76091802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs74421478	chr5:76091887-76091888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs563200684	chr5:76091949-76091950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529189998	chr5:76091962-76091963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548674318	chr5:76092022-76092023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs406171	chr5:76092051-76092052	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs77030223	chr5:76092112-76092113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs463466	chr5:76092225-76092226	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs77223652	chr5:76092259-76092260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538909800	chr5:76092279-76092280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs73131671	chr5:76092285-76092286	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	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
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	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
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1245 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:76087600-76094800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr5:76087800-76095800	Weak transcription	Small Intestine	intestine
3	chr5:76088000-76095400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr5:76088000-76097000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr5:76088000-76097000	Weak transcription	NHLF	lung
6	chr5:76088000-76100000	Weak transcription	HepG2	liver
7	chr5:76088200-76096000	Weak transcription	Hela-S3	cervix
8	chr5:76088200-76096600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr5:76088200-76097000	Weak transcription	Fetal Lung	lung
10	chr5:76088200-76097400	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr5:76088200-76101400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr5:76088400-76097000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr5:76089000-76097000	Weak transcription	NH-A	brain
14	chr5:76090000-76091800	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr5:76090200-76091000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr5:76090200-76091000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr5:76090200-76091000	Enhancers	Osteobl	bone
18	chr5:76090200-76091600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr5:76090400-76091000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr5:76090400-76091000	Enhancers	A549	lung
21	chr5:76090400-76091200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr5:76090600-76091000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
23	chr5:76090600-76091200	Enhancers	HMEC	breast
24	chr5:76090600-76091200	Enhancers	NHEK	skin
25	chr5:76090800-76091000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr5:76090800-76091000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr5:76090800-76091000	Enhancers	Fetal Muscle Trunk	muscle
28	chr5:76090800-76091200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr5:76090800-76091200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr5:76090800-76091200	Enhancers	Muscle Satellite Cultured Cells	--
31	chr5:76091000-76091600	Enhancers	Monocytes-CD14+_RO01746	blood
32	chr5:76091000-76094800	Weak transcription	A549	lung
33	chr5:76091000-76095400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr5:76091000-76096800	Weak transcription	Osteobl	bone
35	chr5:76091000-76097000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr5:76091000-76101800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr5:76091200-76095400	Weak transcription	HMEC	breast
38	chr5:76091200-76095400	Weak transcription	NHEK	skin
39	chr5:76091200-76096600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr5:76091600-76095400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr5:76094200-76094800	Weak transcription	Fetal Intestine Small	intestine
42	chr5:76094800-76095000	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr5:76094800-76095400	ZNF genes & repeats	Fetal Intestine Small	intestine
44	chr5:76094800-76097200	Enhancers	A549	lung
45	chr5:76095000-76101400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr5:76095400-76096000	Enhancers	Duodenum Mucosa	Duodenum
47	chr5:76095400-76097800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr5:76095400-76098000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr5:76095400-76098000	Enhancers	NHEK	skin
50	chr5:76095400-76098200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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