Variant report

Variant	nsv1021460
Chromosome Location	chr5:76089512-76129241
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1383)
CpG islands
(count:1466)
Chromatin interactive
region (count:19)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1383 , 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	chr5:76126912-76127331	GM12878	blood:	n/a	n/a
8	ATF2	chr5:76103823-76104436	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr5:76113947-76114568	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr5:76126950-76127363	GM12878	blood:	n/a	n/a
11	ATF2	chr5:76103843-76104561	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	chr5:76101627-76102562	A549	lung:	n/a	n/a
14	ATF3	chr5:76114447-76115003	A549	lung:	n/a	chr5:76114977-76114986 chr5:76114862-76114870
15	ATF3	chr5:76100044-76100672	A549	lung:	n/a	n/a
16	ATF3	chr5:76114432-76115010	A549	lung:	n/a	chr5:76114977-76114986 chr5:76114862-76114870
17	ATF3	chr5:76099975-76100655	A549	lung:	n/a	n/a
18	ATF3	chr5:76101689-76102467	A549	lung:	n/a	n/a
19	BACH1	chr5:76114200-76116153	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr5:76103704-76103712	K562	blood:	n/a	n/a
21	BACH1	chr5:76126596-76126774	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	chr5:76126931-76127279	GM12878	blood:	n/a	chr5:76127105-76127114
25	BCL11A	chr5:76126997-76127227	GM12878	blood:	n/a	chr5:76127105-76127114
26	BCL3	chr5:76097061-76097862	A549	lung:	n/a	n/a
27	BCL3	chr5:76126983-76127322	GM12878	blood:	n/a	chr5:76127105-76127114
28	BCL3	chr5:76109782-76110506	A549	lung:	n/a	chr5:76110348-76110357
29	BCL3	chr5:76101997-76102356	GM12878	blood:	n/a	chr5:76102262-76102271
30	BCL3	chr5:76099724-76100840	A549	lung:	n/a	chr5:76100092-76100100 chr5:76100201-76100210
31	BCL3	chr5:76101972-76102349	GM12878	blood:	n/a	chr5:76102262-76102271
32	BCL3	chr5:76126926-76127294	GM12878	blood:	n/a	chr5:76127105-76127114
33	BCL3	chr5:76101399-76102582	A549	lung:	n/a	chr5:76102262-76102271
34	BCL3	chr5:76126569-76127455	A549	lung:	n/a	chr5:76127105-76127114
35	BCL3	chr5:76114082-76115135	A549	lung:	n/a	chr5:76114962-76114971 chr5:76114691-76114704
36	BCL3	chr5:76099974-76100817	A549	lung:	n/a	chr5:76100092-76100100 chr5:76100201-76100210
37	BCL3	chr5:76115978-76116822	A549	lung:	n/a	n/a
38	BCL3	chr5:76109914-76110498	A549	lung:	n/a	chr5:76110348-76110357
39	BCL3	chr5:76101545-76102516	A549	lung:	n/a	chr5:76102262-76102271
40	BCL3	chr5:76126827-76127402	A549	lung:	n/a	chr5:76127105-76127114
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	chr5:76121429-76121600	A549	lung:	n/a	n/a
44	BHLHE40	chr5:76126969-76127195	A549	lung:	n/a	n/a
45	BHLHE40	chr5:76126954-76127367	GM12878	blood:	n/a	n/a
46	BHLHE40	chr5:76090863-76090978	K562	blood:	n/a	n/a
47	BRCA1	chr5:76114112-76114340	H1-hESC	embryonic stem cell:	n/a	n/a
48	BRCA1	chr5:76115005-76115163	H1-hESC	embryonic stem cell:	n/a	n/a
49	BRCA1	chr5:76110002-76110390	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr5:76101731-76102250	Hela-S3	cervix:	n/a	n/a

(count:1466 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:76112996-76113046	MCF10A-Er-Src	breast:	n/a
2	chr5:76112776-76112826	U87	brain:	n/a
3	chr5:76112996-76113046	MCF10A-Er-Src	breast:	n/a
4	chr5:76112776-76112826	U87	brain:	n/a
5	chr5:76115810-76115860	HEEpiC	esophagus:	n/a
6	chr5:76114373-76114423	CMK	blood:	n/a
7	chr5:76112776-76112826	HIPEpiC	eye:	n/a
8	chr5:76115868-76115918	HPAEpiC	pulmonary alveolar:	n/a
9	chr5:76108191-76108241	GM19239	blood:	n/a
10	chr5:76112996-76113046	ProgFib	skin:	n/a
11	chr5:76112776-76112826	NB4	blood:	n/a
12	chr5:76114933-76114983	ovcar-3	ovarian:	n/a
13	chr5:76114812-76114862	HepG2	liver:	n/a
14	chr5:76108729-76108779	NHBE	bronchial:	n/a
15	chr5:76114635-76114685	Hepatocyte	liver:	n/a
16	chr5:76114522-76114572	HCF	heart:	n/a
17	chr5:76117747-76117797	AG09309	skin:	n/a
18	chr5:76116535-76116585	GM12891	blood:	n/a
19	chr5:76117747-76117797	AoSMC	blood vessel:	n/a
20	chr5:76114933-76114983	CMK	blood:	n/a
21	chr5:76114373-76114423	PrEC	prostate:	n/a
22	chr5:76112996-76113046	H1-hESC	embryonic stem cell:	embryo
23	chr5:76114635-76114685	MCF-7	breast:	n/a
24	chr5:76114933-76114983	HRE	kidney:	n/a
25	chr5:76116088-76116138	HRPEpiC	eye:	n/a
26	chr5:76112776-76112826	HRE	kidney:	n/a
27	chr5:76119931-76119981	SK-N-SH_RA	brain:	n/a
28	chr5:76114635-76114685	HCT-116	colon:	n/a
29	chr5:76119931-76119981	HRPEpiC	eye:	n/a
30	chr5:76114933-76114983	NB4	blood:	n/a
31	chr5:76116535-76116585	HCPEpiC	choroid plexus:	n/a
32	chr5:76114684-76114734	AG04450	lung:	fetal
33	chr5:76114373-76114423	HCT-116	colon:	n/a
34	chr5:76119931-76119981	GM12891	blood:	n/a
35	chr5:76114571-76114621	AG04449	skin:	fetal
36	chr5:76116535-76116585	HMEC	breast:	n/a
37	chr5:76119931-76119981	HEEpiC	esophagus:	n/a
38	chr5:76111995-76112045	SK-N-MC	brain:	n/a
39	chr5:76114635-76114685	Caco-2	colon:	n/a
40	chr5:76114822-76114872	HepG2	liver:	n/a
41	chr5:76117747-76117797	HUVEC	blood vessel:	n/a
42	chr5:76114522-76114572	PrEC	prostate:	n/a
43	chr5:76117747-76117797	HRCEpiC	kidney:	n/a
44	chr5:76115810-76115860	SKMC	muscle:	n/a
45	chr5:76114933-76114983	NHBE	bronchial:	n/a
46	chr5:76112776-76112826	AG09309	skin:	n/a
47	chr5:76116169-76116219	AG09309	skin:	n/a
48	chr5:76115672-76115722	ovcar-3	ovarian:	n/a
49	chr5:76108729-76108779	K562	blood:	n/a
50	chr5:76108191-76108241	AoSMC	blood vessel:	n/a

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

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

(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
ENSG00000011304	chromatin interactions
ENSG00000164251	chromatin interactions
ENSG00000164252	chromatin interactions
ENSG00000171643	chromatin interactions

Extended variants
information (count: 1673 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1673 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541975617	chr5:76089514-76089515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs562163334	chr5:76089539-76089540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs150068586	chr5:76089593-76089594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541393273	chr5:76089605-76089606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs552310799	chr5:76089627-76089628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs153307	chr5:76089635-76089636	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs533411429	chr5:76089675-76089676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs542013821	chr5:76089698-76089699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs153308	chr5:76089705-76089706	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs529410037	chr5:76089724-76089725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs548331213	chr5:76089750-76089751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs112946945	chr5:76089812-76089813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs146820270	chr5:76089863-76089864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs368968852	chr5:76089875-76089876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs547423273	chr5:76090004-76090005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs570105425	chr5:76090022-76090023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs182998443	chr5:76090059-76090060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs536273663	chr5:76090076-76090077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs546915367	chr5:76090085-76090086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs371208177	chr5:76090092-76090093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs566814177	chr5:76090112-76090113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs538945706	chr5:76090149-76090150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555746114	chr5:76090192-76090193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs575701721	chr5:76090236-76090237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs73131665	chr5:76090241-76090242	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs555911234	chr5:76090266-76090267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs575420373	chr5:76090307-76090308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs561849673	chr5:76090318-76090319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs115295393	chr5:76090377-76090378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs191941223	chr5:76090388-76090389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs578252423	chr5:76090389-76090390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs140633501	chr5:76090403-76090404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs537934701	chr5:76090484-76090485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs563688801	chr5:76090521-76090522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs201045771	chr5:76090581-76090582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs184501348	chr5:76090592-76090593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs187387987	chr5:76090593-76090594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs527536368	chr5:76090618-76090619	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs460823	chr5:76090621-76090622	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs574736407	chr5:76090628-76090629	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs148041739	chr5:76090638-76090639	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs539372711	chr5:76090653-76090654	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs549328675	chr5:76090666-76090667	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs540660632	chr5:76090717-76090718	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs569343261	chr5:76090754-76090755	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs535509799	chr5:76090763-76090764	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs140875283	chr5:76090765-76090766	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs150171149	chr5:76090836-76090837	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs370174913	chr5:76090855-76090856	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs527511707	chr5:76090889-76090890	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	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:1260 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:76085600-76090400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr5:76087600-76094800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr5:76087800-76090200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr5:76087800-76090800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr5:76087800-76095800	Weak transcription	Small Intestine	intestine
6	chr5:76088000-76090200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr5:76088000-76090800	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr5:76088000-76095400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr5:76088000-76097000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr5:76088000-76097000	Weak transcription	NHLF	lung
11	chr5:76088000-76100000	Weak transcription	HepG2	liver
12	chr5:76088200-76090000	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr5:76088200-76090200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr5:76088200-76090200	Weak transcription	Osteobl	bone
15	chr5:76088200-76090600	Weak transcription	HMEC	breast
16	chr5:76088200-76090600	Weak transcription	NHEK	skin
17	chr5:76088200-76090800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr5:76088200-76096000	Weak transcription	Hela-S3	cervix
19	chr5:76088200-76096600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr5:76088200-76097000	Weak transcription	Fetal Lung	lung
21	chr5:76088200-76097400	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr5:76088200-76101400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr5:76088400-76090000	Weak transcription	Primary monocytes fromperipheralblood	blood
24	chr5:76088400-76090400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr5:76088400-76090400	Weak transcription	A549	lung
26	chr5:76088400-76097000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr5:76089000-76097000	Weak transcription	NH-A	brain
28	chr5:76090000-76090600	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr5:76090000-76091800	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr5:76090200-76091000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr5:76090200-76091000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr5:76090200-76091000	Enhancers	Osteobl	bone
33	chr5:76090200-76091600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr5:76090400-76091000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr5:76090400-76091000	Enhancers	A549	lung
36	chr5:76090400-76091200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr5:76090600-76091000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
38	chr5:76090600-76091200	Enhancers	HMEC	breast
39	chr5:76090600-76091200	Enhancers	NHEK	skin
40	chr5:76090800-76091000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr5:76090800-76091000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr5:76090800-76091000	Enhancers	Fetal Muscle Trunk	muscle
43	chr5:76090800-76091200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr5:76090800-76091200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr5:76090800-76091200	Enhancers	Muscle Satellite Cultured Cells	--
46	chr5:76091000-76091600	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr5:76091000-76094800	Weak transcription	A549	lung
48	chr5:76091000-76095400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr5:76091000-76096800	Weak transcription	Osteobl	bone
50	chr5:76091000-76097000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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