Variant report

Variant	nsv1025061
Chromosome Location	chr5:76087544-76129241
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1400)
CpG islands
(count:1468)
Chromatin interactive
region (count:19)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1400 , 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	chr5:76114553-76114860	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:76116209-76116734	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:76113989-76114292	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:76101782-76102245	K562	blood:	n/a	n/a
5	ARID3A	chr5:76126576-76126776	K562	blood:	n/a	n/a
6	ATF1	chr5:76101722-76102174	K562	blood:	n/a	n/a
7	ATF2	chr5:76113947-76114568	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr5:76114079-76115052	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr5:76126912-76127331	GM12878	blood:	n/a	n/a
10	ATF2	chr5:76103843-76104561	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr5:76126950-76127363	GM12878	blood:	n/a	n/a
12	ATF2	chr5:76103823-76104436	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr5:76114447-76115003	A549	lung:	n/a	chr5:76114977-76114986 chr5:76114862-76114870
14	ATF3	chr5:76101689-76102467	A549	lung:	n/a	n/a
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	chr5:76101627-76102562	A549	lung:	n/a	n/a
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	chr5:76126956-76127325	GM12878	blood:	n/a	n/a
23	BATF	chr5:76102000-76102358	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	chr5:76099974-76100817	A549	lung:	n/a	chr5:76100092-76100100 chr5:76100201-76100210
27	BCL3	chr5:76114082-76115135	A549	lung:	n/a	chr5:76114962-76114971 chr5:76114691-76114704
28	BCL3	chr5:76099724-76100840	A549	lung:	n/a	chr5:76100092-76100100 chr5:76100201-76100210
29	BCL3	chr5:76126827-76127402	A549	lung:	n/a	chr5:76127105-76127114
30	BCL3	chr5:76101545-76102516	A549	lung:	n/a	chr5:76102262-76102271
31	BCL3	chr5:76115978-76116822	A549	lung:	n/a	n/a
32	BCL3	chr5:76101997-76102356	GM12878	blood:	n/a	chr5:76102262-76102271
33	BCL3	chr5:76109782-76110506	A549	lung:	n/a	chr5:76110348-76110357
34	BCL3	chr5:76101399-76102582	A549	lung:	n/a	chr5:76102262-76102271
35	BCL3	chr5:76109914-76110498	A549	lung:	n/a	chr5:76110348-76110357
36	BCL3	chr5:76101972-76102349	GM12878	blood:	n/a	chr5:76102262-76102271
37	BCL3	chr5:76126569-76127455	A549	lung:	n/a	chr5:76127105-76127114
38	BCL3	chr5:76126983-76127322	GM12878	blood:	n/a	chr5:76127105-76127114
39	BCL3	chr5:76097061-76097862	A549	lung:	n/a	n/a
40	BCL3	chr5:76126926-76127294	GM12878	blood:	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	chr5:76126969-76127195	A549	lung:	n/a	n/a
44	BHLHE40	chr5:76090863-76090978	K562	blood:	n/a	n/a
45	BHLHE40	chr5:76121429-76121600	A549	lung:	n/a	n/a
46	BHLHE40	chr5:76126954-76127367	GM12878	blood:	n/a	n/a
47	BRCA1	chr5:76115005-76115163	H1-hESC	embryonic stem cell:	n/a	n/a
48	BRCA1	chr5:76101731-76102250	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr5:76110002-76110390	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr5:76114112-76114340	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	chr5:76114522-76114572	SK-N-MC	brain:	n/a
2	chr5:76115672-76115722	HepG2	liver:	n/a
3	chr5:76115810-76115860	GM12892	blood:	n/a
4	chr5:76114522-76114572	AG04449	skin:	fetal
5	chr5:76114522-76114572	SK-N-MC	brain:	n/a
6	chr5:76115672-76115722	HepG2	liver:	n/a
7	chr5:76115810-76115860	GM12892	blood:	n/a
8	chr5:76114522-76114572	AG04449	skin:	fetal
9	chr5:76114684-76114734	HCT-116	colon:	n/a
10	chr5:76114571-76114621	GM06990	blood:	n/a
11	chr5:76112776-76112826	GM12878	blood:	n/a
12	chr5:76114822-76114872	CMK	blood:	n/a
13	chr5:76117747-76117797	ovcar-3	ovarian:	n/a
14	chr5:76116169-76116219	NH-A	brain:	n/a
15	chr5:76114933-76114983	LNCaP	prostate:	n/a
16	chr5:76115974-76116024	HCF	heart:	n/a
17	chr5:76117747-76117797	SAEC	small airway:	n/a
18	chr5:76114684-76114734	HRE	kidney:	n/a
19	chr5:76114522-76114572	K562	blood:	n/a
20	chr5:76115810-76115860	MCF10A-Er-Src	breast:	n/a
21	chr5:76112996-76113046	H1-hESC	embryonic stem cell:	embryo
22	chr5:76115974-76116024	MCF-7	breast:	n/a
23	chr5:76119931-76119981	MCF10A-Er-Src	breast:	n/a
24	chr5:76114646-76114696	AG10803	skin:	n/a
25	chr5:76111995-76112045	HRCEpiC	kidney:	n/a
26	chr5:76115672-76115722	Caco-2	colon:	n/a
27	chr5:76114571-76114621	SK-N-MC	brain:	n/a
28	chr5:76115672-76115722	HUVEC	blood vessel:	n/a
29	chr5:76114812-76114862	NB4	blood:	n/a
30	chr5:76114522-76114572	Hela-S3	cervix:	n/a
31	chr5:76119931-76119981	T-47D	breast:	n/a
32	chr5:76112996-76113046	HIPEpiC	eye:	n/a
33	chr5:76114635-76114685	HCF	heart:	n/a
34	chr5:76108729-76108779	HUVEC	blood vessel:	n/a
35	chr5:76119931-76119981	PANC-1	pancreas:	n/a
36	chr5:76108729-76108779	A549	lung:	n/a
37	chr5:76116535-76116585	A549	lung:	n/a
38	chr5:76119931-76119981	K562	blood:	n/a
39	chr5:76115810-76115860	AG09319	gingival:	n/a
40	chr5:76114373-76114423	HAEpiC	amniotic membrane:	n/a
41	chr5:76119931-76119981	HUVEC	blood vessel:	n/a
42	chr5:76116169-76116219	H1-hESC	embryonic stem cell:	embryo
43	chr5:76119931-76119981	SK-N-SH_RA	brain:	n/a
44	chr5:76114812-76114862	NHBE	bronchial:	n/a
45	chr5:76111995-76112045	HRPEpiC	eye:	n/a
46	chr5:76112996-76113046	T-47D	breast:	n/a
47	chr5:76114684-76114734	Hepatocyte	liver:	n/a
48	chr5:76111995-76112045	HCM	heart:	n/a
49	chr5:76114522-76114572	SKMC	muscle:	n/a
50	chr5:76112776-76112826	HCF	heart:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:796813..797729-chr5:76114268..76115162,3	HCT-116	colon:
2	chr5:76094721..76097053-chr5:76101788..76104241,2	K562	blood:
3	chr5:76110973..76114089-chr5:76116480..76119427,3	K562	blood:
4	chr5:76110973..76114089-chr5:76116480..76119427,3	K562	blood:
5	chr5:76094721..76097053-chr5:76101788..76104241,2	K562	blood:
6	chr5:76113078..76116046-chr5:76145704..76148210,2	K562	blood:
7	chr5:76123012..76125302-chr5:76125595..76128318,2	MCF-7	breast:
8	chr5:76101619..76103504-chr5:76111998..76114759,2	K562	blood:
9	chr5:76106690..76108652-chr5:76112389..76115245,2	K562	blood:
10	chr5:76115175..76117196-chr5:76160540..76162682,2	MCF-7	breast:
11	chr5:76105222..76108652-chr5:76112389..76115245,3	K562	blood:
12	chr5:76094082..76095930-chr5:76098926..76101541,2	K562	blood:
13	chr5:76127088..76128697-chr5:76136604..76139100,2	K562	blood:
14	chr5:76094082..76095930-chr5:76098926..76101541,2	K562	blood:
15	chr5:76123012..76125302-chr5:76125595..76128318,2	MCF-7	breast:
16	chr5:76103612..76107653-chr5:76108707..76113004,3	MCF-7	breast:
17	chr5:76083391..76086055-chr5:76095285..76096948,2	MCF-7	breast:
18	chr5:76103612..76107653-chr5:76108707..76113004,3	MCF-7	breast:
19	chr5:76115218..76117725-chr5:76325993..76327834,2	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: 1759 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1759 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114379267	chr5:76087585-76087586	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs574564789	chr5:76087587-76087588	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs534316418	chr5:76087612-76087613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs552878547	chr5:76087694-76087695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs532593864	chr5:76087710-76087711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs58911776	chr5:76087818-76087819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs148918224	chr5:76087850-76087851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs565220298	chr5:76087884-76087885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs192105480	chr5:76087907-76087908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs115902198	chr5:76087965-76087966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs143650399	chr5:76087974-76087975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs151048539	chr5:76088020-76088021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs546708684	chr5:76088041-76088042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs537158419	chr5:76088043-76088044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs73131653	chr5:76088067-76088068	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs566768774	chr5:76088068-76088069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532786805	chr5:76088074-76088075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs552442926	chr5:76088106-76088107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs569161694	chr5:76088143-76088144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs116256911	chr5:76088218-76088219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs548144600	chr5:76088248-76088249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs184645904	chr5:76088346-76088347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs528122194	chr5:76088449-76088450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs397998210	chr5:76088469-76088470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs189456324	chr5:76088515-76088516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs554290771	chr5:76088521-76088522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs182057876	chr5:76088522-76088523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs187432139	chr5:76088538-76088539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs138649902	chr5:76088545-76088546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs567276131	chr5:76088546-76088547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs575579470	chr5:76088551-76088552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs189054680	chr5:76088598-76088599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs376162065	chr5:76088614-76088615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs180967450	chr5:76088619-76088620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs571466822	chr5:76088627-76088628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539947572	chr5:76088676-76088677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs560232857	chr5:76088683-76088684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs11954982	chr5:76088689-76088690	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs545961337	chr5:76088692-76088693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs550508299	chr5:76088697-76088698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs562758245	chr5:76088698-76088699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs113687199	chr5:76088716-76088717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs28786545	chr5:76088747-76088748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs112321157	chr5:76088782-76088783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs376882653	chr5:76088799-76088800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs547486304	chr5:76088826-76088827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs11948340	chr5:76088861-76088862	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs117963428	chr5:76088898-76088899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs558748620	chr5:76088916-76088917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs576229181	chr5:76088918-76088919	Weak transcription Enhancers	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:1334 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:76081600-76088800	Enhancers	Stomach Mucosa	stomach
2	chr5:76083000-76087800	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr5:76083400-76089200	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr5:76084000-76088200	Enhancers	Fetal Lung	lung
5	chr5:76084200-76088200	Enhancers	Fetal Stomach	stomach
6	chr5:76084200-76088400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr5:76085200-76087600	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr5:76085200-76088000	Enhancers	NHLF	lung
9	chr5:76085400-76087800	Enhancers	Sigmoid Colon	Sigmoid Colon
10	chr5:76085400-76088000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr5:76085400-76088000	Enhancers	Adipose Nuclei	Adipose
12	chr5:76085400-76088000	Enhancers	Spleen	Spleen
13	chr5:76085400-76088200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr5:76085400-76088200	Enhancers	HMEC	breast
15	chr5:76085600-76087800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr5:76085600-76088000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr5:76085600-76088000	Enhancers	Brain Hippocampus Middle	brain
18	chr5:76085600-76088200	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr5:76085600-76088200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr5:76085600-76088400	Enhancers	Fetal Muscle Leg	muscle
21	chr5:76085600-76090400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr5:76085800-76087800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr5:76085800-76087800	Enhancers	Fetal Intestine Small	intestine
24	chr5:76085800-76087800	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr5:76085800-76087800	Enhancers	Small Intestine	intestine
26	chr5:76085800-76088000	Enhancers	Duodenum Mucosa	Duodenum
27	chr5:76085800-76088200	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr5:76085800-76088800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr5:76086000-76087600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
30	chr5:76086000-76087600	Enhancers	Primary T helper cells PMA-I stimulated	--
31	chr5:76086000-76087800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr5:76086000-76087800	Enhancers	HSMMtube	muscle
33	chr5:76086000-76088000	Enhancers	HepG2	liver
34	chr5:76086000-76088200	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr5:76086000-76088400	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr5:76086200-76087600	Enhancers	Primary T cells from cord blood	blood
37	chr5:76086200-76087600	Enhancers	Brain Anterior Caudate	brain
38	chr5:76086200-76087600	Weak transcription	Lung	lung
39	chr5:76086200-76087800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr5:76086200-76087800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr5:76086200-76088400	Enhancers	HUVEC	blood vessel
42	chr5:76086400-76087800	Enhancers	Brain Cingulate Gyrus	brain
43	chr5:76086600-76087600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr5:76086600-76087600	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr5:76086600-76087800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr5:76086600-76087800	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr5:76086600-76087800	Enhancers	Fetal Thymus	thymus
48	chr5:76086600-76087800	Enhancers	Ovary	ovary
49	chr5:76086600-76088000	Enhancers	Brain Angular Gyrus	brain
50	chr5:76086600-76088000	Enhancers	Brain Inferior Temporal Lobe	brain

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