Tag | Content |
---|
EnhancerAtlas ID | HS133-01903 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:94031490-94032830 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
STAT3 | MA0144.2 | chr1:94031873-94031884 | TTTCTGGGAAG | + | 6.02 |
|
| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_00285 | chr1:94030383-94033619 | Adipose_Nuclei | SE_29507 | chr1:94031300-94034206 | Fetal_Intestine_Large | SE_30459 | chr1:94030837-94032465 | Fetal_Muscle | SE_31653 | chr1:94031457-94031952 | Gastric | SE_45907 | chr1:94030745-94033635 | Osteoblasts | SE_51412 | chr1:94030522-94034040 | Skeletal_Muscle | SE_65777 | chr1:94031886-94032740 | Pancreatic_islets |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I093565 | chr1 | 94030962 | 94034005 |
|
Enhancer Sequence | TGACTGCCTT GGCAAAGCCC TCCTTCCTGA ATGGTCTTTC TGCCAGCAAA CCTTCAGCCT 60 TCCAGCCTTC CTCCACACAG ACACCAGAGT AATTTACTTT AAAACAGAAA TCTGACCATG 120 TGACACCCTC CCATGATTAA ACCCTTCACT GGCTCTTCTT CAGCCACGGT CTTATGTGGA 180 AGGGCTTCCC AGCTGCACCT CCCTCTGTAG CCTAGTTGGC CATTCCTTAG GTCATACTTT 240 GCACAAATCT AAACCCAAGT ACTTGTGGAT CCCAGTTTTC CCCAAGGTCT CTCAGCGCCT 300 TTGCTTGGGT TGTGCCATCT GAGTGGAATT CCCAGCCCTG CTTGCTGGTA ACTGCTTTTG 360 TCCTTTAACA ATCAATGCAG TGTTTTCTGG GAAGCTGTCA CCAGGTGCTT CCTCTTTCCT 420 AACATCTCTG ACCAAATCAG TCCCTTCCCC TAAGTGCTCC CACAGTATAC ACTGCATTTA 480 TCGTACCTGC TTAAATTCCT CAGGACATCC AGTTAGCACG GTGCCGCGCG CATGCCACAT 540 GTGTGATAAA TGCCGGCCGT GCTGACTGAG GAGGCTGCTT TCTGTCACCA TAGCACTTGT 600 AAGAAAAATC CGTTTACGCA ACACTGCCCC ACACTTTCCA GGATGTGTCT GATGCTAAGA 660 GCAGGGGAGC TCACTTCCCA GTGTGACTGG GAAGGAACAG GAATGCAGAT AAATGAGGTC 720 TGGATAAAAC TCCACCTCCT CATCTTGGCA CATCACCTTT TCTAATCTCA CCTATTAGAG 780 GTACTATTAA TAAGTGGTAG GCAAGTTGGC CAATTCTTGT TCTGTTGCCC AGCGCCCAGG 840 CTGGAGTGCA GTGGTGCGAT CTCGGCTCAC TGCAACCTCC GCCTCCCGGG TTCAAGTGAT 900 TCTCCTGCCT CAGCCTCCTG AGTAGCTGGG ATCACAGGCA CACACCATCA CGCCCAGCTA 960 ATTTTTGTAT TTCTATTAGA GACAGGGTTT CATCATGTTG GCCAAGCTGG TCTTGAACTC 1020 CTGACTTCAA GTGATCTACC TGCCTCAGCC TCCCAGAGTG CTGGGATTAC AGGCTTGAAC 1080 CACCACGCCC GGCCCCAGTT CTTTCTTGAC CCCTTCTCTC TGTTTATTCT ATACCATTGA 1140 ACAACAGAAC ACACAAGGAG AAACAGGGCA CTTGAGTCAT TCTGGAATTA AGAGGAAGTA 1200 ATAACTAGCC ATATAGGAAA TGGAATTCCA TTCTTTAATC CTTCCTTTTT GGTCTTTTTC 1260 TAAGTGAAGT CAGCCATGCT CTTCCATTCC TTCATTTCAA TTACGATACA GTGTTAGAGA 1320 ACAGCTTACA AAACCCATCT 1340
|