| Tag | Content |
|---|
EnhancerAtlas ID | HS193-09762 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr13:114616360-114618020 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr13:114617698-114617711 | GAACCTTCTGGAA | - | 6.15 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH13I113914 | chr13 | 114616101 | 114616654 | | GH13I113913 | chr13 | 114616919 | 114617562 |
|
Enhancer Sequence | TATAAATTTT ATGTGTAGTG GCTCTGGATT CTATTTCTCC AGAAAGTGTT GACAATTTTT 60
GCTTTAGCAG GCAATCACCT TCCTCAAGAG AGGAAGTTTC TAAACCAAGG CGAGTGGTCT 120
GCAGAGCAAA ATCAAGGCAG GCAGACCTCC TCCATCCAAG AGGGCTCTTG GCTTCACTTA 180
GGAGAGATTC ACACACACAC ACCGACAGTG GAGGAAGCGT TGATCAGGAG TGATTCACAC 240
ATGAGCCAAC AGTGGAGGAG GCATTGATCA GGAGTGATTC ACACATGAGC CAACAGTGGA 300
GGAGGCATTG ATCAGGAGTG ATTCACACGT GAGCCAACAG TGGAGGAGGC ATTGATCAGG 360
AGTGATTCAC ACGTGAGCCG ACAGTGGAGG AGGCATTGAT CGGGAGATGA TTCACACGTG 420
AGCCGACAGT GGAGGAGGCA TTGATCGGGA GATGATTCAC ACGTGAGCCG ACAGTGGAGG 480
AGGCATTGAT CGGGAGATGA TTCACACGTG AGCCGACAGT GGAGGAGGCA TTGATCGGGA 540
GATGAATCAC ACGTGAGCCG ACGGTGGAGG AGGCATTGAT CGGGAGATGA ATCACACGTG 600
AGCCGACGGT GGAGGAGGCA TTGATCGGGA GATGATTCAC ACGTGAGCCA ACGGTGGAGG 660
AGGCATTGAT CAGGAGAGAT TCACACGTGA GCCGACGGTG GAGGAGGCAT TGATCAGGAG 720
AGATTCACGC GTGAGCCAAC AGTGGAGGAT GCATTGATCA GGAGATGATT CACACATGAG 780
CCAACAGTGG AGGAGGCATT GATCAGGAGA GATTCACACA TGAGCCAACG GTGGAGGAGA 840
CATTGATCAG GAGTGATTCA CATGTGAGCC AACAGTGGAG GAAGCATTGA TCAGGAGATG 900
ATTCACACAT GAACCAACAG TGAAGGAGGC ATTGATCAGG AGATGATTCA CACATGAGCC 960
GACAGTGGAG GAGGCATTGA TCAGGAGAGA TTCACACATG AGCCGACGGT GGAGGAGGCA 1020
TTGATCAGGA GTGATTCACA CGTGAGCCAA CAGTGGAGGA GGCGTTGATC AGGAGAGATT 1080
CACGCCTGAG CTGACGGTGG AGGAAGCGTT CATCAGGAGA GATTCGCACG TGAGCTGACA 1140
GTGGAGGAGG CGTTGATCAG GAGAGATTCA CACAGAATCA GACAGTGGAA GAAGCATTGA 1200
TTAGGGCGAC AGGGCACAGC CAAAGGCTGC TGCACGGACA GAGCAGGGCT GTCCACTGGC 1260
AAAGGGGCCC CCTCAGATTG CTGGCTGGCT GTTTATACCT CCACCTAATT ACACGTAAAT 1320
GAGGGGTGGG TTATTCACGA ACCTTCTGGA AAGCGGTGTG GAGGTCATGC GGTCCTGGTA 1380
ACACAGGCTG CTTCCTTTTC AGTGACCAGC GTCATTTGGC GCAGCCCCCA GAGTCTCATG 1440
ACAACGACCT TGTTCTGCTC AAGAGCCCTG TACGGTCCCC TCTTCTGTGG ATGGAAACTG 1500
AGGCACAGCA ATGACAGCAT CAACGGAGCC ACCCTGCTCC TGGCTGTGCT CTGCAGGAGC 1560
CTCCACTCGG GGGCAGAGGA CAAACAGCCC CACACTTGGA AGCACAGCTC GGGAGCAGCA 1620
GCTGAGTTGC GCTGTGAGGA GATGCCAGGC GGCTGTTTAT 1660
|
