| Tag | Content |
|---|
EnhancerAtlas ID | HS047-03613 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr10:5673880-5675170 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOS | MA0476.1 | chr10:5674543-5674554 | AATGAGTCACA | - | 6.62 | | PBX1 | MA0070.1 | chr10:5674499-5674511 | CCATCAATCATT | + | 6.07 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_01811 | chr10:5673277-5675198 | Aorta | | SE_23669 | chr10:5673796-5675183 | Colon_Crypt_1 | | SE_24448 | chr10:5673858-5674404 | Colon_Crypt_2 | | SE_26546 | chr10:5673705-5675274 | Esophagus |
|
| | 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 |
| GH10I005631 | chr10 | 5673239 | 5675871 |
|
Enhancer Sequence | CCATCATTTC TGGCCTTGCA GGGAACACTC TCTCAGCCGT GTTTCCTGAC TGCACTGGGG 60
AGGATTTGGG TCCAAGCTCC TCCTGTAATT TCCTGAGGTC CTGTGAAATG ATCCTGCCCT 120
AGGCAGCTGC GTTCCCAGAG GAGTGTCCAC CTGGGAGCAC GCCACAAGCC CAGAGGAACA 180
TTCTGATTTC CTAATGGAAC CAGATGTCCC AGTTTGGGCA AAAGGGCCTC CCGGGAAAAC 240
AGAGTACTGC CAAGGACTCA GTCTGGCATG TCCCCAGAGG GAGAGAAACT GTCCCCACCC 300
ACCACTTACT TGGATGGAAT TGCTCCCCGG CATGCAGAGG TATCACTGTG TGAGGTCAGC 360
AACGATGCGT GGAGGCCTGT CTCGAGGCGA CCTTCTGGTG GGGAGGACAT TCTCTCCGGT 420
TGTATTTTCA TTCCACTCAG TGTTTCCGTG CAGAGTGGAG TGAGCGCCCC TCCTTGACCT 480
CATGAAGCTG CTCAAGGGCA AAACTCTACC TGGGACTCGA TTTGCTTAGA AACAAAATAC 540
GCAAAGGAAA CACCAATTCA AGGTAGCCTG TTATTCACGG CCAAGAGAGA GACTTCTCTG 600
ACACTTTGGA TCTTTCCCTC CATCAATCAT TTACTTCAGT GCTTGGAATG TCAGGAGGAA 660
AATAATGAGT CACACCTGGT CTGAGGCAAC CAAGTCACTT GTCAGCACAG AGTGCCTGCA 720
ATCACAGCAC TCGGTGACCA AGGCCCAGAT GCTTGGCTGC AGCTGGAGGC ATAACAAGAG 780
GTGCCAGAGA GAAAGACCAG TGAGATACTT TACAGCCAAG ATCTGCAAAG CACACATCCA 840
GGGACTCCAG CTTAGGAAGC CTGGCTGTGA ATGTTTGTTG AATGCAAAGG AACACATCGT 900
TGTAGGCTGG CCTGGGAGCC CAACACAAAA TAAGAATCAG TGCCCAGCTG GGCTTTCAGT 960
TTACTTGTTA TTAGAAATAT TATTGGGCTT TATCAAGTCT TGACAACTCT ATTGCCCTGT 1020
TTGAAAGTGA CACAGAATTA ATCCATGGGC TGTCAGATCA TCTGAGGAAC GGCCTTATAG 1080
ACCAGGCCAG TTTTAGATTC AGCCTGCTGG ATGTGGGAGC CACATGTGGT GGGACAAGCA 1140
CAGGTTGGGG GCTGGATGTG GGAACTCAGT AGCACCCAGC CTCTTGAGTA ATACTGCTCT 1200
CATCAATGCT GTATTTAACC AAAACTGCAC CTAAATCGTA TCTTACCTAT ATTTCTTGAA 1260
TACAAGTTTA TACTCCATGC TATTTTAGAA 1290
|
