| Tag | Content |
|---|
EnhancerAtlas ID | HS196-02787 |
Organism | Homo sapiens |
Tissue/cell | ZR75-1 |
Coordinate | chr1:178619760-178621140 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr1:178620399-178620414 | TGAGGCCAAAGGTCA | + | 6.59 | | Nr2f6 | MA0677.1 | chr1:178620400-178620414 | GAGGCCAAAGGTCA | + | 6.76 | | Rxra | MA0512.2 | chr1:178620400-178620414 | GAGGCCAAAGGTCA | + | 6.36 |
|
| | 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 |
| GH01I178650 | chr1 | 178619701 | 178623051 |
|
Enhancer Sequence | TTTACCATAT TGGCCAGGCT GGTCTCGAAC TCCTGACCTT GTGATCTGTC CTGCTCTGTC 60
CTGCCTTGGA TTTGAGTCCT CCCTTTGTCC AACATATCCA CGATGTCTAT GCTCCTGCCA 120
TTGGTCACTT AGTAGTTGCA TTGGTTTTCA GATTGACTGT CGGGTCTCAG AGTGCTTGTG 180
TTCAAGTAAC CCTCATTTTA CTTACCTCTT TGCTTAATCA TCCCTATATG TCATCAGTCC 240
CAACTGCAAT GGCAAAAGCT TGTCCTGTTA CCATGGGTTC CCCCAAACAG GCAAGTCCCT 300
TTCCCCCACC ATGGTGGGAC TGAATGAACA ATGCCCTATA GTGATCAGCA TGCACACTCT 360
GAGGGAATTC TGCCCACTTC TGCCACTGCC TGGACTCTGA GAATCGGTGG ACAAGGATCA 420
CAAGGTTGAC TTTTCCTGTT GTTGCTTAGC AGAGTGAATG TTATTTTCTG CTTTGCCATG 480
GCAGTGACCC CTTTAAATGT GGAATTTTTT TTTTCTGTTT GCTCCTCTCT ACTTCTCTGA 540
TTACTCATAG GACAGTAAAA GGATTAACTG AATCCATTCA AAGATGTGTC CTGCTCCAGG 600
CTTCTCTCAG GAAGAGTGCA TGATAAATAT TATATAGCTT GAGGCCAAAG GTCAGCTGAT 660
CCCTCCTCAC AGCTGCCAGA TGGTTGACTC TTCTAGTATA TTCTCAGGGC CACCAGCTCA 720
CTTCCTAGAT ACACATCCCT AAGTCATCTT CCACGCCTCC TGCCTCCAAC CCACTGCGTC 780
CCCAGCCCCA TGTCAAATTG TAACCTTGGA GGCAGCAAGT TCCTTTGCAC GGCAGCTGCT 840
GTGTCAGTTT CTCCTTGACC GATTTACTGT GGCCCTTGAG ACGGCCCCCT TCACAATGTC 900
CTTACTGTTC TTGAGGGCTG AGGAAATCTT TTTCTATGAG TTAAATCCTC CCTACTCATT 960
TAGATGTTTC CTTACAGAAT TTTCAAAACC AGACAGTATG TGTCATACCA TGTTCCCCAA 1020
ATGAAGCTGA AAATCCAATT TATAAGACCA ATTTCTACTC TCTCACAATT TATATTATTA 1080
GGGAAAATGG ATAATAATGA AGCCCACAGA TTTTCACTCC AGAACTGACT TTGCTGCAGA 1140
GGAGTGAGGA GAGCTGCCTG GCAACGCAAC GCATCGCTGT GCATAAACTT TGTTTACAGC 1200
CAAGGCTGGA GTAAAGGAAC AGATGGCAAG AAAATCGGAT TTAAAGAAAG GAAGGATGTG 1260
CTTGCATCTG GGAGCTCGGT AAATCTCTTG GCTTCTGGTG TGCGTACAAG GGTGACGTCT 1320
AGCTACCCCA GCAGTCGCGT CCCAGTTTGC TGTTGATTTT TGCCTGTTTG GATCTGTCTC 1380
|
