| Tag | Content |
|---|
EnhancerAtlas ID | HS184-23994 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr5:55911550-55913040 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr5:55912021-55912042 | GGTCTGTTTCTGTTTCTCTTT | + | 6.43 | | RARA(var.2) | MA0730.1 | chr5:55911800-55911817 | TGACCTTTGGTTGACCT | - | 9.19 | | RREB1 | MA0073.1 | chr5:55912859-55912879 | CCCCAACACACACACACACA | + | 7.29 |
|
| | 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 |
| GH05I056615 | chr5 | 55911428 | 55912627 |
|
Enhancer Sequence | TCAGGAATGT CTTTATAAAA ACTTTGATAT GGTCTAAATT AGGTTTCAAG AAGGAAGGGC 60
AGCCGTGGGA GCAGGAGCCT TTTTCAGTAT TTAACTTTAT GTCCTGACCA GTGCCTAACA 120
CCACTTCATA AATCACAGGT ACCTTGGACT TAGAATGCAC AAGCCCTGTT TCCATGGCCT 180
CGATTTCAGC AGGGACAGAT ACTGCCTGGA GAGAGAGCTT GCCAACCTTC TGTTTTAAGC 240
ACTGCATGTG TGACCTTTGG TTGACCTTAG GTTCTGGGAT TTGAGGGTTA AAGTTGTCTT 300
TTGGCACTGG AGCCTGATTT TTTTTTTTTC TCCAAAAGTG TTTAGAGAAA TAAGAGAGCG 360
CCCCACCCTC TGCAGCAGGG CAAGCTGTTT CCTGTAGAAG CAAGAGTTAG TGGCTATCCC 420
AGTTATTCCT TGTAAAAAAT ACTTCTTCAG GAGAAAAACT CTTTCTCAAG GGGTCTGTTT 480
CTGTTTCTCT TTCAATGCCT AACTCTCCAA GGAGTTTACT TAGAATTAGC ATGGTCTTTG 540
CATAAAGGCG GACAAAGCAA AGGCGATGCT GTTTGTTTTC AAGGTGAGAA TTAGACCAAA 600
ACAAGAATCT GACAGGTTGA ACCAAATGAA AAGCCCTCAC TTCTCTGAAC ATGAATTTTC 660
TTTGCACAGA TTGTTTTTTC CTGAAGGCAG ATCACTGAGG GGCAGGTGGA TTATAGGAAC 720
CTAAACTACA TAATCGTCTC TAATAAATGA ACATTTTTAC CGCACCAACG GTTGATTAGG 780
GATATACCAC GAAACATACT AGCCTATTTC TGAGTGAAGC AGGAAAGCTT TCATAGAGAG 840
GTTTTATTGT TTACATTCAA TGAAAGGAAA AGTCTGACTT GAAGTAGTCA GATATAATCT 900
CTCTCTGAAT TAAAAGGGTT CTATTGTACT AAGATGCTGG TGCTGTTAGC AAAGGTGAAT 960
CCAGGATTTT TGCCCAGGCA CAGAATGCCT TTATACAAGC GAGCTATACA TGTGGCCACA 1020
AACAGACAAA CTTGCCTGGT TATTGGCAGC CATTCTCAGT GTAAGAAGAG TTTATTTTCC 1080
TTTAGGAGCC CACAGTTGAA CAATGTTCTG GTGCCCTAGC TGTTTCATAA CTTTCCATGT 1140
AATTAAGCAG TTGGCATGAC CTTCTGTAGC AAGATAATAA TAGGAATTAG CAAAGGCGGG 1200
GCTTGTACAC AAGGACACTT TGGACTACTC AAGCTCACAA ATAAAAGCTT TCAAATAAAT 1260
GCAAAACTGT CTTTCAAATT CAAAGAGCTT TCCTAGTGAA GTGACACTCC CCCAACACAC 1320
ACACACACAA ACACACACAC ACACACACAC ACACACTGCA AGCAAACATG ACAAAATTTC 1380
CTGTAACTTG AGAACTGCAA GGGACAATTC AAAAAGGTGG GAGGAAGCAG ACCTGGTCAT 1440
CATTTTTCAA AAGCCACCTT CACTGTCTAG ATGAACTTAA GGATGAATAT 1490
|
