| Tag | Content |
|---|
EnhancerAtlas ID | HS129-05570 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr10:115820460-115821900 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr10:115821842-115821858 | AATTAAGTAAATAAAT | + | 6.21 |
|
| | 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 |
| GH10I114060 | chr10 | 115820222 | 115821620 |
|
Enhancer Sequence | GATTATACGA AATGCCACTG AATTGTGAGC TTTAAAATGA CTAAAATGCT GAATTTTATG 60
ATATGTGTCT TTTACCACAA TAAAAAGAAA AATCCTATAG AATTATTTTC TATTAGGCTT 120
GCAATTTGTT TAGCTAAACA AAATCATGTA AAACCAAAAC TGGGGAAGCT ATTTTAATAA 180
AAGAGAAAGG AAGAAAATTA CCGTCACTTG AACAATGGTG AAATATATTT TTATCAGAGT 240
TTAACGCATG CAAGGAGGAA TCTTAGTCTT CATAAGCCAA TGTGATTTCT TCTTTTTACA 300
GATAAAAAAG TTAAGGCTTT TGTGGTAACC CAGTGTTCAG GAACAGACAT CTAGATTTGA 360
GTCTTTCTCT GCCAGATTTA TGGGCTATGC AATTTAAGTG CAGTTACTTG GAGCTCTCCG 420
AAACTCAGTT TCCACATCAG TAAACTGAAA ATATCTAGGG CTGATCTTTT GAAAATATCA 480
TCAGACCTCA TGATTCACCA AAGCCAAATC AATTAGAAGT TACTTCAAGA CGAGAGAATA 540
CCACCATGAC AAAGTCTTAG CAGTGCCTCA TAAGAAGGAA GTCAAAATGG ATATTTATAG 600
GGTTTTAGCT CCTGGGGCAC ATATGATTCA CGGCAGGCCT TTCAAGGTGC AACCGGTTGA 660
GATTGGGCAG GATTTGCAAC ATAATAGTGT AAGATTGGCC GGCTTAGCAG CGCAAAGGTC 720
TTGAAGCAAG TCTTGACAGG TAAACTGTTG TTTGAATAGC AAGCTGCTTG CCTGTTGTCT 780
CAGATAAATT CCTACCGGAA TTTTCTGAAG CAAACTGTGC AGTTATTTAT TGACTTACAG 840
TCTTACTCCT GTTGAGGGAA GGGTTCCTGG AACAAACAAC TAAATTGTGA TAACACCGGT 900
GGTCTCAGTT TCAGTCCTGA GTCTGTCATG TCTGATACAG GTCGGAGTTC CCAGAGATGC 960
TATGGTCACG TGTCAAGCGC ATAGCCTGGG CACTCAATAC ATCCTTCATT TTTTACCAAA 1020
GCATCACCAC CATTTCCGCT CAAAACTTGC TCCTTGATAG TGAATCTCTG TCAGAACTAG 1080
AAGAAAGGTT TGTGCTGTAC AGACCGGAAC CCTTCCTGCC ATCCACAGTC GGACTGGGCT 1140
CCACTTCTTT GGTCAAAGGC AAATTAATTC AGCTACAATA AAGACTCCCA AGTCTTTTCA 1200
CCATCCTGAA TGAGGCAGCA GCAGAGCGCA GGGTTATGAT GCTGACAGAC CGAGGCCCTA 1260
GCTTCCCTGT TGCTTGATTT GTGACCCTAG GCCAGTTATT TCCCTCTTCC AGCCTCACTT 1320
CCTCATCTAG AAGATGAGGA CGATCGCGTT TAGCACGTAA TACATATTCG GCTAACTTTT 1380
TAAATTAAGT AAATAAATTG TTCTCTCAAA TTTTTTTTAA ATTTTTTTTC TAAGGTTGAA 1440
|
