| Tag | Content |
|---|
EnhancerAtlas ID | HS012-26415 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chrX:17613330-17614790 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXC1 | MA0032.2 | chrX:17613959-17613970 | ATATTTACTTA | - | 6.14 | | NR2C2 | MA0504.1 | chrX:17614658-17614673 | CAAGGTCAAAGGTTA | + | 6.25 | | Nr2f6 | MA0677.1 | chrX:17614659-17614673 | AAGGTCAAAGGTTA | + | 7.22 | | Rxra | MA0512.2 | chrX:17614659-17614673 | AAGGTCAAAGGTTA | + | 6.86 |
|
| | 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 |
| GH0XI017593 | chrX | 17611953 | 17615353 |
|
Enhancer Sequence | TGCAAGCTCA TTCTTTGATC CTGAAGAGTG GGTACCAAGC AAGGATCCTT TCCATGAGAC 60
TGATGGTATA GACACTTTCC CTACCCATTC TTTGTGAGCC ATCTGCTGCT GAAGTCCTCC 120
TCTGTCTCAG CTGAGATTTA ATGTGGCAAC ATCTGCCCTA GGGTTTTGAC TTTAATGGCA 180
TTTATCATGC ACACTTCCCT TTGATGTAGG ACAGCCAACC TCATGACATC TTCTGTCTTC 240
TATCTCCAGG TTTTATTTCT CCTCTTAGTT TAGATGTCCC TCATATTCTC TCTAAACTCC 300
TGTCCAACCC TTCCCTCTCA AATCTTGTTA ATACTTAACC TGGGGTCAAG GTTTCTTTGG 360
GCGCAGAACA ATGAAAAGGC AATTAGCTAG CTGGCTTTGA GTGCTAAGGG AGTGAAAACT 420
GGTTATGACT CTAACTTGAG ACATTCCTAA GAGTAGGCCT TTCCTGTATG GTCAAGACTG 480
AAAGAAATAA ACGGATGTGG GCTTTTTTCT TGCCTTTAGA CTTTATGGAT TAGTCATAGG 540
ATCTTGTTGA AATTATTCAG TCCAGAAATA AGTGATTAAC ATTTAACTTC TTTAATGGGC 600
AATTACTCAA CAGCTATGCC AGTGGGTAAA TATTTACTTA TCATCTATTC CAAGGAGTGA 660
ATGTTAACTT GAGTCAAACA GTTACTTGTG TTGGTTCTTT AATAGCGGAA AAGTGAATTT 720
ATATGGCTCT AGGAGTTCCA ATTTCCCACC AAATAAGAAC TTACTGAAGG ATGTTCAGAG 780
CCCTGGGCTG GAGTTAAATT ACAGACAATT TGCTTACCTA CTCCCTCCCT CCAAAAAAAA 840
AAAGATGAAG ATTTTTTGTA CTCACCACTA TTTATTGAAA TCTGGTAGCT TCAAATCTCA 900
CAAAGCCAAA CAAATTCACT CAGTTTTTCA GTCTGTAGGT CTGTGACAGC CTCTGTTTAC 960
CACAAAACTG CCTGTATCTT GTCACTATGG ATGCAAGTCA AGACAGAGGC AAAGTCTGGA 1020
TGATGAATGG CTTGTTCTTA GTAATGTGCT TGTAATTGTT CTTCCTTAGA ATGGGAAGGA 1080
TGGCTTGGGA GGACCTGTCT ATCATAGAGG GACTTGGCAG CTTCCAATCT CTTTGCTTGC 1140
TTGTCTACAA TGCAGCCAAT GGGACTAATT CAAATATCCC AGACATGCCC AGATGGATAC 1200
ACAGAGCATA TGGCTTGAAG ACTCAGTTAT GGAAATAACA GGCACCATTT CTGAGACTTT 1260
CAATTCACTT CCAACAAATA TATTTTAATC AACAGGCAGG AAACCAAATT AAAAGTTGAA 1320
GCATGAACCA AGGTCAAAGG TTAAGGGTTA GGATGTGGGA TTTTGGTGTT CATGCTCCAG 1380
GTTTGGCCTA CCATGCAGAG AGGTCAAAGA TGACTGCACA GGGAACCATT GGGAGAGAGG 1440
AATGTGGTAT TCCAGTTTGT 1460
|
