| Tag | Content |
|---|
EnhancerAtlas ID | HS193-37174 | Organism | Homo sapiens | Tissue/cell | U87 | Coordinate | chrX:17612960-17614400 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXC1 | MA0032.2 | chrX:17613959-17613970 | ATATTTACTTA | - | 6.14 |
| | | 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 | GGAATTGCAC CACAGAGTTG ATCCCACCTT GAAGTAGGGC ACTGGCCTTT TGTACCATGC 60
TATCAGCCAG TCATTAGCTA TGGGCTGCCT CTGGGAGAGG AGGAATCACC TTCTGAGCTA 120
GATGATTCCC ATTGGCCAAG GGCAATTCTC CAGAGAAGTG AGTTGCTTTT AGCAGCCAAC 180
ACTCATAGCT GGTGGGGAGG AGGATTCCAC CAGAGTTAAG GGGATCTGGG TGGATATCAA 240
CAGCAGCCAC TACACCCACC AAGCTGCTAT ATATGTTCCT GCTGACATGG AATATATGTA 300
GAAGTTCTGT AGGGATTTTG GCTCTTCTCA TTCAGATGCA GGCTGCCTTG CTGGGTGCAG 360
ATAGCTCACC TGCAAGCTCA TTCTTTGATC CTGAAGAGTG GGTACCAAGC AAGGATCCTT 420
TCCATGAGAC TGATGGTATA GACACTTTCC CTACCCATTC TTTGTGAGCC ATCTGCTGCT 480
GAAGTCCTCC TCTGTCTCAG CTGAGATTTA ATGTGGCAAC ATCTGCCCTA GGGTTTTGAC 540
TTTAATGGCA TTTATCATGC ACACTTCCCT TTGATGTAGG ACAGCCAACC TCATGACATC 600
TTCTGTCTTC TATCTCCAGG TTTTATTTCT CCTCTTAGTT TAGATGTCCC TCATATTCTC 660
TCTAAACTCC TGTCCAACCC TTCCCTCTCA AATCTTGTTA ATACTTAACC TGGGGTCAAG 720
GTTTCTTTGG GCGCAGAACA ATGAAAAGGC AATTAGCTAG CTGGCTTTGA GTGCTAAGGG 780
AGTGAAAACT GGTTATGACT CTAACTTGAG ACATTCCTAA GAGTAGGCCT TTCCTGTATG 840
GTCAAGACTG AAAGAAATAA ACGGATGTGG GCTTTTTTCT TGCCTTTAGA CTTTATGGAT 900
TAGTCATAGG ATCTTGTTGA AATTATTCAG TCCAGAAATA AGTGATTAAC ATTTAACTTC 960
TTTAATGGGC AATTACTCAA CAGCTATGCC AGTGGGTAAA TATTTACTTA TCATCTATTC 1020
CAAGGAGTGA ATGTTAACTT GAGTCAAACA GTTACTTGTG TTGGTTCTTT AATAGCGGAA 1080
AAGTGAATTT ATATGGCTCT AGGAGTTCCA ATTTCCCACC AAATAAGAAC TTACTGAAGG 1140
ATGTTCAGAG CCCTGGGCTG GAGTTAAATT ACAGACAATT TGCTTACCTA CTCCCTCCCT 1200
CCAAAAAAAA AAAGATGAAG ATTTTTTGTA CTCACCACTA TTTATTGAAA TCTGGTAGCT 1260
TCAAATCTCA CAAAGCCAAA CAAATTCACT CAGTTTTTCA GTCTGTAGGT CTGTGACAGC 1320
CTCTGTTTAC CACAAAACTG CCTGTATCTT GTCACTATGG ATGCAAGTCA AGACAGAGGC 1380
AAAGTCTGGA TGATGAATGG CTTGTTCTTA GTAATGTGCT TGTAATTGTT CTTCCTTAGA 1440
|
| |
|
|
|
