| Tag | Content |
|---|
EnhancerAtlas ID | HS101-46952 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chrX:41271080-41272370 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chrX:41271905-41271923 | GGAAAGAGACAAGGAAGG | + | 6.03 | | HNF4G | MA0484.1 | chrX:41271696-41271711 | GAAGAACAAAGTTCA | + | 6 | | HSF1 | MA0486.2 | chrX:41271548-41271561 | GAAGGTTCTAGAA | - | 7.12 | | Zfx | MA0146.2 | chrX:41271159-41271173 | GAGGCCGAGGCCGG | - | 6.28 |
|
| | 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 |
| GH0XI041411 | chrX | 41271181 | 41272493 |
|
Enhancer Sequence | AAGAAAAGAA AAAGAAAAAA AAAGAAAAGC TTCAAGAGGT CGGGTGTGGT GGCTCACGCC 60
TATAATCCCA GCACTTTGGG AGGCCGAGGC CGGTGGATCA CTTGAGTCCA GGAATTCGAG 120
ACCAGCCTGG CCAACATGGT GAAACCCCAT CTCTATTAAA AATACAAAAA TTAGCCGGGT 180
GTCATGGCAC GCACCTGTAA TCCCAGCTAC TTGGGAGGCT GAGGCACAAG AATCGCTTGA 240
ACCTGGGAAG TAGAGGTTAC AGTGAGCCGA GATCGCACCA CTGCAGTTCA GCCTGGGCGG 300
CAGATCAAGA CACCGTCTCA AAACAAAACA AAACAAAACA ACTTCAAGAA TAATCAAAAT 360
CAGCTTCATT CACAGGCTCA CAGGGTAGAA GACCAAGAGT CACCTTCCCT AAGTGAGAAG 420
TCCTCTGCAG ATTTTGCATT GGTAGGCAAT CTCAGCTTCT TGCACAGAGA AGGTTCTAGA 480
ATCTCCCTAA GCATGGGGGT GGGGGCAGGA GATGTGATGG GGCACACCCT TATGAAGCGG 540
AGAACTTGCC AGCTGCTGAA ATAGAATAGA GTTCAGAGCT GAAAAGGGCA GGGAGGGTGG 600
AGACACCTGG CTACCAGAAG AACAAAGTTC AGTCCAAGCC CAATTGTCCT TTCCTGGCCA 660
GCTGCCAACC TGCTAGCCTA GGCATTCTAA ACTTTAACAT TTAGTAAAAT GGTCTCAAAT 720
TGGAGAGAGA GTGTCTCTTC TCCTGGAGGA GTGGAAAATG ATGTTGTTCA GTCAGGCCGA 780
GGTTAGCAAC GTTAGCAAAG CCCTCTCTGT CCCTACCTGG TGGCAGGAAA GAGACAAGGA 840
AGGTCTCAAA GATGGATGCC TTGCTACCTT CCTGCAGGCT TTGGGTCAGG TTTGGCTAAG 900
CTATCATTAG CTGTTTCCTG GTTGATATTC AGCTGTAGCC GTGGTGGCAC TTCCTACACA 960
AGCACTGATT TTTCCTCATG TTTGTAAAAC CGGGGCAAAA CTTGGTAAAC TTACTCTTGC 1020
CAAAGTTCTG GATGCTTACT TCCCTTTTGA ATTCTTTTTT TTTTTTTTTT TTGAATCTCA 1080
CTCTGTAGCC CAGGCTGGAG TGCAATGGCG CAATCTCAGC TTACTGCAAC CTCTGTCTCC 1140
CAGGTTCAAG CAATTCTGCT GCCTCAGCCT CCCAAGTAAC TGGGCGCCCG CCACCACACC 1200
TGGCTAATTT TTTGTATTTT AATTTTAATT TAATTTTATT TTTTGAGACG GAGTCTCGCT 1260
CTTGTTGCTG GAGTGCAATG GCAAGGTCTC 1290
|
