| Tag | Content |
|---|
EnhancerAtlas ID | HS101-01008 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:31778770-31780130 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr1:31778960-31778972 | GAATGTTTTTTT | + | 6.52 | | Foxq1 | MA0040.1 | chr1:31779380-31779391 | AATTGTTTATT | + | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr1:31779903-31779918 | CGAACTCTTGACCTT | - | 6.06 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 31778951 | 31779748 | | chr1 | 31779048 | 31779636 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I031305 | chr1 | 31778092 | 31780203 |
|
Enhancer Sequence | ATACATTCCA AGACCCCCAT TGGATCCCTA AAATTGTGGG CACTGCTGAA CCCAGTTGCT 60
ATCAATTGGA AGACGTTTCT GTTTGTATTT TCTACCCACA AATTTAATGC CTTCTCCATC 120
TTAACTAAGC ACTTATCATA CACTGTGGCT ATAACTTTAG CAGTTTGAGG TGCAACAGCA 180
AAACTAACAT GAATGTTTTT TTCTTCCTCA CAATTTCAGA CATCGAAGAT TCATTCTTAC 240
TATAGATCTT AGCAACCTTA GCATACAATT TTTTTTTTCC CCTTGAGAAC TTTCACCCTT 300
TCACTTAAAG GAAGCAGTTT ACAGCTTCTC TTTGGTATAC CAAAATTGCC AGCATTACTA 360
CTCTGCTTCG TGGCCATTAT TAAGTAAAGA AAGGATTATT TGAACACAAG CAGAGATACT 420
TCAACAGTCA GTCTGATAAC CAAGATGGCT ACTATGTGAC TAATGGGCAC TTAATATACA 480
CTGAGTGACT AGTGTATGCA GCATGGATAC GCTGGACAAA GGGGATGATT CATATCCCAG 540
ATGGAACAGA GTGGGATGGC ACAAGATTTC ATCACACTAA TAAGAACAAC ATAACAGTTT 600
TAAGCTTATG AATTGTTTAT TTCTGGAATT TTTCATTTGG TGTTTTTGGA CCGTGGTAGA 660
CTGTGAGTAA CTGCAACTGT GGAAAGTACA ACTGTGGATG GGAGGACTAC TGTACTGTTA 720
TATTTCAGGC TTTCCCTCAA AAATGCATGC CAGTTTTTTT TTGAGATAAG GTCTCACTGT 780
GTCGCCCAGG CTGGATTGCA TTGGCATGAT CGTACCTCAC TGCAGCCTTG ATCTCCTTGG 840
CTCAAGCGAT CCTCTTGCTT CAGCCTCCCA AGTAGCTGGG ATTATAGGCT GGTGTCACCA 900
CACCTGGCTG ATTTTTTTTC TTTTTTTCTT TTTGAGACGG AGTCTTGCTC TGTCACCAGG 960
CTAGACTATA GTGGGGCCAT CTCGGCTCAC TGCAGTCTCC GCCTCCCGGG TTCAAGCAAT 1020
TCTCCTGCCT CAGCCTCCCA AGTAGCTGGG ACTACAGGTG CGCACCACCA TGCCTAGCTA 1080
ATTTTTGTAT TTTTAGTAGA GACGGGGTTT CACTATGTTG GCCGGGATGG TCTCGAACTC 1140
TTGACCTTGT GATCCACCCG CCTTGGCCTC CCAAAGCGCT GGGATTACAG GCGTGAGCCA 1200
CTGTGCCTGG CTGATTTTTT TTTTTTTTAA GTAGAGATAG AGTCTCACTG TGTTGTCCAG 1260
GCTGGTCTTG AACTCCTGGC CTCAAGTGAT CCTCCCGCCT TAGCTTCCCA CGATTACAGT 1320
CGTGAGCCAC TGCACCTGGC CCCAGTTTCC TTCTTGAAGA 1360
|
