Tag | Content |
---|
EnhancerAtlas ID | HS012-12496 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr13:30415530-30417050 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr13:30416261-30416282 | ATTCTCTTTCTTTTTTTTTTT | + | 6.22 | LMX1B | MA0703.2 | chr13:30415648-30415659 | TTAATTAAAAT | - | 6.62 | ZBTB18 | MA0698.1 | chr13:30415665-30415678 | AATCCAGATGTTA | + | 6.24 |
|
| 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 |
GH13I029841 | chr13 | 30415241 | 30416916 |
|
Enhancer Sequence | AGTAGTACTT TTTAAGAAAA ATCCACTGTG TAACAAATAT ATACATAAGA AGACTCAAAG 60 TTCCAACAAG TTTAAAGGAA ACTCCCTTTA ATTTTACCAA TTAGTAAGAC AACCAACCTT 120 AATTAAAATC ATTCCAATCC AGATGTTACA TAGTTTATTA CAAAGATATA TGAAGTAGGT 180 TTCATTTCTA CCATGCTAGC TCAGACCAAT CAGTAGGGAC TCCCTGGAGC AAGGTATTGG 240 GAAGGAATCT AAGGCATTCT TAGGATAATG TGCCTGAGGG ATTCAGTAAT GTTTGCTCAG 300 TTACCGTTGT GGGGAGGGGT GTAGATGTTT ATCACTATTG CCACCAGACC CAAACTCCTA 360 TTCTAGCTCA ACTTCTTCCT CGCTATGTGA TCTCAAACAA GTTCCTTACC CTCTCTGAAC 420 CTAGGCTGTG AGAAAGTAAA AATGAGCTCG GTTGATAATC AGACTGTGAT ATCTGAAAGA 480 TAGAAGACCA ACAGGTAAAA AGTTTTTCCT ATGGCCACAC TGCAGCTCCA AAATGACCAA 540 CAATCTCCCA TTCTGTAAGT GATTATGTTT TCTCACCAAT GACTTTCCAA ATCCCCTTCA 600 TTTATCCTGT CTCCTAAACA AAGACTGCTG AAAGACCCAA TTACTAACCC ACCTCCAGTT 660 GATGTACGAT AGCATTCAGT CCAGGAGTCC CTGCTTCCAG CACAGCCCAA ACCCTACTGA 720 AAACTCCTCC CATTCTCTTT CTTTTTTTTT TTTTTTTTTT TTTTTAGAGA CAGAGTCTTA 780 CTCTGTCGCC CAGGCTGGAG TGCAGTGGCG CAATCTCAGC TCACTGCAAC CTCTGCTCAC 840 TGCAACCTCC ACCTCCTGGG TTCAAGTGAT TCTCCTGCCT CAGCCTCCGG AGTAGCTGCG 900 ATTACAGACG CCTGCCACAA TGCCCAGCTA ATTTTTGTAT TTTTAGTAGA GATGGGGGTT 960 TCACCATGTT GGTCAGGGTG GTCTCGAACT CCTGACCTCA AGTGATCCAC CCACCTCGGC 1020 CTCCCAAAAT GTTGGGATTA CAGGTGTGAG CCACCGTGCC CAGCCCTCCC ATTCTCTTTT 1080 ACTGACACTT GGCAGGATCT GGCATACGCT CTTCCTAGCT GCAAAACAGT CAACCTAACT 1140 TGTTTCACCA CAGATGCATT CCTGGTGGTC TTCACCTGGT GGGTATTAAG AGTTTCTTTA 1200 TCTATATACC AACCATATTT ATCCAGGGTG ACTGTAAGGA TTAAATTAAA TGCTATAATG 1260 TAAAATGCCA AGCATCTGCC TGGTACTAGA AAGTACACAA CAAATATTAG TTCTCTCTCC 1320 TCTACGAGCT CAAAGTAAAG TTATGTGTAA TTTTTTTATC ACCTAAGCAG TTCTTCACTA 1380 TCAAGAAACT GCATCTCTGC AAAACATAAC TAACAGCCAG AAAATTAGCC CTCCTAAAAA 1440 GAGAATTCTA AGCAACCAAA ACAGATATGA TCAAGTCCAT GAAACAAAAG ATACTCACTT 1500 TACTGTGAGG TAACTCCTAA 1520
|