Tag | Content |
---|
EnhancerAtlas ID | HS101-36803 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr6:13733170-13734330 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr6:13733228-13733243 | TGACCTTTTGACCAG | - | 6.56 | RARA | MA0729.1 | chr6:13733225-13733243 | CCTTGACCTTTTGACCAG | - | 6.76 |
|
| 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 |
GH06I013732 | chr6 | 13732961 | 13734611 |
|
Enhancer Sequence | AAACAAACGT TAAATAGCTT GACCCAAATC ACTAAAAAGC CTCAGATCTG GAAAACCTTG 60 ACCTTTTGAC CAGTATCTCT TTCTGAAGTC ATTGGGGATA TTATCATTTT GGTTTTTTTT 120 TTGTCTTGTT GGTGTTCACA ATGAATAAGA AGACAGTGGC TTTGGCTTGC ACATTGTATT 180 CAGGTGATGG TATCAAGCCT TCTCTAATCA CCCCAATCTA ATATCCAGCT AGTCAAAACA 240 GACCTAGAGC ATAACATCAC ACGATCACAA CACACAGTAC ATCCATTTGG CAGCTGCTGG 300 GAGGACAGCC GCAGTTCCTC TCGGCTGAAC GTGGCTCCTT TAAGGGGCGG CCGCAGGAAA 360 GAATGCATGT GTGCTGCCAA AACAACATGT GAGCCGGCGA AGATGATCCT GAACTTGAGC 420 ACGTGAAGAG GGTGATGCAA AACATAGACC GCGCTCTTTC TTTTTGGCAA AAACAAGAGA 480 CAAAAGACAC CTTGCAGGAG AGAGGAAGGG AATTTTTAGA TGTGATAGTT ATAGCCATGT 540 TCAGAGGATT TTCCCATCAA GTAGAATAGT TGAGTCTAGT TCCATAAGTA ACTGGATACA 600 CATGTACACA CACACACACA CACACACACA CACACATATG CACGCTCGTT TAGTTGCCCA 660 GGGAGTATCT TAAGAAATCA AACTAGCATT TTGACTTTTG TTCCATATGT CAGGGATCAC 720 TCAGAGGTTG CCTCTGAGCA TTCTTGTTCC TTGTGGAGCA CTGAGGGGAA TGACTGCTTT 780 AGGATAGGGC TTTTTTTTTT TTTTTTTTTT TTTTAGGATA GGGCTAGCTC ATAAAGAACT 840 GTTTGCTGAA GTCCTTTGTT TGCTTAACTA CCATCCTGAA TCAACGTACT CTTGTGATGC 900 GGATGAGACT GTTAAAACGA GGCTGGACAA GAGTGCGCAG TGTAAATCTA CTCTCAAACA 960 CACAAGCGGT TGAAAATGCC CCTATCTGAG AAACTAAGTA ACAAATGAGA AGCTTTTGTG 1020 CTCAAGAGAG GTTCTGTGAT GATTCCTTTG TTTAGCAAAT ACCTCAGTTA TTTTGGCTAT 1080 GTATCTGCAT TTTCAATTTT CCGGGTGCTT AGTTTAAGTT CCACCTGTAC TAATCAGAAT 1140 GTTGTTTTAA AAAAAATACT 1160
|