| Tag | Content |
|---|
EnhancerAtlas ID | HS101-41923 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr7:156336980-156338450 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RARA(var.2) | MA0730.1 | chr7:156337670-156337687 | AGGTCAGCTAGGGGTCA | + | 7.16 |
|
| | 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 |
| GH07I156544 | chr7 | 156337165 | 156338237 |
|
Enhancer Sequence | TCCTAGCAGA GGCTGTCTGA TTAGTTCACT CTGGGCTAAA AAGGCAAACC ATTAAAGGCA 60
TTAAAATTTC AACAAGAACG TTATCTCCAC AGTCAGCACA ATAGTGACAT CTTGTGCCTA 120
GGAACTCGGG AGATAGCACA GCCCTGCCAC TTCTCGGGTC AAACCTGGGG CCCCAGGAAC 180
CAGCACACGG CCAACCGCGC ACAAAGACTA AACTATTTAA AACGTTGACG GTTCCTCCAT 240
AGACGGACGG ACTCCAGCAA GGGAGGCTGC TTTTTGAGTT AGACTTTCCA TGTGCAGAAC 300
ACAACTGGGT GGTCCTAGCG CCTTTTCTCA TCATACAAGA GAGTCTGCAG CTTCCAGGCG 360
TTCCAGGGCC AGGGTTCCAG CCCCACTCAG GCCAACTTTA AATCACGAGC CCATTCTTCT 420
TCTGTAAAGT AAAGGCCTCA AGTCTGAGGT CAAACTTTTC ATATTTACAG TTCTTGGATT 480
ATTTTCATTA GGAAGACTAT TAAAAGGAAA TAGAAAGCCT GTCGCATTGT CAGTTAACAC 540
ATTTTGTATC ACATTAAGAC AAAGACAGTG CCTCTCTGTC TCAAGGCGTC CTCGGTTAAC 600
ACTAACAGTT ACCTGTAGGC ACAGACCCAG GCAACCACAG AACTCCAGCA CAGCACACAG 660
AAGGCGCTTC CGTGGCTCCC ACACACCTGA AGGTCAGCTA GGGGTCAGCC GATCTAGGCT 720
GGGTTCAGCT AGAGCAGCTC ACCTCTGCTC CTCCAGTCTC TTCCTGGGAA GAGTGGGCTA 780
TCCTGGGCCA GGTCCCAACT CAAAGGAAGT GGGCTATCCT GGGCAAGTCC CCAACACAAA 840
GGAAGAAGTG CAAGAGGCTG GGGGAAAAAA GGCCTCTGAG TTCTAGGCTT ATGCCCCGTT 900
CCATACGTCA ATGCAACTCA CACATCTGAA TCCAAAGTCC AGGGCAGGAA AATGCAAAGC 960
ACCCCTTCAG CAGGTGGAGC TGCAGAGTCA CATGTGTGAA GTCATGTGAA TAACCCGAAG 1020
TCTAAGGAGG AGTAAAGGAG GGAACAGGAA GGCAATCTAC CACTCCACAC TGGGAGAAAA 1080
GTGAACGGAA ATGCAGAGAC CCCATCTGCA TTTCCATTGT TCCTTGCACA GTAAACGCTC 1140
CAACCAACCC AACTACCAGA ACCCACTTAT TTGATTTAAT TTAATAAGTA TTTGTTTTGA 1200
CTCTGTCTGA CCAAGCCTTG GTGGTAGGCC AGAATCGGGG AACTGGTTTA CCCACCTCCT 1260
ACTCAGGCCT CTGGACATGC ACCGCCTGGC CAGAGATCAC ACCAGGTAAT ACGGGGGCAT 1320
ATGCATTCAA TACTAATGAG GCTTCCTGCT CATTACACAG AACACCAGAA AACACACACA 1380
AGATAAGTAC AGGTTTCATT CAATCACTCT TTGAAAACAC ATCATCAAAT TCAAATGAGT 1440
AAAGCAAACA GGTGTGTATT CCGAAGTAAA 1470
|
