| Tag | Content |
|---|
EnhancerAtlas ID | HS101-11485 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr12:119645960-119647050 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr12:119646468-119646489 | TCCTCTGTCCATGGTGCCCGA | - | 6.14 | | ZNF263 | MA0528.1 | chr12:119646082-119646103 | GCTCCCTTCCCTTCCTTCCCC | - | 6.04 | | ZNF263 | MA0528.1 | chr12:119646083-119646104 | CTCCCTTCCCTTCCTTCCCCC | - | 6.25 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_27404 | chr12:119644947-119647266 | Esophagus | | SE_49178 | chr12:119646051-119647288 | Right_Atrium | | SE_51246 | chr12:119645554-119647647 | Skeletal_Muscle | | SE_54793 | chr12:119644070-119647327 | Stomach_Smooth_Muscle |
|
| | 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 |
| GH12I119207 | chr12 | 119645696 | 119647284 |
|
Enhancer Sequence | CACACCCAAG TCCCTTCCAG ATCAGCTCTC TGAGGCTTCA GGTGGCTCCT AGACATCACC 60
ACTCACAGGA TTCTCAAACT GCACATCTCC AAAGGAGAAT CCACTATCTC TCCCTGCAAA 120
CTGCTCCCTT CCCTTCCTTC CCCCAAGTTA GTACTCAGCA CAAACACCTT CCCTGCAGAA 180
ACCCCAGAGC TCTTCTAGAC TTCTCTCCTT GTCAGCTGTC ACCAAGCTGC TGTCCATACT 240
CTCTGATCTG TATCTGCCAA TACTGTCCTC TGCCATATGA GTTCTGTTGT CCAGCAATTG 300
TCACTTTACA AAATCCAGTC ATCCATTTAT TACTTAACCC TTACAACAAG TCGAGGAGGT 360
GGATGGATGG TATCATCTCA ATTTAAGGAA ACGGAGGATC AGAAAAGGAA AGCCATCTGC 420
TTAGGGTCAC ACAGGAATTA GAAAGTAGAG CTGGGGTTTG AACCTAGAGA TGACTGAGCC 480
TAAAACCCAT GCTGGTCCCT CCAGGACCTC CTCTGTCCAT GGTGCCCGAA TGCAGGAGGA 540
GCAAGATCTA AGCCCGTCTC TCTCTGGCAG GTTACTAAGG TCCACAGTGC AAACAGCAAC 600
AGTGTTGTTC ATGAGCTCAT CTGCTCCATC TTGCTCCACC CAGCCCTAAT CCGGGCTCAT 660
GACCTGGGAA TTCATCTCCC AGGCAACCAG AGTGATGCAA CAAACAGAGG AGCTGCCCAG 720
GCAGGATTGG TGCAAGCCCA GGACCGTGGC TGACGTTCAA GGGCTCCAGC CCAGAATGCC 780
CCCTCTGTGG AATTAGCACC ATGTGCCCCT GATGAGCCAG AGGAATCCAA AACCCAGTCC 840
TGGCAAGGAC AACAGAGGCT GGAAACATGG GGAGGCTCGT GACCTGCAGT CATCACAAAA 900
CACTCATTGT GCATCCTGGG GTACAGGGGA GGGTTCAAGA GACCCACGTT TTGTGTCTTG 960
CCCCAAGAAT TACTAACTCT GCATACAATT CATCAGGAAA TCCTTCGCTG CCAAATGTAT 1020
CCAGTGTCCA AACACTTCTC ACCACCTCCC CTGCCTCCAC CTTGATCCAA GCCTATGTTA 1080
CAGCAAAGGT 1090
|
