| Tag | Content |
|---|
EnhancerAtlas ID | HS101-10773 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr12:67667790-67670190 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXF2 | MA0030.1 | chr12:67669696-67669710 | GAAACGTAAACATT | + | 6.34 | | IRF1 | MA0050.2 | chr12:67668170-67668191 | AGATAGAAAGTGAAAATGTAA | - | 6.14 | | Nr2f6(var.2) | MA0728.1 | chr12:67669090-67669105 | GAGGTCAGGAGTTCA | + | 6.22 | | Nr2f6(var.2) | MA0728.1 | chr12:67667833-67667848 | TGAACTCTTGACCAC | - | 6.22 |
|
| | 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 |
| GH12I067274 | chr12 | 67668181 | 67668380 |
|
Enhancer Sequence | ATAGTAGGTC TGGGACTTAT AGGATCTCTT TACCCCCAGA ACATGAACTC TTGACCACCC 60
AGCTATGTCA CTTCTCCAGG GTTTAGACTA GTGGATGTTA AGATTCAGGC CTTAAATTTC 120
ATTTCCCTCT AAAATTAGGC TTATAGAATA TTTCATGCTA GAAGATGCTT TTAATAATTC 180
CTGAGGACTA CAAAAAGTTT AAGATCTGGT GCTTACTTTC CCTAAATCTA CATGCTTGTT 240
GAATAGTTAA GACACTATTG TAAAAAGATG AATAACCCAG GGCAATATGT AATTGTCAGG 300
CATTAAGTGG CAGAGAATAT TAAAGCAAGA AGATTCATGT CCATGGAGAG ATTTGAGCCA 360
GGTGTTGAAA ATGAAACTCT AGATAGAAAG TGAAAATGTA AAGCACACGA TACAAAACTT 420
CACTGGGGAA GAGGGAATAG ATAACCTGAC TGTAGCTGGA TGGATATTGT CCACAGAACT 480
CCTTAAGAAT AGGGACCTTG TCTTACTAAA CGGAATCGTT CTCTTTGTCT GGCTCTGGGC 540
CATGTGGGTT CTCAGTAGGT GCTTGTTTAA GTAGAATTGG GTTTTATTTC CATTATATAG 600
GGATTTTAGG AACCTCCAGA AAACCATTGT AAAATCAACT AAACTGTTTG TTTAAATACC 660
ACTTGATAGA ATCTTCTTAA AATAATTCAC CCCATTTTGG AATGCAAGTT TTTCCCAATT 720
TGATAAAGGT TTATATTACC AGATTTATTT ATTTAAGTGT TTTGGATATT GGACGGTATT 780
TTCTTTTGGA AACTGTTTAA AATGCTTGTA AAAAAAACTC AAGCCTTTTA AGGAATCAGG 840
TTTTCAGAGC TGGAAGGAAC CTTAGAGATC CTATCATATA GCTGAAAGTA CAGTGTGGGT 900
GGGCATTTAC AATAACATAA CAGGAAATAG TGAAATTATC TTAAGTACTT GTGCTTGGAG 960
AAAAGCAGGT TTAATCAGAA GAAATAGATT TGCAGAGATT AAGAAGGTGA TTTCTGGGCA 1020
CTTTTAAAAA TACTTAGAAG GTTGATGGCA GTAACTTTCT TGATTTTACT TTGATGTTTT 1080
TTTCTTGATA TATACTATGC TAACTGGTTA TCAGCAGTGA TTAGGGCTCA CCACTGAGAA 1140
AGAGGAGGAA GGGACCTCAC AGAGAAAACT GGGAAGAAAG ATTAGTAAAA ATTAGATTTC 1200
TTTACATGAA CAATATTAAG ACTATTCCAA TTTAGGTCTT GTGTGGTGGC TCACGACTGT 1260
AATTCCAGCA CTTTGGGAGG CCAAGGCAGG CAGATCATCT GAGGTCAGGA GTTCATGACC 1320
AGCCTGGACA ACATGGTGAA ACCCCATCTC TACTAAAAAT ACAAAAATTA GCCGGGCATG 1380
GTGGTGCATA CCTGTAATCC CAGCTACTCG CGAGGCTGAG GCAGCAGAAT TGCTTGAACC 1440
TGCGAGGCAG AGGTTGCGTG AGCAGAGATT GCACCACTGC ACTGTGGCCT GGGTGACAGA 1500
GGGAGACTGT CTCAAAAAGA AAAAAAAAAA AACTGTTCCA ACTTAATTCA TAGCACTCTA 1560
AGGAATAACT GAGGAAAAGT GAAATAGCAG TGGTGTATGT GCAGGATCTC TGAAAGGTAA 1620
TTGGTGTACT GAGTGATAAA ATTGACCATA TCAACTAGAT TTCTGGTTGG AAGCAAGAGT 1680
AAAATTGTGT TTATGTATGA TGGGAGAGGC TGTGGTGAGA GTTATTGTGA GTGCAAGGTA 1740
TCTATCGATC TAGTGCATAC CTAGTGTAAG TTCCAGACTG TGTTACTCAT CACTGTGTTT 1800
GCAGAGTAGA GTTCCTTATG TTGGTGCCCT CAAAATACTT GTTGAATAAA GGAATGAGAT 1860
GGCACTGCCT ACAGGTCATA TCAACCTGGG AATTCCATTG AAGTCTGAAA CGTAAACATT 1920
TATCTTTTTC TTTTCCCGTC TTAATGCCTT CTTTATCCTT ATTTTGGCCT GTTAAATTAC 1980
CATCCACTGA AAGTCACAAG CAGAAAATCT TTGATATCAC CCTTCTCCCG TCTGTCTTCT 2040
TTAGTCTCCT GATGAGTATT TCTCAAATTA ATCTTGCTGT CTCAGGCCTC TTCCTAACCC 2100
AGTTTGTTCC CTCTGGCCAT TAGAATTTTC TTCCTATATA CTGCAGCTGA TCATTGCCTC 2160
CCTCACTAAT TTCCATTGAC TACAAGATAA ACTCCAGATT TCTTAGCTGT TGCCCATCTG 2220
AATTCGTAGA GACTGCTCTC CTAAAATCCC CAACAGTCTC CCTAGTCTCC TAATATAACT 2280
CATTTAGTGG ATATTTTCTT TGCTCATCTA TTTGGTATAT TTTTTTAAAT CACTTTTTCC 2340
TTCTTGGAAT TCTCTTATAT GGGCATCCTG ACACGAGTTG GGTTTTTGTC CGTAATAGTC 2400
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