| Tag | Content |
|---|
EnhancerAtlas ID | HS007-04249 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr12:122205150-122206620 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr12:122206416-122206437 | GAAAAAAAAGAGAAAGCACGT | - | 6.18 | | Zfx | MA0146.2 | chr12:122205309-122205323 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | 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 |
| GH12I121765 | chr12 | 122203081 | 122206677 |
|
Enhancer Sequence | CCGCGTCCCG GGTTCACGCC ATTCTCCTGC CTCAACCTCC CGAGTAGCTG GGACTACAGG 60
CACCCGCCAC CACGCCCGGC TAATTTTTGT ATTTTTTAGT AGAGACGGGG TTTCACTATG 120
TTAGCCAGGA TGGTCTCGAT CTCCTGACCT GGTGATCTGC CCGCCTCGGC CTCCCAAAGT 180
GCTGGGATTA CAGGCGTGAG CCACCGCGCC CAGCTGCCCC TGCAAGCTTT AACTTCTGTG 240
GTGAAATGAG CCCAGAGAGT GACTGCAAAT GGGTGTAGGT TTCTTTCTGC AATGATAAAA 300
AGGTTTTAAA ACAGATTCTG GTGACAGTTG CACAACTCTG TGAATATACT AAAAGCCACT 360
CAGTTGTGCA CTTTCAGTGA GTGAATTGTA CGGTATCTGA ATCACATCAC AGTAAAATGG 420
CTACATAAAC ACATGTGCAC ACAACCAGCC CAGAGCCCCG GGGTGTGCAG ATGGACGCCT 480
GGGCTTGTGA ATGCCGGGCC AGGGAAGGAG CGATTTCTAG CCTCACCCGA TGTCACTGAG 540
CTGTGTTTAT TGGTGGCATC TGTCAGAGCT GGGCTCTGGG CACGGCGAGC TGTGAAATGA 600
AAAGCTGCTG CTCAGTCAGG CTTGTTGCCT GGAGTCTGTG TCTGCCTCAG GCTGCTCCTA 660
GACAGAGGGC ATTTCTCAGG GGAGCTTTGG GAGCAGGACA AAGGAGTGTG GCGCCTGCCA 720
AGTGCTGAGG GCTGACGTGG CTCTGCAGAG CTCTGGGAAG TTGCAGAGAG ACCTCCTGGT 780
TGCTCTTCAA GCTGGAAGTT GGGGGATCTG GCCAACTGCC TTTGCTGTCA GAAATTTGGA 840
GCCCAGGGGC TTCTTAGACT CTGACAGGCG AGACTAGGAT ACATGAGTGG AGGTGGGAGT 900
TTTCTGGGGA CAAAGAAGTA GATGGACATC TCACCCTGTC CCCATGACCG CACGTGGCAC 960
CTGCAACAAT CTCCTGTCAC CTCTGCGCTG GTGGCATCCA GATTAGCTGC TGCTTTCACC 1020
AGCCACACCT CCCAGGCATC ATTCATGTCA ACATTTATTG AGTGCCTGTT GTTTACCTGG 1080
TGCTGTTAGT GCTGTGAACA CAGAGCTGCA TAAAACCTTG CCCCTCAGCA TAACTCCTGG 1140
GGAACACACA GGCTGTTGCT TGAAAAGCCA ATTTATGCCC AGAACTGTTG CATGGGCCGT 1200
CAAGGGAAGA GTGATGGTTT AGATCCAGTC TCGTTCTTAC GATGTGCGTA TGCGAGACCC 1260
TGCCTGGAAA AAAAAGAGAA AGCACGTGGG CGTGTGTGTG GACCCATTTC CCTGCCCAGT 1320
CCCAAGAGAG TTCTGGAGGG ATGAAGGTTA ATGACTGTTC CCACGAGCAT CCCCAGCCTC 1380
CACCTCCCAG TCCTGGGGAG GAGGGAGTTG GCTGCTCCTG GGTGCATTTG GCAAGTTGCT 1440
GCCATGTGTT TGGACTAGAG GAGCCTGGGG 1470
|
