| Tag | Content |
|---|
EnhancerAtlas ID | HS187-22085 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr6:157040530-157042000 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr6:157041200-157041211 | GGGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr6:157041201-157041211 | GGGGCGGGGC | - | 6.02 | | NR2C2 | MA0504.1 | chr6:157040942-157040957 | AAAGGTGAGAGGTCA | + | 6.51 | | ZIC3 | MA0697.1 | chr6:157041364-157041379 | GGCCTCCCGCTGCGC | + | 6.4 |
|
| | 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 |
| GH06I156717 | chr6 | 157039132 | 157043763 |
|
Enhancer Sequence | TTACAGGTGC CCGCCACCAG GCCTGGCTAA TTTTTTGTAT TTTTAGTAGA GACTAAAAAT 60
TCGCCATGTT GTTTCGCCAT GTTGGCCAGG CTGGCCTCGA ACCCCTGTCC TGAGGTGATT 120
CACCCACCTC GGCCTCCCAA AGTGCTAGGA TTACAAGCAT GAACCACCGC GCCCTGCCAT 180
TAACGTCTCT TAAAGCACAC ACTCTGTCTC AAAGGCTGGA GGGTTTGGGA ACGTTCTCGT 240
CCTTTCTGTG ACCCATCTAC CACAGTCTTG GGGGTAAAAG CCCCGGTTTA AAAAGCTGGG 300
AAATTCCACC TCATGGCCAC GCGGTCTCAG CAGCTCTGGC GACTGGGAAA CGTAGGGTTA 360
CAGGGCGGTA AAGATCATCA GAAAGGAGGG CTGAGGAGAG AAACTAAAGA CTAAAGGTGA 420
GAGGTCACAA ACCCTGAAAT TAGTAAAGAT CTACGTTGTC GGGGGTGGGG GTGCGTGTGC 480
GCCCAGCAAA AAGCCTCTGC GTCCACACAG GGATCCACCG CGGGGCTTCT GGAACTCACA 540
GGCTCCCTCG GAGCCTTCAA AGACGCGACC TGATTGACAA CAATTTTGTT TACACACCAC 600
ACGCCCTGGG AAAGCCACAC ACCAGTGCCG GCGTTCCAGA CGCTTCCTCT GCGCAGAGCC 660
GGCCCAGGAC GGGGGCGGGG CGGGCCCTGT TGCTCAACTC ACCTCTCCCG CCCCGCACCC 720
GCTCCCCGGG GAGGCGCCGA CCCAGCGAAA CTGGTGCATG TGTCAGCCGC CCAGCACCGG 780
CCCAGGAGGC CGGCCGCGCC GCAGGCCGGC CTGGGAAAAC GCCCAGCGGC TGCAGGCCTC 840
CCGCTGCGCG CTGCGTGGTT CTGCACTGCA CTCAGGACCT GTCAGGAGCA ACACACACGC 900
ACATGCACAC GCCCACACAC ATGCACACAG ACACACACGT GCACACACTG CGTCGGTAGG 960
AATAGCTCAG AGGTGCCCTT CCTTTCCAGG CAAAGTGCTT AGTAGCTGAA TTCAGCGAGA 1020
AGAAATCATC CAAAGGTAAC CCTTGCTCTG AGCCCTCCCC AGGAAGAAGA GAGAGGTCAC 1080
TCTGGAAAAG CCTGGAACCT TCTCTCGCTT GAGGGTGCGG ACAGCAGCCC ACCTCCCCTT 1140
TGGCTAGGCC AAAGATCTCT CCTTCCTTTT AGGCCTAGCT TTCCCTGTCA CTAAAAGGGC 1200
TACATTTATC CTTAAATATC ATCTAAGCTG AAATACTACT ACATTGCTTT GCAGTCGGTC 1260
ATAGTGGAAT CTTAGTTTCA GAACTACATT CAACACCTAC TGCGCAGAAG CACCACATGG 1320
ACACTGCCAC AAAAATTAAC ACAGTGGATC CTAACAGAGC TGAATGGGGT TGCTGTGAAT 1380
ATCTCCCTAG TAAGATAGGA AAAAGGCCCA TGTGGGCTAT GATATTTGTA TAAAGTGGTG 1440
TCGATGAGCT CATTGCAGGA CTAGCTATTT 1470
|
