| Tag | Content |
|---|
EnhancerAtlas ID | HS187-21732 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr6:130341160-130342610 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MNX1 | MA0707.1 | chr6:130341573-130341583 | TTTAATTACC | - | 6.02 | | RREB1 | MA0073.1 | chr6:130341169-130341189 | TTGTGGGGGGAGGGTGGGGG | - | 6.14 | | ZBTB18 | MA0698.1 | chr6:130342477-130342490 | CAGCCAGATGTTG | + | 6.25 | | ZNF263 | MA0528.1 | chr6:130341866-130341887 | TCCTTTTCCTCCCCCTCCCCG | - | 6.21 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GCGGCGGGCT TGTGGGGGGA GGGTGGGGGC GGCGCGGGGC TGCTTTTCCT GCAACTTGTT 60
TACGCCTGCC TTATTCTGGG GAGGAAAAGA GGGGTCGGGG CCGGGGCCGG CGCCGGGGCC 120
ACCGCCCGCC TCGCGCCGCG TGTGTGTGCG GTTCCGGAAT AATGGGCTTT GCACACTCGC 180
GTCCTGGGCC CCGCGGGCCG TCCTCGCGCC GCGGCGGCGG GGCGGGGGGA AGTAGAGGCC 240
GGCGGGGGTG GGGATCGGGA AGCGCAGGAG CCGAGGCATC CGCCGCGCGC CCCGCGAGCT 300
GGTGGAGTGT GGGGGCCGCC GGGCGGGGAG AAAAACTTGA GAGCCCTGGA AGGGGAGGAG 360
GGCACGGTGG CACGGGCGGG GGGAGGGCGC AACTTTTGGA CTGGTGGTAA AACTTTAATT 420
ACCTTTAAAG AAAAAAAGGC CCTGCGATTC CCCCCTCCCC CAGTCCCGGT CAAAGCACAG 480
CCCGCAGCGC GACCGTGAGA GAAAGTTTAA AAGCGGGCGT GTTCCTCCCG GGTCCCCGCG 540
GAGGGCTGGG GGCGTCGGTC TGTCCGTCGC GCTCAGAGGG AGGTGGGGGT AACTAGCCGC 600
TTTCCAGGGC GCGGGGACCG CGGCTCTACC CCACCCTTCC ACGGGAGACG GAGGTAAACG 660
TTGCTTCGGT TTCCCTTCTG AGTCCCCCTG CTGCCACCAC CCCGCTTCCT TTTCCTCCCC 720
CTCCCCGCCG ATTTTTTGAG GGGACCCGAA AAACGGAGTC CCTTTCCTTA GGCAACTTCC 780
TCGGGCGCTG TGAGCACGGC CCTCCCCCTC ACCGCCCCCA CCCCCAACGC CTCGCATCCC 840
TTGGCCCGCT TCTCCACCTC GGGGCCACCG CCAGAAAAAT GCATTCGAGA TCATTCAGAG 900
TGCACAGAAA CAAAAATAGA TTTTTAATTG TTAGGTTAGG GGAAACTGAG ATGAGAAATA 960
AGAATTTGGG GTGGGGGGGC GCGGCCGGGG CGAGTGCGTC CAGTTCTCCT TTTGGTTTTC 1020
CTAGAGCGTT GTTTGTGATG TCTTTATTGG TTTAGGGAGT CCGAGAGGCT CTATGCTGGC 1080
TATCTCGGTC GCGTGGATTT TTGCGCAAGT TTTTAGAAAA ACACTGACTC GAGTAGAGAG 1140
CATTTCTCCG GAAAGTTTCA AGTGCAGCAA AATAGCGAAC GTGCAAAACT GGCCAAGGGG 1200
AGACCTCTAG TGGTTGAACG CGTCTTTTAA GTTCGGAAGG CCGAGAGCAA AGTTTGGCCT 1260
TTACTCGTAG CTACGTAGTC CGTTCAGACG TGGAAGTAAT TAGAGGACCT GAGCGAGCAG 1320
CCAGATGTTG TGTGAAAGGA TGCTGATCAG AAATTGAAAG TTTAGTAAAT CGAAGCAATG 1380
AATTCTGAGG ACTCAGACCC TGTAACTTCC ATCCGACATG AGTTATATGG GAAAGACACT 1440
TTGCTTTTAT 1450
|
