| Tag | Content |
|---|
EnhancerAtlas ID | HS147-38138 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr7:42035930-42037440 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Sox6 | MA0515.1 | chr7:42036591-42036601 | AAAACAATGG | - | 6.02 |
|
| | 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 |
| GH07I041995 | chr7 | 42035327 | 42037430 |
|
Enhancer Sequence | AGAGCCACGG CCAATCCACT TTCCCAGTGG TCTTCACTGA GCATCAGCAG TTCAAACATA 60
CCCAACCTGT ACCTTTCAAA TGCTCAACAC AGAGAATTCC CCAAGGGTTA GTCAACCGCT 120
GGCTCATATA CAAAGAAAAT ACTGTATTTT GCTCTGAAGA GCTTTCTGAA TCAATTTAAA 180
CACAGTGAGA CAGACACAAT ATCCCAGAGA GAGGAAAACC TACCTTATTA CATTCCTGAC 240
CCAAGAGAAA GGATTTGCCC TTAGGACATA AAAGGAATCT GAGGGGGTAT GGGGAAAGAA 300
TTATCTAATC CTAAACGTAA AAACAGTTCA TAATGCAGCA TGACAATGCT TTTAATCGCT 360
GACATAATTG TAATATGTAT ATATAATATG ATACAAGGAA GGTAAATGCA GCTTGCTTTT 420
CAGCCTTAAA GGCTCTCTTC AATATTCTAC TTAAGGTCTT CTGGATTTTA TGCATGCTTG 480
GGGGAATTTT CAGGGGGAGG TAACGTGATA TTATAAGGAT TCTTTCTCAG TAAGATCACA 540
TCTTGTTCTG ATTTGATTTG ATGCATCTGT ATGTGGCAAG TGTGGTAAAG TGAAACTAAG 600
CTCTGTGAAT GCAGTGTTTT ACAATTCCTC CTTGATTTCC TGTGCAAGCC CATGTGGCCA 660
TAAAACAATG GGCAGAAGAA TTGGGATTTT TATTTCTTCA TATGGGAAAG CTGCTGGGAG 720
AGACACTCCC GTAATCTCAG CTGTGAGTGG TGTGGGCGTT CACTGTTTTC CTTTCAGGGC 780
TATATAAAAT ATATTTTTTA ATGGGAGTTG AGTTTTTCCC CCAGATGTTT CCATACATGA 840
TATAATGTAA GCCTATGGTA CCATCTCCCA GGAAGGAAAG GCATCCCTGA GTGATTGGTT 900
GGAAGGCTGA TAAAGAAACC TGACATTTTG AGAAGTCCAG CTTTTTTTTT TCTTCTTTAA 960
CATTATTTAT GGAAAGAATT TTACAACACC CTTAAAAGTC ACTATGTGGT GGCTGGACTT 1020
TACCAACTTT GCAGGCTGAC ATTTTTACAC TAGGCATGGC TGGGACCTAG GAGTTTTGCA 1080
GTGTTCACAT TTTACTAAAG TGAACGCTAC TGACAATTCT GGCAGATGCC AATGATCATT 1140
CCAGAATACT GAGTATCAGA TCCACTATTG CTCTTTGCGG TCATATGATT AGATGAGCAA 1200
AAGAAAAAAG TGTCCAAGTA ATAGAAATTT AAAAATAAAG AGAGAAAGAG CTGGTGTTCT 1260
GGCTGGACGT TGTGTGTGTC CTAATTCTCC TGAACATCAA AATCCCTCAA ATGATACCTT 1320
CTGCTTTGCT TTCTAGCTGG GTTTATTTTG CGTGAGCATG GCTTTGACCC CTTCTGGACT 1380
GCTTCCTGAG TAGAGGAACT GTATCACATT CATCCTGGTA CCCCACAGGC CTTCACCCTG 1440
ACTTCCACAC GCAGGTGCTC AGGAACTGGT GCTTGGTGCA ACATAAATAT ATAACTTGAA 1500
CCAATAATCT 1510
|
