| Tag | Content |
|---|
EnhancerAtlas ID | HS053-27573 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr3:105316640-105318170 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr3:105317639-105317654 | AAATGAGTCAGCAAT | + | 6.49 | | Nfe2l2 | MA0150.2 | chr3:105317637-105317652 | GAAAATGAGTCAGCA | + | 6.1 |
|
| | 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 |
| GH03I105597 | chr3 | 105316452 | 105319007 |
|
Enhancer Sequence | TTTATATAAA GGATAGCATA TTCTTAATAC TATTCTGCCC CTTGTCTTTT TTCAACTAAT 60
AGCATATCCC AGCAATCACT TCATATAAGT ATGTAGAGAT CAGCCTCCTT CATTTTTACA 120
GCTGCATGGT ACCCCGTTCT GCGATCATGT TACAGCCCAG TGGGTTCTTC TTGCTCACTT 180
TCCAGAAAAG CCAATGCAAT GACACTAGCA AGAGTGTTGC AGCAGAGAAA AGTGTTCATT 240
TATTGCAGGG CTAGCCAAGC AGAAGGGTGG AAAATGTTTC TGAAACCTGC CTCTCTAAGA 300
ATTCAGAGGC TAGGGTTTTT CAAGGATAGT TTGGCAGGCA AAGAGCTAGG GAACGAGGAC 360
TACTGTGATT GGTTGGGCTA GGGAATAAAA TCACAGGGGG TCAACATTGT CTTCTTCTCT 420
GAGTCAGTTC CTGGGTGGGG AAAACAGGAC TGGTTGAGTC AGTTTCTTGG TATGTGTTAC 480
TTGTCAGGGT GTACCAGCTG GTCCATCAGA ATGCAAGGTC TGAAAAATAC CTCAAACATG 540
AGTCCTAGAT TTTACCATAA TGATATTATC TATAGGAACA ACTGGGGAGG TTACAAATCT 600
TGGGACCTCC AGCTACATGA CTGCTTAACT GTAATTCTAA CCTTGTAGCC AATTTGTTAG 660
TTTCACAAAC GTGGTGTTTG TCCCCAAGCA AGGCAAGGGT TATTTTCAGA AGGGACTATT 720
ATCATATTTT AAGGTTAAAA TATAAACTAA ATTCTTCTAA TAGTTAGCTT GGCCTATGCC 780
CAGGAATGAG TAAAGACAGC TTTTGAGATT AGAAGCAAGA TGGAGTCAGC TACGTCAGAT 840
TTCTCACATT GTCATAATTT TTGCAAAGGT AGTTTCAATT ACACCATGAC TGAGTTAATC 900
AGTTCCCTAT TGGTTGTTTT GGTTGTTTCT TAAAAAAGAA AATAACTTTT ATCTGAGAAA 960
TGCAGGTCCT TTTAAATTAT CAGGCCCAGA GAGACATGAA AATGAGTCAG CAATCATGTC 1020
CTATTACCTT ATTGAACCAT GTATCCATCT CTTGAAACAG CTTGCTATTG CCACAACTTA 1080
ATAATGCCAT ACCAGAGACT ATACCACACA CCCTATAACC TAATAATATA TGTAGTCAAT 1140
CACTAAGCGA TGTTATTTCT CTAAACCAAT AAGAATTCCT AACAAACAAC TTTGTATCAA 1200
CCCATTTTCT CTCTCTTTGT TTTTAACTTT TAAAAGCTTG GTTGTAACGA AGGAGAAATA 1260
AAGTTCATAT CCAAGATTAT CGGCTCTGAG TTTTCTGGGC AGCTGTCTTT GCTTTGGCTT 1320
AAGTAAACTC TTTGAATTAT ATTTTGTGCC TCAGCCTTTT TCTTTTAGGT CAATGTGGGG 1380
CCCATAGGCT CTGGCTCTCC TAAAGGTTTG CTGAGAAATC ATTGAAGCAA GGCAGATTGA 1440
TTAACAGGAA AAAAGCCATA CATATTTATT TAATGTTCAT ACATGGGAGG CTTTATTCTG 1500
AAGACCCAAC TTCCCAATGA GGCACAGAAG 1530
|
