| Tag | Content |
|---|
EnhancerAtlas ID | HS113-19995 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr2:106157260-106159070 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TEAD1 | MA0090.2 | chr2:106158310-106158320 | CACATTCCAT | + | 6.02 | | Tcf12 | MA0521.1 | chr2:106158203-106158214 | CAGCAGCTGTT | - | 6.32 |
|
| | 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 |
| GH02I105541 | chr2 | 106157647 | 106159025 |
|
Enhancer Sequence | AGTGTCATCA CAGGAAATGA GCTTAAAAGG AAATGAGCCA GCTCGGAGCT TGGCCTAATC 60
ACTAGGAAAT GGCCCTCATC TTTTCTGTAG GTTATCAATC CCCTAGCTCA TCAGTGGCCC 120
CTAAGAAATG CTGTGCCTTG TGGCATAATT ATGCTTAATC ATGTAGACTG TTGAGTAAAC 180
TTATGCTTAT GCCTTTCCTG TTCCATGTTA GGTGTTATCC ATTCAATTCC ACTTCTTTGC 240
AATGGTGAAG CCCCGTTTTG ATGATACCTT CTTTTTGTAA ATAGCCTTTT TTGCAGATTA 300
ATGCAGGGTC TACTGCACCT TGGCCCAAGT GGCCTCAGTT AATATTTGAT GAATGAGTAA 360
ATGAATGAAT GAATTAATAA ACCCATCTGG ATTTCAGGAC CCTGATATCA GCAGGAGACG 420
AGTAGAAGGA GGAGCCTTTG AAGTCAGCAG TGTCAGCTGG CTGGCAGGGG CCAGGTCATT 480
GCCCTGGCTT GCTTCGTAGA GACTGTTCCA GTGACAAGTT CCTCATAGCG GGGTGAAAAC 540
GGAGGTGGGG AGAAGTCATT TCTTAACTCA CCCCTGGGAA GCCCAGGGCA AATAGCAGGT 600
GCCTTCCCCC ATGACCCTCT CTGTCTCCGA GGCCCACTCC CATGGCCTTC CTTGTCTCTT 660
GCAGGTGCAT CTCTGCCTTC AGTATCAGGG ATCAGGGGAG ACTGTTGTCA GGGTGTGGTG 720
GGTGTCACCA AAATCCTCAT CCTCCTGTGT GGCAGCCCCG CCTAGAACGA GGTTGCAGTC 780
AGGGAATCTG CCTGCCCCAC GTTGGAAAAA GCAGGCACAG AGGATTCTTT GGAAGTGAAA 840
ATGCCCATAG AAAATTTCAC AAGGTCTCGG AGGATGTGCT TGAAGTCCAG GGTGCGGTGT 900
GCCTGTGGCT GATGTTTTAG GGGAGGAGAG TTCTCTATGG ATGCAGCAGC TGTTATTGCT 960
GGGTGGATTT GCTTCACACC CTTTGTTGAT TCACAGCCTC AACATGCACA CAGGTGAGCA 1020
GTAGCAACTG CCCTCTCCTC CGCCCTTTGT CACATTCCAT CCAACACCAG TTGCTGTCTC 1080
TCTCATTCCA AGCTGTCTCC TAGGCCTGCT AAGCAATATA CTAGCAATTA GTGGTGACTG 1140
AGTCACACCT AAGTATTTCA GCTTCTTTCC TGTATTCTAT AGTGGCGTTC CCTCCTCTTC 1200
GTCTCCTGTC CCTCCTGCAC AAGGCACTCT GTAGCAAACA TTAATCTGAT CCCATTAAAC 1260
AATGCAATGC CCTCTACATT GCCTGGGGAC AGGTCTGAAG AGATGCTTGC AGCCTGCCTT 1320
GAGTGCAGCC TGGCCTCGAT CTCCTCAGCC ATGCTCTGAC CACCATGGCC ATTTGGCCTT 1380
CCTGTCACCA TCCCAGGCTT CCACTTGCGT CCTAGGCTAG TTGGGTTTAG TCCGCATCTA 1440
CCTCCTCTCT CCTTTTGCTG ATTTCTCGGA AGCGCGGCTG ACAAATTGCT CCTTTCCAAA 1500
GCAATCCTGT CTTCTGTATG TTTTTTCTAA AGCCCTTCTT ACCAACCACT GTCCCAGCAC 1560
CATATGATGA CTTAGTGACA TGCCTTTTTA CCTCACCCTC CACTGACCAG GAGCCAAATG 1620
TATAACACAA TTCCTGACCT GTGCTTGGAG GGTGGTGGAA CAGGCCACCC CAAAATAGGT 1680
CACTTTGGCA GAAGGATTCT CTTGAGCTGA AGGCACTTGA GAAATAGCAG ATACAGGAAG 1740
GGCATTCGAA TCACCCCTTT TCTTCCTAAA AACAAGGGAT AAAAATCTCC CACGTGAAAA 1800
ATGTACTCTC 1810
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