| Tag | Content |
|---|
EnhancerAtlas ID | HS112-00353 | Organism | Homo sapiens | Tissue/cell | KELLY | Coordinate | chr1:46927260-46928700 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EN2 | MA0642.1 | chr1:46927954-46927964 | CCCAATTAGC | + | 6.02 | | TCF3 | MA0522.2 | chr1:46927290-46927300 | AACACCTGCT | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTCCTCTGGT GTTAACAATC GGAAGCCAAC AACACCTGCT GGTCAGAGAT AGGGGAGCCT 60
CAGAGACCCT TTAGCCCAAG GGATGGGTCA CAAACAAGGA CTCAGTGGAG GGGAATTTGA 120
GAGAGCAGGC TGTGGCCTTG GACCCGGGCA CTGCATGATG CTCCAGTGGA TATGAAGGGG 180
TCTATTCCAG CCCAGCCCAG GAAATCATTC TAAAAGGGAC CCTATCTCTT TGCAAACCAA 240
ATAACCTTCT CTCTGGGTGT GGGCAGAGGC CCTGGCAGCC CCCCAGTGCC TATCACTGGT 300
AGACCTATCT CCTCCCTCCC TTTGGAGACC AGACCCTTCA CCTTGCAGTC TGTAGGGTTT 360
GGGCTGGGGT TGCCAGTCCC TGCCTCCCTC CTGGTCTCCT CCCTACTGCC TGCCAGAACT 420
CTGCCCCAAC TAGGCTTGGC CTCAGAATAT ACCTGGACCA GCCCCTCCCT TTCACTGTCC 480
CTGCCCCACA GAAGTCCAAG GGCTCCTCAG CTCTCCATGC ACAGCACCCC CCACCTCTGG 540
AGTGGGCTGA AAAACTCTGC TGTCCTGCTC ATCATCCAGA AGGCCCTTCT TGTTCTGCAT 600
TTCCTCCCAC CGTTGTGTCC CACGGGGAGT CATTTATCTG ATCGACTGGC TCTCCTCAGT 660
GCAAACATTC ACAGGAGCAT TAACAAGCCT AAAACCCAAT TAGCCTTCAA TTACTCAGGC 720
CTTAGTCAGA TTTTCTGTGG TGGGGACAGG GTTGAGGAAT GTATTTGGAC ACTGCCTGGG 780
TGGTACTCCT GCCCTTTGGC CAACGCCCCC ACCCATGCAC TAGCACTCCT GTTGCAGCCA 840
GCCTGCTCTC CTCTGCGCTC CCTCCTGCCC TATACCACCT TCTTTCCTTC TTATTCTTCT 900
CTCCTGACCC CTTTCCTACA CCTCTCTAAA AACAATCATT GTTTTAAAAT GTACATACCC 960
AATACATGGG TTTGCAAAAA CTCATAAAAA CATAATGCAA AAGAAAAGAA AATGAAAAGC 1020
TAAATCCCGC TCTACCTCCC ATCCTGTAAA TCCTGCTGTC AGTAATTGGG GGTTCTCATT 1080
CCTTCCCTGT GTTGGATTCT ATACATTTAC AACCCCCCTC AACATAGTTT TAAGTGTTCT 1140
TTAAACATCT TCAAATTGGG ATCACACTAT ATATGAATAG TCATATAACT ATTCATACCT 1200
ACTCTTTTTT CTTTCTTTCT TTTCTTTTCT TTTCTTTTTT TTTTTTTTTT TGAGACAGAG 1260
TCTTGCTCCA TCACCCAGGC TGGAGGTGCA GTGGTGCGAT CTTGGCTCAC TGCAGCCTTT 1320
GCCTCCGGAG TTCAAGCGAT TCTCCTGCCT CAGCCTCCCC AGTAGCTGGA ATCCTAGGCA 1380
TGCCCACCAT GCCTGGCTAA TTTTTGTATT TTTTCGTAGA GACGGGGTTT CACCATGTTG 1440
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