| Tag | Content |
|---|
EnhancerAtlas ID | HS091-13612 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr14:73414680-73415810 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr14:73415396-73415415 | GCTCGCCCTCTGGTGGCCA | - | 6.71 |
| | | 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 |
| GH14I072948 | chr14 | 73415341 | 73415490 |
| Enhancer Sequence | ATTCTCTTAT TAAATGTGTT CTGGAAACAA TGTGACTACT CATTGTACCT CACACCTACT 60
TCCTGAGTTG TGGTGAGATT AACATTAGTT AACTCCTGTG AAGGCACCTA GCAGTTTCTG 120
GACATCATTG GTCCTCGACA AATGATAACT GAATCAGGAT CTTTTTTGTA AATTTTATTT 180
GTTTCACAGC ACTGTATTTC AAAGGAGTTT TTTTGGATTT TAATTTTTTT CAGAGAAAGG 240
GGTCTTGCCC TGTCACCCAG GCTGGAGTGC AGTGGTACAA TCATAGCTCA CTCCAGCCTA 300
GAACTCCTGG GCTCAAGTGA TCCTCCTGCC TTAGCCTCCC AAGTCACTGG GACTGTAGGT 360
ATGCACCACC ACACCCAGCT TACATTTCAA AGGGTCATAG AGCCTAAATA CATTAGCGAC 420
CTGATTATAA ATTTATATAA GGCATCAAAC TATGTGTGTT CTCTAAATTG CAAATTTTAT 480
GTGGCTTTCA TTTGATGGGG TTCTGTAGGC CAATGGGACT GACCACATGT TACTATGATG 540
ATCTAACCAG AGGGCTAAAG AGGCCAAGCT CTGCAGAAAG CAAAAACAAG AACCTCACTC 600
ACATTTCCAG TCTTAAAACA GCATGGTATT CTCGTTTCTG TGGGCTAAGG AGAGGAAAAA 660
AAAATCCATG TAATTGGACT TAAAGGGATG GATGGTCTGT TGTAGCTTCA TCAGTGGCTC 720
GCCCTCTGGT GGCCATTTCT GGTAGCCTTC GGGCTTTTGT GCTGAAGATT TTTTGTGCTG 780
CTTCAGAAGT TCAGGTAACT TTTTCCCTTT AGAAAAATGG TACTTTGTTC AGACCTGCAC 840
TCTGCATTTT TCCTGCAAGA GTGGTGGGAA GTTAGATGGA ATTCTTTCTA CACTTATTGG 900
GCCCTTAGTT AACCTGTGGC CTGTCAAAGG ATTAAATCTT AGCCTGGCTC CGTAAGTACT 960
CAAAGTTTGA GTATAAATAA GCTGAGATTC AGCAACAGTA ACTAACATGC ACATCCCACT 1020
TTCTTCACTT CCTTGCCTTC CAAACCCAGA AGCAAAATAA GTTTATTTGG TGGTGGTGTT 1080
CTCATTTACA GTTTCAGCAC CTGGTATATC CTGGAGATAC TTAATTTGGA 1130
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