| Tag | Content |
|---|
EnhancerAtlas ID | HS089-10389 | Organism | Homo sapiens | Tissue/cell | Hela | Coordinate | chr5:134926660-134928090 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr5:134927528-134927549 | TCTCTCTCTCCTTGCTCCCTC | - | 6.22 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTCAACCCTC CTGACTCTAA GGCTCATGTG CCACCACAGC ATCATCCTGC CTCTCAGTGC 60
TGCCTGGCAC TCAGGTAGGA GCCTCCAGGG TATCTGGGTG ACCAGAGCTG CCTTCTCTCC 120
AAAGCTTTCC CCTAACTGCA GGGTGCCTGT GATTCCACTA TTAAGCTGCA CTTCTCTGGG 180
GTCCCTACAC CCCCATGATG ATGCAAATGC AAAGCATCGG AGGTCACACA ATGACCCTGC 240
AGATATTCTC ATGCCACTCT GGGAGGCAGG CATTCTGATC CCCTTTTAGG GTATAAAGAA 300
ACTGAGACCC AGAGCAGAGA AGGGACTTAC TCAGGGCACA GAAGTGTGGC GCATTTGTTC 360
TCAATTGTTT GCCTGATGTC TAGAATAGTG CCTGGTGCAT CACTTGGATG TTCGGGGGAT 420
GGTCCTTCTG TGCCATGGAA CATGACTCAG GACCTGGAGG CAGGAGCACG GGCCTACACC 480
ACCCATCATA GCTGCCTTCT GGGCCCACCT CCAATTTCAG TGGCAGCTGT GTTGGACAGT 540
TCTGACTCAC CTCTCCCTGC CTCAACCCAC CTGGAGTGTT CCATGTATCC TGCTTTCTTC 600
TGCAGCGCTT GCTCCAGCCT ACGCAGCTCC CATTGCTTTT CCTCAAACAG CCTGGAGATG 660
TGGAAGGGGC TTTGGGTGGC CAGAGTGCAT ACCTCTGGGG CAGATCCCAG CCAATGGGGA 720
GTGGGAGCTG GTGAGTGACT GTTCTGGCCC TGCCTTTCAA GGAGCGGTTC TGGGAGGCAA 780
TTGAATGCTT TCAGAGACCC TGGCAAAATG GGGGCCCTAT TGCCTATACC TGTGACGTTG 840
ACACCCACCT TACCTTTTCT CCTTTTAGTC TCTCTCTCCT TGCTCCCTCC CTCCTGCTTC 900
CTGGGATTTC TCCCAAATAG ATCACTCAGG CTCTGTGAGC GGAGAACCTA AGCTAAGCAG 960
CTTCTTGGCT GAACCTGCCC CCAACTCTTC AGAGGCAGTG AGGAACTCCT GGGATGGGAG 1020
ACTTTGTAGT ATGAAAGGCC TTTGAGAACC ACAAAGCTCT GTGGTTCTCA AAGAGAACCA 1080
GCTCTGCTTG TGTTAGAGTG GGAAACAGGC CAAGTTAGAG GACTGACTGG CCCAAGGTCC 1140
CTTAGTGCCA AGGCAGGACT AGAGCTTGGC ATCCTATCTC TGAGGCAAGG ATCTACGGTG 1200
AGAAGAGGCT CCATGCCTGT CTCCTGGATT TGGTGAAGTG GTGGCAGGAG GAGAAACATG 1260
AGCTGATGTG CCACACACCT ACTAAGCGCT GAGCCCTTCA CCCCCGTGGC CTCATCAGGG 1320
AGGCGTGATG AAGCCTGGCC TATCAGGAAC AGGTGTTTTC TGCTGCTCCA GGAGTGCTCT 1380
TCCATTCCTA AACATCTTGA CTTTGTTCTG TCTCTGAAAG TTCATTATGA 1430
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