| Tag | Content |
|---|
EnhancerAtlas ID | HS108-08141 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr11:74817660-74819110 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr11:74818513-74818534 | TCTCCTCCCCATTCCTCCTTT | - | 6.59 |
| | | 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 |
| GH11I075106 | chr11 | 74817821 | 74818665 |
| Enhancer Sequence | TAAGTGGGAG CTAAACATTG AGTACACATG GACACAAAGA AGGAAACAAC AGACACCAGA 60
GCCCACTTGA GGGTGAAGGG TGGGAGGAAA GTGAGGATCA CAAAACTACC TATCAGGGCC 120
AAGCACAGTC ACTCATGCCC ATAATCCCAG CACTTTGGGA AGCCGAGGTG GACGGGATCA 180
CTTGAGGCCA GGAGTTCAAT ACCAGGCTTG GCAATATGGC GAAACCTTGT CTCTACCAAA 240
AATACAAAAA TTAGCCGGGT GTACGTAGTA GCACATACCT GTAATCCCAG CTACTCAGGA 300
GGTTGAGGCA GAAGAATCAC TTGAACCCGG GAGGTGGAGG TTGCAGTGAG CCAAGATTGT 360
ACAACTGCAC TCCAGTCTGG TAACAGAACG AGACTCTGTC TCCAAAAAAA AAAAAAAAAA 420
AAAAAAGACA GTCCTGGGTT GCTCATTGCT CTATGATTGA TTGTGAAGCC TAGCTCCCAG 480
ATTTTGAAGT GGTGACTGGA AAATGCTTTG TCTAAAATGA ACATGGGACA AATGACCCTC 540
CTGTGTGAGA GCTCCCTAAT AAAGAATCTC AGAGGTCACC CCCATGAGCA GTACAGGAGT 600
TGAACATGGA CTATCATCAT TCTAAAGGGT TAATGCTCAG TTAACTAGAG CCCCATCCCA 660
GCAGATCCAA TAGAAAGGTT TTCAATGCAC CCAAAACGAT GCAAACTGCA CTTCCCTGGA 720
CATTGCTGCA GTCAGAGTGT GAGTCATGGG CTGACTGTCT CCACGTTAGG CTGAGTTGGG 780
GGGTTTGAGT GACAGAAACT AAGAAGGTCA TAGCCAGAGG AGCCGTAAGA GGCCATCCAG 840
TCCAGCTGCC CTTTCTCCTC CCCATTCCTC CTTTCACTGC TTTGCTGACA CCCCAGCGAA 900
GAGGTGGTCC AAGGCTTTTC ACTGCCAGGA CTATCCAAGG GTCATATCAG GCTTGAGTCA 960
CCAGCAAAGC AGGGTCACCA AAAATACTTC CTGAGAGAAT GTAACATTTG ATATTTCAAA 1020
ACATCATTCA AATAGTCCAT CATAGGAAAT ATCAGAATTT GGCTGGACTG TCTCAACACT 1080
TATTTTATAG GTTAGGGTTC TTATTTTATT TTGAATTATA TACTACATCT AAGTAATACA 1140
GCCCTGTGCT TAGGGCCAAA AGACATTTTC CCAGGGCACA GAACTTGCCC AAGCAGATCT 1200
TTCCTGTTGG GTTTTTACAG TGCTGGTGGG GAAGAGGGGT CAGAAAAACC AACCACCTGA 1260
ATGTCCATCC TGCACTTTCT GTACGTCATC TCTCCCCATC AGACAGCTCT GCCAGGAAGT 1320
GCTTATGCCC CTTCAACTAA TGAAGAAAAC TGAGGTCAGA GAAGGCCAGG CCCTCCTTCA 1380
AGGTCACAGT TGGTGAGTGA GAGCAGAGGC TACTCCTGGA GCCTGGCAAC CCACAGTCCT 1440
GCCTCCTGGG 1450
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