| Tag | Content |
|---|
EnhancerAtlas ID | HS048-07311 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr11:77279060-77280760 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr11:77279563-77279584 | CTTCCCCCTCTTCCCTCCCCT | - | 6.04 |
| | | 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 |
| GH11I077568 | chr11 | 77279168 | 77280639 |
| Enhancer Sequence | AGGGGAAACC CCAAGTCCAG TAATGTTGTG GCTCTTGCAG ACTCAGAAGT AGTGCCTTAG 60
TGGTCTTGGG TAAGATTTAG GAGAATTCCC TGGATTACCA GGTAGAGACT CTTGTTCTCA 120
TCCTTTACTT TCCCCCACAA ATGAAGTCTC TCTCTCTCTG TACTGAACTT CCTGGAGCTG 180
GGAGAGGGGT GACATAAGTT CCCCTGTGGT CACCACCACT GGGACTGTCC TGGGTCAGAC 240
CTGAAACAAA CATAGCACTG GGTTTCACCC AAGGTCCACA GTGACCGTTG CTTGACTACC 300
ACTTAGGTTC ACTCAAGACC CAAGAGATCT ACAATCAGCA GGTGGCAAAT ACAGCAGGCT 360
TGTGTCCTTC CTTTTAGGGT GGTAAGGTCC CCCTGGCCCT GGGTGTGTCC AAAGATGCCA 420
CTGGGAGCCA GAGTCTGGAG CCAGGAACCT TAGAAATCTT ATCTACTGCT GCTGAGCTGG 480
CATCCAAGCC ACAAAACAAA GTCCTTCCCC CTCTTCCCTC CCCTTTCCAC AAACAGGAGT 540
CTCTCTTCAT GGCTACTGCT GCCCTGAGCC CGTGGCAAGT ACTGCCAGGC TACCACCAAT 600
GTTCACTCAA CGTCCAAGGG CTCTTCAATC AGCTTGCGGT GAATGCTGTG AGGCCCGGGA 660
CTCACCCTTC AGGGAAAAGG ACTCCCCTCT GGCCCAGGGC AGGTCCAGAA ATGCCATCCA 720
TGAGCCAAGA CCTGGAACTG GGGACACCAA GAGCCTGCTT GGTGCTCTAT CCCACTGTGG 780
CTGAGCTGGT ACCCAAGCTA TAAGACAAAA TGCCCTTTAC TCCTCCGTCT TCTTTCTTCA 840
AGTAGCCACC ACAGCTAGGA ATGTGCTGGG TCACATCTAA AGGCAACACA GCTCTGAGTT 900
TTACCCAAGG CCCAGGAGGA ATAATGCCTG GTTACCACCG CTGATTATTC CTTCCCTTTA 960
AGGCAGTTGG TTCCCTTCTG GCCCAGGGTG TGTCTTGAAA TGTCATGTGA TGGCTAGACC 1020
CTGGAATGGG GTCCTCAGGA CTCTGTCTGG TGCCCTATCC TGCTGTGGCT GAGCAGGTAT 1080
CCAAGCTGCA AGACAAAGTC CTCTTTACTC TCCCTTCTCT CCTCAGGTAG AGGGAAGGAG 1140
TCTCTCCCAG AGCTGTGAAC TGCACTGCCT GAGGTTGGGA GAGGGATGAT GCAAGCACTG 1200
CCTTGGCCTC CCTGGCTCCA TGTACATGTT ACATGTACCT GAGTACGAGT ACCCTGGCTC 1260
CAAGCCCAGC ACAGCACCAG GACTTGCCCA GCAATTGCAA TCCTTAGGGC CTAGACTGCC 1320
TTTCAAGTTT ACTTAGGACC CCAGAGCCCT TTACCAAATG GTGGTGGCTT GCCAGAGGTC 1380
AAGTTCTGAC CACTGGGATG GGTAATATGC CTCTGGCTAG GGCTGATGCA AATGCTCCCT 1440
CCTTGGCCTC CAGCTGAGTT CTGCCTTGTG TTGTTTTCTG CTGTGACAGG GCAGCACTGA 1500
GCTCTAATGC AAAGTCCCAT AATCACTGCA CTCTCCCTCC CACAAGTGCA CAGACTCTCT 1560
GTGCTATGCA GCCACAGCTA GGCGATCAGA GAAGGGTGCT GTAGACAATT TGAGACTATT 1620
TTTCCTGCCC TCTTCAGTGC CTCTTTCCTT AATGTGATGT TAAAACCAGG TACTATGATT 1680
ACTCACCTGA TTTTTGGTTG 1700
|
| |
|
|
|
