| Tag | Content |
|---|
EnhancerAtlas ID | HS180-32484 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr3:10261480-10262870 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr3:10262103-10262124 | CTTTCCTCTTTTCTCTCCCCC | - | 6.22 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_35045 | chr3:10261326-10262990 | HeLa | | SE_58615 | chr3:10208482-10269048 | Ly1 | | SE_62498 | chr3:10211834-10316085 | Tonsil |
|
| | 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 |
| GH03I010220 | chr3 | 10261707 | 10262951 |
|
Enhancer Sequence | AGGTGGGCTG GACCCTGCTG GGGCCTGGGC TGCAAGGGTG GAACTGGTGC CTATTCCTGG 60
CTCACCTCCC GCTCCGCCAC TCACCCCTGT CCTCTTTGTT TTTCTCTTCC TACCTCCTCT 120
CCTCTGCCCT CCCCTGGATG TCTTTTTCTC TGTTATGCCC TCAAAAATGA GTGTTTCCGG 180
GCTGTGCTCC AAGTCCAATT GCTCTCAGGA TGAATTGCCT ACCTGTCACA TTTGTCTTTC 240
TGAGCTGCTG TTTTCCCAAC AAGCCCTCCA CACCTTGCTG CGTCGCACTG TCCACTCAGC 300
AGCTGGCCTG GACCTCATCC TCGAACTTTG GGCCATGTCT GCCAACCCCC TGGGATTTTG 360
AGCTCCTCGT TCAGTGTCTT TTCTGAGACC TGTCCCCTTC TTGTGTAGCT GTTGGTGTTA 420
GCATCTTGTC TGGAAGGCTC CTGCAGGTTA GGCCTGCACC CCTGCATGTC AGTGCCATGC 480
ACATGAGAGG GAGAGGTCCC CATCTGGAGA CGGTTAGGAT AGGGAGGGAT TCCGAAGATA 540
CCAGAATATC TGGCAGAACT GGCTCCAGAG ACACAGAACT CGTATTTCCC CAAAGTTCTC 600
TTTCCATTTG ACTTGTGGAA GTCCTTTCCT CTTTTCTCTC CCCCAATTTT TTTTTTGTTT 660
TTTGAGACGG AGTTTCACGC TTGTCACCCA GGCTGAAATG CAGTGGTGCG ATCTCAGCTC 720
ACTGCAACCT CCACCTCCCT GGTTCAAGCG ATTCTCCTGC CTTAGCCTCC TGAGTAGCTG 780
GGATTACAGG TGCTCGCCAC CACACCCAGC TAATTTTTGT ATTTTTAGTA GATAGGCTTT 840
CACCATGTTG GCCAGGCTAG TGTCGAACTC CTGACCTCAG GTGATCCACC CGCCTTGGTC 900
TCCTATAGTG CTGGGATTAC AGGTGAGAGC CACCACCCCG GCTCTCTCCC CTAATTTTTA 960
TTTGATTGCA TCAATAATTC TAATAGCAGG CAAGGAAATG AAAGGGTGAG AGAGGTCACC 1020
ACTAACCTAC CCCATGACTC ATCAGCTGGC CTCTAGGTTT TGTTTCTTTT TTCACTTCCT 1080
GCCTATACAA ATCCTTAGTC CTGAGGTAGC ACCTGGGTAC CAATTCACAT CCTGTTTTTT 1140
ACCCCTTCAT TTAAACATAG TAAACATTTC GCTACATTGT ATACCGTCAT GTTTTTTAGT 1200
GTCTTAGTCT TCCCGTGAAG GAATTTGCCC ATAATTTACT TAACCACTCC TGGCACACAC 1260
ACCCGTGCAT TTGCGGGCGT GCACACACAC ACACGCTAAA AAAGTTTTTT TTTTGGCCGG 1320
GCGCGGTGGC TCACGCCTGT AATCCCAGCA CTTTGGGTGG CCAAGGCGGG CAGATCACGA 1380
GGTCAAGAGA 1390
|
