| Tag | Content |
|---|
EnhancerAtlas ID | HS007-03456 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr11:121799440-121801550 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr11:121800011-121800032 | GGGGAAGGGGAGGGGAGGAGG | + | 6.07 | | ZNF263 | MA0528.1 | chr11:121800591-121800612 | GAAGGAGGGGAAGGCGGGGTG | + | 6.19 | | ZNF263 | MA0528.1 | chr11:121800010-121800031 | GGGGGAAGGGGAGGGGAGGAG | + | 6.52 | | ZNF263 | MA0528.1 | chr11:121799746-121799767 | GGGGGATGGGGAGGATGAGAA | + | 6.84 | | ZNF263 | MA0528.1 | chr11:121799738-121799759 | GGAGGAGAGGGGGATGGGGAG | + | 6.92 |
|
| | 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 |
| GH11I121928 | chr11 | 121799358 | 121801624 |
|
Enhancer Sequence | TCCTTCTACA TCCGTCCGGG AACTTCGACT GCTACTATGC TACATCAGGT ATGCAATGAA 60
AGACAAACAA CGAGGACTCC AAACAGAAGA GGGGAGCTTC AGTAACTGTA GTTTTTATGT 120
TAGGGAGAGA CTGAGAGAGA AAGGAGCATT GTATCTCGGA TTAACAGAAC TGCAGGATTT 180
CATTAATGAC AGCCCAGCTT TTTAGCAAAA GGAAGATAGT TAGGGCAGTA AAAGAGAACA 240
TGACTAGAAT GTGCTCTGCT AATTGGAAAT GTATATTATC TTCAGACGAT GTGAGTGTGG 300
AGGAGAGGGG GATGGGGAGG ATGAGAAGAG ACACATACTG AGAGGCCTGC AGGAGAAAAC 360
TGGACCCAGG ACGCCCCAGA TTTGGCCACA CCAGCAGGGC AGTTAAAGGG TCCTTTCTTG 420
CTGGTAGGAA CGTCTAGTGC CAGGACCCCA CCCTCCCCCA CTCCCTTTTA ATTCAATGGC 480
TACGTAGGGG CTTCTTTGAT GGAGGCTTTG AAGTCGGTGG CTTTGAGATT ACTCTTCCTC 540
TGTGACCTTG ACCACCAGCC ATGAGGTTAG GGGGGAAGGG GAGGGGAGGA GGAAGGCGCT 600
GGAGTTGGAA AAAGGAAAGG AAAGAGAGGG GAGGGGAAGG AAGGCCGCCC TAAGACATTT 660
CTGCAGCATT CCACGACTTT TCTGATCACT CTGCAAAGTT GAAATATGAT TGCAGCCTTT 720
GCACCGGGAA GGAAAGAAAC CATTTAAATG AAAAATTAGC TGCCTTAGCA GGTCAAGCAC 780
ATAGTTACAT TAATGTCGTG TAGAACAATA AATCAACTTC GATCTCCAAT TGAAAAAATG 840
CTAATTTAGC TCAGCGATTC ACTGATTGTA CTTTCCTCTG ATAGAAATCT TTTCTTTTAT 900
TTAATGCGAA GCCGTGATTT GACAGCCTCC TCTAATGGTG CTTGCAGACT CTCAGCATTT 960
CAGTGGAATT CTGATCATGG TTTTAATATT CCGTGCAGCT CTGCCCCCTC TGATTTCACG 1020
CTCACACATT AACGAGAGCT GACACTGGAG ATTAGACGCA GACAGCTGGA ATGCCAGGTC 1080
TTTGTTGCAG CATGGACAGG AGCCAACGTC GTTCAACCAC AGCCAAGAGG GACCTGGGAA 1140
AGTCTTCTTA AGAAGGAGGG GAAGGCGGGG TGGGGGGCTT GAGGGAGGGT GGGAGCGGGG 1200
GATGGGAGCA AAAAGAAAGG CAAGGTAGTT TCTGAAGGGC ATATGAAAAT AGATGTTTTC 1260
AGAAAGCCCT TTCGTCTCTG AAATTCACAT TGGAATCAAT TCTGGTTTAT TTAGAGGAAG 1320
TGGTTCATTA CAGGGAAATC CCAAATTGGT TGCAGTATTT TTCTGTAAAC TCTGAAAATA 1380
CAAGTGTGAT GCACGAAAAT GGAAATGGCT CCTGCTTCAG CTGCTCACTA GTTCGTCTGA 1440
GAAACAATGG TGATTACGAG CTGGAGGAAG AGTGCTTACA TAAGGAAATG TGTTCTCCCC 1500
TTTGCCTTAA AAAAAATCAC TTAGTTCCAG GTGAATAGAT GGGGAAATAA AACGAGATTT 1560
ATGAGCCAGG GCTGCCTGTG CGACTAGCGA CTACCTCGGC AAGAAAGGAA GTCGCGTAGC 1620
CTAACTGCCT TGATCCTCAT AAATTGTTTC CTGATACCAG AAATCAAATA AAGATCCATA 1680
GTTTCATCTA AACCATAAAG CCACTTGGGC TCAGCTAGTG CCGATATTGC AAAGGGGAAG 1740
GAAGGGTGCT GCCTGAGACA CTGGCTCAAC TTTGTCCGAA AGAAGATGAC AGATGACCAA 1800
AGTTGCGGAG GCGGCGCATT AATACTATGT CAAAAAAAAT TGTTTCTGCT CCTGGGGGAA 1860
ACCAATTGAG TAGAAATAAC AAATGTCCTT CTTGCTAACT GTATCATTAA TAATAATCGT 1920
ACTTTGCATT TTTATGGGAT ACCAGGATTC TAGAGCGCTT TATAAATATT CATAGGGGAA 1980
GGCTGGGGAA GGGAGGTGAA TGTACCCATT CCTGATGCCT GGCTGGAGTG ACTAAGACTC 2040
AGGGCCCTGC AGGGGCTTAA CTGGAGTGAA ACAGCAAATC ACAAAGCCCC ATGCTGCAGC 2100
TGGCTTGGAG 2110
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