Tag | Content |
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EnhancerAtlas ID | HS088-10316 |
Organism | Homo sapiens |
Tissue/cell | HeLa-S3 |
Coordinate | chr11:66153280-66154690 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr11:66153811-66153830 | TGTCCACAAGGGGGCAGTC | + | 7.02 | Foxd3 | MA0041.1 | chr11:66153455-66153467 | AAACAAACAAAC | - | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 66153824 | 66154400 | chr11 | 66154294 | 66154411 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I066386 | chr11 | 66153543 | 66154271 |
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Enhancer Sequence | GCAAGAGCCA CCATGCCTGG CTAATTTTTG TATTTTTAGT AGAGATGGGG TTTCACCATG 60 TTGGCCAGGC TGGTCACCAA CTCCTGACCT CAGGTGATCC ACCTGCCTTG GCCTCCCAAA 120 GTGCTGGGAT TACAGTCGTG AGCCACCGCT CCTGGCCAAG ACCATGTTTC TTAAAAAACA 180 AACAAACAAC AACAACAAAA CAAATATCTA TATCTATATC TATATATCTA TATATATAGA 240 TATAGATATA TATACACACA CACACATAAG CAGAGGGACA GGAACCAAGA ACATCACACG 300 ATTTCACATC CTAGGGTCCT CCAGAGCTCA GATTATAGAT GGATGGCCGG GAGGGGGTGT 360 CTACCACTCT AATTTGTTAA TCACCAGAGA ATCGCTTGAA CCCGGGAGAC GGAGGTTGCA 420 CTGAGCTAAG ATTGCGCCAT TACACTCCAG CTTGGGCAAC AGAGCGAGAC TACATCTCAA 480 AGAAAAACAA AAACAGCTTG GCTAAAAAGA CCAGCTCGGC CTTGCCAGGA GTGTCCACAA 540 GGGGGCAGTC GAACATTTGC TTACGAGTTC CCCAAGGGCG AAAGATCGGT TTTTAACCTC 600 ATTCAGGAAC GGAAGATGGA ATCTCGGGCT TTGACGGTCG ATAAATTAGA AATAAGATCC 660 TTGCACAAAG CCAGAACCCT TGAAGGGCTG CAATCACTTT GTAAGGAAGA CCAGTAAACT 720 TCCCACTGGC CAGGGAGGCA ACCGGGAAGC TCATCTCAGC TGTTGCCTTG GCTGGGAATA 780 AAACAAGGTT TCCTAATCTC CAGGCGGGCA AGGAGCCTAA ATCAGTCTAT TCCGTGGGAA 840 ATTCAAGCTG ATACATTATC ATAAAAATTA ATCCCAGGCT GTTTCTATAT CATGGTCTGA 900 GTTTTTGTCC TCCTATTCCA ATAAATGTGT TGAAACATAA TCATCAATGT GATACTATGG 960 AGGGGGGTGA TTAGATCATG AAGGTAGATT CCTTATAAAT GGAATGGCGT CTGTATAAAA 1020 GAGGCTTCAG GGAGTTCCCT CACGCCTTCC ATCATGTGAG AACACGTGAG AATGTGCAAT 1080 CTGTGAACCA GGAAACAGGT CTTCACCAGA TAAAGAACCT GAGAGTGACT TGATCTTAGA 1140 CTTCCCAGCC TCCAGAACTT TGGGAAATAA ATTTCTGTTG TTTACAAGCC ACTCAGTCTA 1200 TGGTATTTTG TTGCAGCAGC TCTAACAGAC TAAAACAGCA GAAGCAACTA CAAGAACACT 1260 TTGGTGGAAC ACAGCCCTTC TCAACATGCT CACAGCCATA TGAAGAAACA ACTTCCCATG 1320 AGCAAGAATG AGCAGACAGC CATCAAAAGC ATTACCTCCT TTAGGGGCTA ACTCATGTTT 1380 CTGGGTAGAA GCTTTATAAT AAGTCTCAAC 1410
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