Tag | Content |
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EnhancerAtlas ID | HS095-04940 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr11:10436120-10437550 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr11:10436161-10436179 | GGAAAGAGGGGAGTAAGG | + | 6.05 | EWSR1-FLI1 | MA0149.1 | chr11:10436153-10436171 | GGAAGAGAGGAAAGAGGG | + | 6.07 | Foxd3 | MA0041.1 | chr11:10437141-10437153 | GTTTGTTTGTTT | + | 6.32 | NFYB | MA0502.1 | chr11:10437066-10437081 | CTGATTGGCTCCATT | - | 6.06 | Zfx | MA0146.2 | chr11:10436756-10436770 | CCCGCCTCGGCCTC | + | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr11 | 10436257 | 10436513 | chr11 | 10436121 | 10436688 | chr11 | 10436794 | 10437029 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I010413 | chr11 | 10434867 | 10437360 |
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Enhancer Sequence | ATGAACAAAG AAGAGAGCTA AAACTTAACA TCTGGAAGAG AGGAAAGAGG GGAGTAAGGT 60 GCCTGAAAAT AATTTCCTTT AGGAGTGACT GGAGGCTTCA GGGGGATCAC AGCACTCCTG 120 TGGAATTTTT ACAGAACTAA GGAAGGCTGG AGTCAGCCAA ACTTTTGAAA CCTCAGCATC 180 CTAAACCTCA ACTCTTGCTG CCCTGAGAAG AGCATGAGCC GGCCAAGCCC TGGTGGCGGC 240 TTCCCCAGGA CCTCCCACTT CCTTCCTGAT GTGCCTGCAG TCCTGGAGCT GTGATCGCCT 300 CTTCTTTAGC TTCTTAGAAA AGAGGCGGCA CAAGAAAAAC GCTCAGTCAT CTTGCAGAGA 360 CTTGGCATCT CTCAGCAACA CGTTCTCTCT TTCTCTCTTT TCTTTTTTCC TTTGAGATGG 420 GGTCTCGTTC TGCCGCCAGG CTGGAGTGCA GTGGTGTGAT CTCGGCTCAC GGCAACCTCT 480 GCCTCCTGGG TTCAAGCGAT TCTCCTGCCT CAGCCTCCGG AGTAGCTGGG ACTACAGGCG 540 CACACCACCA TGCCTAGCTA AGTTTTGTAT TTTTGGTAGA GACGGGGTTT CACCATGTTG 600 GCCAGGATGG CCTCGATCTC TTGACCTTGT AATCCACCCG CCTCGGCCTC CCAAAGTGTT 660 GGGATTACAG GCGTGAGCCA CCACGCCCGG CCGACACATT CTTATTAACT TGATGGCACA 720 GTTGGCTGGC AGGTTCCCAG GTCATGTTCT CAGTGATTGG AGTTCTTGCT GTTTCTTGGA 780 CTCCTTCATG TCTCACCCAG TCCTAAGTCC CTTCCTTGCT TCTTAATTAA TTTATGTCCT 840 TGTGTAATAT GTGGCACACC CACATAGCCA TGAGGCATGT TCAGGCTGTG TTTTTTAATG 900 TTCTGGCTTG TTCTACATTT GCCAAGTGGG CAAGGACAGC AGTTACCTGA TTGGCTCCAT 960 TTGGGCAGCA GAACCTAAAC AGTGACTACC TGTTGGAATC CACCTGGCCT AGGTATCTTT 1020 TGTTTGTTTG TTTAAATAAC AACAAGCATT TCTTATGGTG TTTTGTTTTC TCCTGAACTC 1080 TGTAAAGACA ATGGCAACAC AGAGGTCAGT CTAGAATGAC TATACTGGCA CTAGGAGATG 1140 AGAACTATAC AAGTGGAATT AAGCAAATGT ATAGACACAA AATCATCACA AAAAGGGTGA 1200 AGTGCTGTTC AGTTATTGAT GCCAGTCCCT CTTCTCTAGG GGACTGTGAC AGCTGTAGCC 1260 AGATGTGTCC AGGAGATTAT CTCTGTCCTG ATTCTGTCAG CATCCTCTTC ATTTATTGTC 1320 TGGTTTTGCT TCTAAGTCTT CTTCTGCATC TCAAGCTGTC TGCATGCCAT ACTGTCTGCA 1380 TTGAAATGAT TTGCTTGCTT AAAATGAGTC TTGGCCAGGT GCAGTGGCTC 1430
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