Tag | Content |
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EnhancerAtlas ID | HS145-15697 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr22:26812330-26813800 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr22:26813074-26813085 | GGTGACTCATG | + | 6.62 | FOSL2 | MA0478.1 | chr22:26813073-26813084 | GGGTGACTCAT | + | 6.14 | JUNB | MA0490.1 | chr22:26813073-26813084 | GGGTGACTCAT | + | 6.32 | JUND | MA0491.1 | chr22:26813074-26813085 | GGTGACTCATG | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I026416 | chr22 | 26812481 | 26813547 |
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Enhancer Sequence | CTTTGCCAGC AAAAGACTCG GAGGAACATT GAGTACACAG CCTCTCAGTT CTAGGTAGGT 60 CATATGTGTC AGCCAGTAGG TTGAGTTTAT AACAGTCACG TCGTGACCTG AACACCCTCC 120 CACTCCACTG CTGAATCAAC TAGATAGAAT CTGGCAGGGA TGATATATAA CTACCTTAGA 180 CAGGTGTAAG GGAGGGGAAA ATACAGACAA AAAGACAACA AAAAGGAAGC TTGCAAGAAA 240 AACGAAAAAA ACTGAACTAA CCCCTAATGC ATCTGATTGA GGCTTCTGCA AAACTACCAG 300 ATGCATTCAG ATCAAACTAA CTATTAAGAA ATGCAAAGAA TTGGATGCTG TCTTAGGTTG 360 AAACAAATCA AAACAAAAAA GAAATGCAAA GAAAACTTAG CTCCTTGGAG CTGTCCTAAA 420 TTCATATACC ATGCTTGAGC TTGTAACATT GATCCAGGTG ACTCCCAGTT ACGGTGTTCA 480 CTTTGTTCCC TCTAGGTATG TGCCAGGTGA TGAGGAGACA TACTGTCTGG GCTCTTCAGA 540 CAGGCTTCTT TCTCCCTGGA ACTCAGAAAA TTCCAACTAC CTAGAGTTTG CAAAGGCAGC 600 CGGCCAGGGA AGGATGCTGG CTCCAGGTCC TGGGGCCCCT CCCTGGAGGG AACAAATGCC 660 TCTCGGATTG CAGCTGCAGA AAGAGAGAGG AGAATCGGGG AATGGAATGG TGTGCTGCAG 720 AGGCAGTGGT TTGGACAGCG ACTGGGTGAC TCATGCCCCA GGCAGCTTTT TACAGGAGTT 780 GCAAATTCCA GTAATAGCAG ATCAGGAACA TCTCTCGAGG GACACCCTAC CAATCGAAGG 840 TGTCTCTTGC ACCATCTTGG CAGCGCTGAA TGGGCATCTG AATAGCTTAT CTATTCAGAT 900 CCTTTGCCGG ATCCCAAAGG TTCTCCTTGC TTTGGCCCCT GGGCTTCCTG AAACCGGGCG 960 GTTATTCTCC CCGGAAGTTG GAGGAATTGG ATAATATTGT CTACAGACAC CACACCTGAA 1020 TCTTATCCCT ACTACTACAA ATAGGGATGC TATTTTCTTG TCCTGTGTCC TGGATGGTGA 1080 ATTGAGTATC TTGTGCCCTG CCAAAAGCCA CTCTATGGCC ACCTCCTCTC TGTCCTAGGT 1140 TCCTGGAGGC TAACTGTGTA GCTCCCATCA ATGAGCGTCC TCTCTCTGGC TTTTAGTTAG 1200 GTATACTCTA CAGGCAGCCC CGGCAGGAAA TAAAAAGGTG GGAGGAGAGT GAGGTCATTT 1260 CTTCTGGCTT TCTCTTTGTG GAGTTACCAC AAGCTGACTG TGTCCCTTAT GAGAATAATC 1320 CAGCCCTCTC TAAACAATAT GGGTCTCTCC AGGTTCTGGT AGCCACTCTC CAGGTTCTGG 1380 TAGCCTTCCT TTGTCCATTC AGGCCCAAGG GGATGACATC TCCCCTGTTC CTAGTCTCCG 1440 CCTGTTACTA GTCTGTTATT AGTCTGGGGT 1470
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