Tag | Content |
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EnhancerAtlas ID | HS145-13138 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr2:119007000-119008310 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TBX21 | MA0690.1 | chr2:119007252-119007262 | TTCACACCTT | - | 6.02 | TBX2 | MA0688.1 | chr2:119007251-119007262 | TTTCACACCTT | - | 6.62 | Twist2 | MA0633.1 | chr2:119007332-119007342 | ACCATATGTT | + | 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: 2 | ID | Chromosome | Start | End |
GH02I118252 | chr2 | 119007201 | 119007350 | GH02I118249 | chr2 | 119007362 | 119008298 |
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Enhancer Sequence | CCCTCATCCT GCCCACCCCG CACTGCCCCT GCCAGCTCCA GGCGCTTCCC GCCTCATGCT 60 CTCCTAACTT ACTGCTCTAA CTCTCATTCT CCCCACTCAC ATCCATCCTA CACTCCCTAA 120 TCAGCATCCT CTTCTCAAAG TGCAGCTCTG CTCAAGTCCA TTCCTGCCCC AGAAGCTTCC 180 CTGTCACATG CTGAATAAGG CACAAGCTCA CACCCCAGAA ACAGCCTTTC CCCAGGAGGC 240 CGCAAACTTC CTTTCACACC TTCTCTCCGT GCTTTCTCTC CAGTGACCCA AACTGAACCC 300 TTGACTCATT TAACAAATAT TTTGAGGAAC TTACCATATG TTAGGCATTG TGGTGGGATC 360 GCACACACAA GAAGTTTTAA AATGACCTGA ACTGCCTTCA CGTTGTTCAG GGTTTAGTGG 420 GGCAGATATG AGACAGCAAT ATTCTGTGCT AAGTGCCGTC GGGGGTGAAT GCCTAGGGTG 480 CTGGGGGAGT ATGAGGAGGG GTAGTTAACC AGCCCAGAGC AGTCTGGGAA GGCTTCCTGG 540 AAGAATCCTG AAGAAATCAG CACTCACCAC CTCCCAAGTA GCACTCTCTG CCTTCTTGTT 600 CATGTGTTTT CTTCTGGATT GAGTGTCCCT GGCATATCTA CGCCTTCTGA AGTTTATTCT 660 TTGTTCAGGA CTCATTCAAA CCACCTCCTC ATCCAAGAGT CATCTCTGGA TTGCTCAACT 720 TGAAGACAGC TTCCTTTATT GACTCCTGGT GGTATATTGT ACATAGTCTT GCCTCTCGTG 780 GTTCTTTGCC TTGTCTCACT CTGCTTTTTT TATAGTTTAT TGACGTCATT ATCTCAATAT 840 CTTCAACCTT ATGTTTTATT CAGTATCCTT TTCCAAGCAT AGAGCTTTAT ATAGCTGCCC 900 TGATGCTGCC TGAATTAACT GCTTTGCGCA TATGTCCCCC TAAAGAGGAC CAGGAGCTGC 960 CCAGGATGGA TTTGAAGGGA AAGTGGAGTC AGGCTTGCTG AGCCTGGTAC ACGGTGTCAG 1020 AGAGCTCAGA GCCTGAACTT CATCAGGCCG AGGTCATGCA TGGTCACCAT ATGACCCAGT 1080 GATCTTGGCC AGGAGTCCTG GTCTCAGTCT GGGTCCCAAC GTTCATCTTT CAAGTGCAGG 1140 CCCTTGGTCA CAAAACCATC ATCTGTAGGA AAATGCAGAG GGCCCACAGT ACAGGAGAGA 1200 CGAGGTCGGG AAACCAGGAT TCCAGTGCCA CCTGTCACTT CCTGTTGAGT CACAGCATAG 1260 ATCTTCACCT TTGTTTCCCT AGTTGCAAAA TGTCAGTTTT GAATTAAGGG 1310
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