Tag | Content |
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EnhancerAtlas ID | HS095-17102 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr2:145077730-145079280 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LHX2 | MA0700.1 | chr2:145078974-145078984 | GTTAATTAGT | - | 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 |
GH02I144320 | chr2 | 145077721 | 145078661 |
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Enhancer Sequence | ACATGGCTAT ATTCTTTCAT TTAGGTATGC TTCTACAGCT ACTTTCAGGC TATAGTGGCC 60 AACTTGAGTA GGTGCAACAG AGTCCATAGG GTCCATAAAG ACTAAAATAG TTACTGCCTG 120 GTCCTTCCAA GGAGAAGTTT GCAAACCCCT GGCCTAAATT ATTTTTTTGG TGAGTAGGTA 180 ACATGATACC TAGTGTATGT CACATGAAGA ACCTAAGTGG AAAGACTATA ATGTTTCCCT 240 GTCTTACTTC TATCCATTCA ACTAACAAGT ATTTGTTTGG CCAGACCTGT TACTACAATG 300 CAGACAGCTC TAGTCACTTT GGTCTCCCTT TTGGCTCAGT TTTGCCTCAA TCCAAGGGGT 360 TAATATTGAC TTTGGGCAGG AAGAGGACAA GGAGCTCACC TTCAGGTCAA ATTCCAGTTC 420 TCCAACTTTG GCCTGCTCCA TGTCCCCAAA CTCTCCTGGT TCTGAATTTC TGCTTTATAT 480 CAACCATTCT CTGTAATGGA CTTCCTGTAC TAGACATCAG TCTAGTCTGG CAGTATTTCC 540 TGCCAAAGAC ATGTGGGCAA GGGGCTGAGT CACGGCATTC TTTGAACTAT GCCAGCTGAT 600 CATCAGTTCT ATGCCTGCTC TAACAGCCAT CCTGCATGGT GGATTTGTTT TGGGCACCTT 660 GTGAACAGTC TGCATATTCC AACACTCCTC TTGGCTTCCA CTGTTCCTCC TGGTTATGAT 720 TGCCCCTGAA GTTCATCACT TTCATTTTAC ATTGAAACTT CTGGCCAAAG ACTTGTTCAA 780 CATTCCCAAC TGGCCTGTCT TTTTGTTATT TGAGTTCAGT TCATATAACA AGAGACCAAG 840 AAAATTTTAT CTATATAGAT GGATTTCCCA ACTTAGAAAC ACCCAACTTA AAACATCTCT 900 TATGTTTTAG CATCTGCTCC AAAAGAGAAT ATATCACCCC CCACAACCAA GTAGTATCCA 960 GAATATCCGT TTTTTCCCTC CAACACTGCT AGTTGGCCCA AAGTTTCTAT ACTTGCTTCA 1020 TCTGAAAGCG TTACCTATCA CCCACCACCC ACGTGGGATG CCCAAGATAT CTGTGTCTCT 1080 TGAGCATTGC TTCAAAACGC CTCTCTTGCT GTCACTAAAG CTTTAACAAC CCTGTTTCTG 1140 TTGTGAGGGA AAAAGAAGAG TTTCCTGCCA CTGCTGGACT GCAATGGAGG AATGTGTTTG 1200 GCTAGATTTC TAGAAGTCAA AAGTATAATT CCACACAAAA AGATGTTAAT TAGTCCATAA 1260 TGAGGCTGAA ACACTCATAC TATTAATGGC ACTACAGAAC CCATCTGTAA TTCATATTAC 1320 ATTGTTGCAG ATAGTTAATT CACAAACGCA GTCATAAATT GTAGATTGAC GGTACTAGAA 1380 AATAGCTTTA AAAATGTCAG GACGGATTAG CGTATGGACT TCAAAGAAAA TTGGTTTATT 1440 ATTTGTTTAT TTGATTAAGA GACAGAGTCT CACTCTGTCA CCCAGGCTGA ATACAGCAGC 1500 ACAATCATAG CTCACTGCAG CCTCAAATTC CTGGGCTCAA GAAATCCTCC 1550
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