Tag | Content |
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EnhancerAtlas ID | HS138-18310 | Organism | Homo sapiens | Tissue/cell | MSC_BM | Coordinate | chr18:61664050-61665630 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr18:61664541-61664552 | TGGGTGTGGCT | - | 6.14 | SP1 | MA0079.4 | chr18:61664539-61664554 | GGTGGGTGTGGCTTA | - | 6.01 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GCTGTCTCTG CCCCAGCAAA TAAAAAGGAT GCCCAGTGAT TTGTGGGCTT ATTCATCTAC 60 TGTTACTGTC ACATTTCCCT TGTGGGGATT TTGATGGGAC CCAACTAAGA GGTTACTAGA 120 AAAGGCTGCT ATGTTTCAAT GGGGCCCATT CAACAGGCTA CCACAGCCAT CCAAGTACCC 180 TCCCTTCCCC TGGACCCCAT GGATCCACAT TTGCCATTCG ACTTACAGGT CTCAACAACA 240 TTTCAGTTCC TTTACTATCG CTCATAGTAG AAAAATAACA TCAGACACTT GTTGGGTTTT 300 TCAACTTATA AGATCCTGGA GTCAGCTGAA AGGGAGTCAG CCAAAAGGCA CATACACTTT 360 GAGAAACAAT TATTGTCCTG TTATTGGGCC TAGGTAGATA TGCATGAGTA CGTGACTCAC 420 GGCTGTGACA TAGTTTTATG ATCCCAAATT CCAATCATGT TATGAGTGAG CAGAGGCCTC 480 AAATATCCAG GTGGGTGTGG CTTAAGAGTA TTCTCTAGTG AATGAAAATG TTCTACACAG 540 AAGCAGGTAA AACCCAGCCC AGCTGGGGCC TTCAACTCAA TGGCAAGGAC TCAGGAGTGT 600 TGTCCCCCTC CCAGGCATGT CGTCCAATGA GCCACTGCCT TCACTTGGCC AATGGGAACT 660 CAGATACAAG GACCTTCTGG GCCACACATA AGCCTGGTTC ACTGACGGTG TCTCTTGATT 720 AACATTTACT ATGCTGGAAT GAGGTGCAGC TGTCATACAA CCTGAGATAG ATCTATCCCT 780 TGGCAAGTTC AGCATAAATG TGCAAAGCTT TATAAAGTAT GGTTGGCTAC CCAGGCTCCC 840 TCAACAAAGG AGCCCTGCTA TATTTTCACT GACTCATGGG CTGTAGTTAA TGGTCTGAAC 900 ATTTGATTGA GCTACTGGCA AAATTGTGCT GACATGTAAA ACACATCCCT CTCTTGGGAT 960 GAGACATTCG GATAAAATTC AATTCTACTC CTAATAAGCT CTTTGTTATC CTTGTGGGTG 1020 CTCACCAGAG AGCTCCCTAT GCTGACAAAG GCAATGAGCC AATCAAGGCA ATGAGCAGAC 1080 CGTGCATGTC AGCTAAACAT GGAGAATGAT TTGTCATCTG CCCCAGAGAT AACAGATATT 1140 CAACTCATTG CCTCTGATCC ATGAGAGGAA GGGCCCTGGG AATCAAGATG CCATCCTAGC 1200 CTGGATCTGT ATGCATGAAC TATTATCTTC AAAAGATGCC AACACAGCAT GAAAAAGATA 1260 ATCCACCCGC CAGACCCTGA GCAAGGCTAA ACATTCTGCT CAGGGACAGA TCCTTCTGGT 1320 CAAAAAGGCC AGGATGTTCT TTGCAGGTTG ATCACACTAG TCCCCTCATC CCATCCAGAG 1380 CATTCTGCTG GATCCTAAAT GTAGTTGATG AGTTCTCTGT ATTTGGACTA GTCATCCCCA 1440 TGTGTTTCCC TGACTCAGGC AACACTCTTC AGTCCCTCCA AAACCATATT TGTTTATTTC 1500 TCTGGCTTCC TGAATACATT GTATCTAATA ATGGCCCAAA CGATACATTT GCAGCCCAAA 1560 CTATACATGG GTCAAATTAT 1580
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