Tag | Content |
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EnhancerAtlas ID | HS138-02479 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr1:159566400-159569020 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NEUROD2 | MA0668.1 | chr1:159566429-159566439 | ACCATATGGC | - | 6.02 | RORA | MA0071.1 | chr1:159567589-159567599 | TGACCTTGAT | - | 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 |
GH01I159596 | chr1 | 159566407 | 159569121 |
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Enhancer Sequence | ACACACACAC ACACATGCAA ATATTCCTAA CCATATGGCA GCATATCATA GTATTGTTCT 60 CTAAATAGCT CGTTTTGTGG TTGTTATTTA ATGTATTCCA CACATCTGTT CATGGTAGGA 120 CACCATAACA GCACAGTCCA GCATAACTTT TACCAACAAA AGAAAATGTT TGATAGCTGA 180 GCTATCCAAT ATGGTGGCCA CTAGTCACAT GTAGCTTTTT ATCACTTGAA ATGTGGCTAG 240 TATGACCGAC TAAGTGAATT TTTAATTCTC TTTTATTTTA GTTAATTTAA ATTTACACAG 300 CCATAGCTCC ATCCTATCCT TTCTAAAAAG CTGCTTGGAG TTCCACTGTC ACTCTCTTTA 360 ATCTTTGCCT ATCCAACTGG TATCTCAGTG GTCTCTTAAG GCAAATTCCT TTAATTTTAG 420 TGACACACTC ATTTCTACTC GAAACATTTG CCTCATTTTC CATGATGGAC TATTTTCTAA 480 AACACCCACA ATATTTCCTA GATTCCTAGT GGCAGTTCCC TAAGTGTGCC AAAATCCCCC 540 AGCCTGTTAG TGTTACTTGT TATTTAAGCA AAATGATTCA AATCATCATT TGATACATGA 600 TGGAAATCCC AGGCTCACTC ACCAAATTTC TAGCAAATAT TGTGTGTGCT TGTAAGGGGG 660 ATGGGAGGGC AGGAGAAGGC CTTGTATTTC TTCTAGTCAT TACAAGCTAG TGGTTTTTCT 720 TCCTCAGTCT GGAACTTACT CCTTGCACAT ACCTTTTTCT GCACTGTGCC ATCATCCACT 780 TCTCTTTACT TCCTAACTAC CACCAACTGA AAATTATACA TATAAAAGCT TTAAACAAAG 840 TCTCTTGAGG CTCTCAAGGG AGTTTACATT ACAGTATAGT TCAGCAAACA ATTTTAAATC 900 AAATAGTACA CCTCTTTATT CTTAGAATTC CCTCTGCCAA AAAAGAAATC AGCTACTTTT 960 TTTTAAATTC AAGGTCCAAC TTTCTGTTGT GTTGCTGATT CTCTTCTCTC TTTTTCCAAC 1020 GACTTCCACT TCTCTCTCTA GTTTACATGT CTCCAAACCT TAAGCCTCTG TTAATACTTT 1080 CACAATAAGT CAATTTTGCC AACGGTTTGC CTCCCCTAGA CCATCTAGGC TGGGCCCAGA 1140 ACACCTCATC TTCACTCCCA CTGAAGTGTT CCTGAAGGTC AGCTCTCACT GACCTTGATT 1200 CTGCTCCCCT ACACTGTCAC CAGAAGCTAT CCACCTATGG TTCTAATTCA GTAAGTCCAA 1260 CTCTCTCACC CCCTTTTTTT GTCTCAGCTG TGTGGGCTTT CCCAGGATGG CATGCAATGG 1320 GACCCCTGTG CCATGCATAT TGTAAAGGAA AATGCCTCCC TCCATGCGCT ACAAAACAGC 1380 ACATTTATGA TGGCACTTTG AAAAGATATG GGTTGTGGTG TCACATATTG ACAATTCCTT 1440 GGCCAGAGGC TTAACAGTGC CAGCAGTGCC AGAAGATTAA GAAGACAGCA AAAACAGAAA 1500 AGGGAGAAGA TGGTGAAGTA GTTATATAAC ATGAGCGAGA ATGCTCCTGA TTACAAAGCA 1560 GAGAAATTGA CTTTTTTTCT TAGTGTTTTC TATAGTCATT GCTCTATCCC TGTTCTAGAA 1620 TTCAAGTCAT GATAAGAATT TCTTCACGTT GACTTCCTGC ATTGCTTTCA GACATTGCAA 1680 TTAAAGAATG CGAAGAAAGA ACCTCACAGA GGTAACAGAG TTTGTTTTCC TGGGATTCTC 1740 CAGATTCCAC AAACATCACA TCACTCTCTT TGTGGTTTTT CTCATCCTGT ACACATTAAC 1800 TGTGGCTGGC AATGCCATCA TCATGACCAT CATCTGCATT GACCGTCACC TCCACACTCC 1860 CATGTACTTC TTCCTGAGCA TGCTGGCTAG CTCAAAGACA GTGTACACAC TGTTCATCAT 1920 TCCACAGATG CTCTCCAGCT TCGTAACCCA GACCCAGCCA ATCTCCCTAG CAGGTTGTAC 1980 CACCCAAACG TTCTTCTTTG TTACCTTGGC CATCAACAAT TGCTTCTTGC TCACAGTGAT 2040 GGGCTATGAC CACTATATGG CCATCTGCAA TCCCTTGAGA TACAGGGTCA TTACGAGCAA 2100 GAAGGTGTGT GTCCAGCTGG TGTGTGGAGC CTTTAGCATT GGCCTGGCCA TGGCAGCTGT 2160 CCAGGTAACA TCCATATTTA CCTTACCTTT TTGTCACACG GTGGTTGGTC ATTTCTTCTG 2220 TGACATCCTC CCTGTCATGA AACTCTCCTG TATTAATACC ACTATCAATG AGATAATCAA 2280 TTTTGTTGTC AGGTTATTTG TCATCCTGGT CCCCATGGGT CTGGTCTTCA TCTCCTATGT 2340 CCTCATCATC TCCACTGTCC TCAAGATTGC CTCAGCTGAG GGTTGGAAGA AGACCTTTGC 2400 CACCTGTGCC TTCCACCTCA CTGTGGTCAT TGTCCATTAT GGCTGTGCTT CCATTGCCTA 2460 CCTCATGCCC AAGTCAGAAA ACTCTATAGA ACAAGACCTC CTTCTCTCAG TGACCTAAAC 2520 CATCATCACT CCCCTGCTGA ACCCTGTTGT TTACAGCCTA AAGAACAAGG AGGTCAAGGA 2580 TGCCCTATGC AGGGCCATGG GCAGAAACAT TTCTTAATGC 2620
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