| Tag | Content |
|---|
EnhancerAtlas ID | HS059-04101 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr1:212922350-212924030 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:212923355-212923374 | GGTCCACTAGAGGGCAGTA | + | 6.79 | | EBF1 | MA0154.3 | chr1:212923417-212923431 | ACTCCCTTGGGAAC | + | 6.18 | | MEF2C | MA0497.1 | chr1:212922411-212922426 | TTCTATTTCTAGATC | - | 6.12 | | MSC | MA0665.1 | chr1:212923097-212923107 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr1:212923097-212923107 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr1:212923097-212923107 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr1:212923097-212923107 | AACAGCTGTT | - | 6.02 | | RELA | MA0107.1 | chr1:212923765-212923775 | GGAAATTCCC | - | 6.02 | | SOX10 | MA0442.2 | chr1:212923976-212923987 | AAAACAAAGCA | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I212749 | chr1 | 212922781 | 212924141 |
|
Enhancer Sequence | AAATATAATC AATATACTGT TTAAAAATAA GTTTATCCTA TATTTTCCAA CTATGCAGAT 60
ATTCTATTTC TAGATCATGG TGGCAGTTAC ATGTGTGTAG GTGTATGCAT GTAAATAAAT 120
TCATAAAGCT GTGCATTATA TGTTATACTG CAATATATGT GCACACACAC ATACAATAAT 180
GAACAAAATA TTTATTAACA TTTAATATGA AAAGTTATCT TTTATGAATA GGGTAAGGTA 240
AAATCATATT CTTCTTCATT GTTATTATAT TGTTTACATT ACAAACTTTA CAAAATAATC 300
CATCACTTAA GGGATTTTGC GTTTTATTGT GTTTTTTTTT TTTTTTTTTT TTTTGAGACA 360
GGGTCTCGAT CTGTCACCCA GGCTGGAGTA CAGTGATGTG ATCACTGCTC AGTGCAGCCT 420
CAAACTCCTG GGCTCAAGCA TCTCACTCTG TCACCCAGGC CGGAGTGCAG TGGCACGATC 480
ATAGCTCACT GCAGCCTCAA ACTCCTGGAC TCAAGCAGTC TTCCTGCCTT AGCCTCCCAA 540
AGTGATGGGA TTACAGGTGT GAGCCACTAT GCCCAGCCTA CACTTTATTT TTTAATTAAC 600
AGCACTGATA ACCATATTCA CTGATTTGTG AAGCCTCTCA CTAGGATTCT TAGAGACTAA 660
GCGCCATCAA TGACCAATAT AAAGAATTCT TAAAATATCT CATGCTACCT TAAAAAGAAA 720
TTTGTCTCTA AACTCACATT GCTGAACAAC AGCTGTTTTC TATCGGTTGC ACAAGCAATG 780
ACAATGTAAA AAGTGCTAAG AGTAGTTTGG GTTTGTGTGT AAAATGGAAT TAGGTCCTAG 840
GCTGAATAAT TATAAACATA TTTTAACAAA TGAATGTCTA GTGAGATATC CTAAAGTTGT 900
GCTGGACATA TGAGACATCT AGTATGCCTG GCCCCTGACT ACAAAGTGCC AGCTACACTT 960
TCCCATTAAT ATGGCAACCA AAAACTTTCT TTCACTTTTT CAAAGGGTCC ACTAGAGGGC 1020
AGTACTAACC CCAGTGAGAA CCCTGGCATT CTCATTTAGC TTCCAGAACT CCCTTGGGAA 1080
CAGGAAACAC ATTCTTTTAA TCTCAGAATC CCTAATGTTG AACAGAGTGC CTAACGTGTA 1140
CAGTAGGTGT TCAGTAGTCA TGATGGACCA AGGCTATGAT AGAGGGTGCC ATGGAGGCAC 1200
AAAGGAGGGT GAGATCAATC TAACAAGGGA ACCGAAGGGA GAGGGAAATC TTCACAGGTG 1260
ATGTAAGAAA GTTGCCTTAA TAGAGGATTT GGGGCTAGGT GAGCTGGGAG GAGGTGGGTG 1320
GTAGAGGATG TGATACATCA AAGACAAGAG AATAAATCAA GAAAGAGTAG AAAACAGGAA 1380
CCAGGAAACA CGATTTAAAA CATGAGAGAA GGAAGGGAAA TTCCCAGGAC GATGATGAAA 1440
GGAACAGGCA GGATGAAAAT TTTGCACCAG GCCTAGACAG CAGCCAGTCC AGACTGGAAT 1500
AGGAGGACAG AAGGTTCCCA GAGAAGTATC TCCGAGGAAA AGATAAAGTT TAAAAATGGA 1560
TCTGAGAGAT AACCTTAAGT GTTTGCCATA TTGAGATGAA TTTTACAGTT CTGTTAGACA 1620
CAACAGAAAA CAAAGCAAAC AGAAAAATAG GCCAGGTATG GTGAGCCACA CCTGTAATCC 1680
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