| Tag | Content |
|---|
EnhancerAtlas ID | HS102-00042 |
Organism | Homo sapiens |
Tissue/cell | HuCCT1 |
Coordinate | chr1:1617020-1619000 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr1:1617775-1617790 | TTTGCTGACTCATGG | - | 6.4 | | Nr2f6(var.2) | MA0728.1 | chr1:1618006-1618021 | GAGGTCAGGAGTTCA | + | 6.22 | | RARA | MA0729.1 | chr1:1618006-1618024 | GAGGTCAGGAGTTCATGG | + | 6.39 | | Zfx | MA0146.2 | chr1:1617982-1617996 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_13835 | chr1:1616834-1618483 | CD34_Primary_RO01536 | | SE_27558 | chr1:1617423-1618832 | Esophagus | | SE_34455 | chr1:1616569-1618227 | HCT-116 | | SE_34455 | chr1:1618494-1619079 | HCT-116 | | SE_40508 | chr1:1617417-1618219 | K562 | | SE_45385 | chr1:1616829-1617278 | NHLF | | SE_53355 | chr1:1617565-1618375 | Spleen |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 1618656 | 1618849 | | chr1 | 1617560 | 1618333 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I001685 | chr1 | 1616659 | 1618918 |
|
Enhancer Sequence | AAAATAATTA AATCAACAAG GGTAGGGGAA AAGGGTCTCT GAAATGGAAC ACGAACACGA 60
ATGCATGAAC CACACCACAG ATCAAACAAA CGACACAATC ACCCTGAGGG GAGAAGCAGA 120
ACAAGCCCTG GGAACTCGGG TGCATGGACG CTGGATGTGG GTACGCAGGT GATGGACACA 180
AGGGCTCCAG ACACACAAGT AGCTCCAGAC ACAGGAGCTC CAAACAAATA CCGAGTTCTA 240
AACATGCTTT TTTCCCTTTT CTTTTCTTGA GACGGAGTCT CGCTCTGTCG CCCAGGCTGG 300
AGTGCAATGG CGCGATCTCA GCTCACTGCA ACCTCTACCT CCCGGGTTCA AGTGATTCTC 360
CTGCCTCAGC CTCCTGAGTA GCTGGGATTA CAGGCACCCG CCACCACGCC CAGTGAATTT 420
TTGTATTTTC ATTTCATTTT TAGATGGAGT TTCACTCTTG TTGCCCAGGC TGGAGTGCAA 480
TGGCACGATC TTGGCTCACC ACAACCTTCG CCTCCCAGGT TCAAGCGATT CTCCTGCCTC 540
AGCCTCCCGG GTAGTGGGGA TTACATGCAC GTGCCACCAA ACCCTGCTGA TTTTGTATTT 600
TTAGTAGAGA CGGGTTTTCA CCATGTTGGC CAGGCTGGTC TCGAACTCCT GACCTCGTGA 660
TCTGCCTGCC TCGGCCTCCC AAAGTGCTGG GATTTACAGG CATCAGCCAC TGCGCCCAGC 720
CTCCCTTTTC TTTTTTTTTC TTTTTTTTTT TTTTTTTTGC TGACTCATGG GTTAGAATTC 780
CGGATTGGGC AAATACATAA ATATTTTGTA CATGACGGGA GGCAGATTTC ATCATGTGAG 840
TGAAGCGAGA TGCAAACACG AAAGGAAGTC CTTCAGGGCA GTCTTGTAGT GAAAAAATAA 900
AAATAAAAAT GAAAAAAAGA GGCTGGGCAC GGTGACTCAC GCCTGTGATC CCAGCACTTT 960
GGGAGGCCGA GGCGGGTGGA TCACCTGAGG TCAGGAGTTC ATGGTGAAAC CCCATCCCTA 1020
GTAAAAATAC AAAAGTTAGC TGGGTGCAGT GGCATGCGCC TGTAATCCCA GCTACTCGGG 1080
AGGCTGAGGC AGAAGAATCA CTTGAACCTA GAAGACGGAG GTCGCAGTGA GCCGAGATCA 1140
TGCCACCACA CTCCAGCCTG GGCGACAGAG ACTCTGTCTC AAAAAAATAA AAAGGCCAGG 1200
CACGGAGGCT CACGCCTGTA ATCCCAGCAC TTTGGGAGTC CAAGGGGGTC GGATCATGAG 1260
GTCAGGAGAT CGAGATCATC CTGGCTAGCA CTGTGAAACC TTGTCTCTAC TAAAAATACA 1320
AAAAATTAGC CGGGCGTGGT GACGGGCACC TGTACTCCCA GCTACTCAGG AGCCTGAGGC 1380
AGGAGAAGGG CGAGAACCCA GGAGGCGGAG CTTGCAGTGA GCTGAGATCG TGCCACTGCA 1440
CTCCAGCCTG GGCCACAGAG TGAGACTCCG TCTCAAAAAC AAATAAATAA ATAAATAAAA 1500
AGAAGAAAGA AGATGGATGG AATGACCCCC GCGGTGTCGG CCTGTGAGGG TGCTGTCGGG 1560
CCCGAGCGCA CAGGCTTGAA CGGATGGGCG GACGGGCGAC ACGCACGCAC ACACACACCC 1620
CAACACAGCA CATCTGCCCA GAGACAGTCA CACCTGCACA GCGCGCTCCC AGCGCCCTAA 1680
CCTTGGTTTC TAAATATCAT TCTCCACTAA AGGGGCTGGG CGCAATGGCT CACGCCTGTA 1740
ATCCTAGCAC TTTGGGAGGC TGAGGCAGGC GGATTACCCG AGCTCAGGAG TTCTAGACGA 1800
GCCTGGGCAA TGTGGCGAAA CCCTGTCTCT ACTAAAAATA CAAAAAATTA GTCTCTACTA 1860
AAAAAACAAA AAATTAGGCC GGGCGTGGTG GCTCACGCCT GTAATCCCAG CACTTTGGGA 1920
GGCCGAGACG GGCAGATCAT GAGGTCAGGA GACCAGCCTG GCCAACATAA TGAAACCCCA 1980
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