| Tag | Content |
|---|
EnhancerAtlas ID | HS147-00088 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:1617100-1618860 |
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 | ATCAAACAAA CGACACAATC ACCCTGAGGG GAGAAGCAGA ACAAGCCCTG GGAACTCGGG 60
TGCATGGACG CTGGATGTGG GTACGCAGGT GATGGACACA AGGGCTCCAG ACACACAAGT 120
AGCTCCAGAC ACAGGAGCTC CAAACAAATA CCGAGTTCTA AACATGCTTT TTTCCCTTTT 180
CTTTTCTTGA GACGGAGTCT CGCTCTGTCG CCCAGGCTGG AGTGCAATGG CGCGATCTCA 240
GCTCACTGCA ACCTCTACCT CCCGGGTTCA AGTGATTCTC CTGCCTCAGC CTCCTGAGTA 300
GCTGGGATTA CAGGCACCCG CCACCACGCC CAGTGAATTT TTGTATTTTC ATTTCATTTT 360
TAGATGGAGT TTCACTCTTG TTGCCCAGGC TGGAGTGCAA TGGCACGATC TTGGCTCACC 420
ACAACCTTCG CCTCCCAGGT TCAAGCGATT CTCCTGCCTC AGCCTCCCGG GTAGTGGGGA 480
TTACATGCAC GTGCCACCAA ACCCTGCTGA TTTTGTATTT TTAGTAGAGA CGGGTTTTCA 540
CCATGTTGGC CAGGCTGGTC TCGAACTCCT GACCTCGTGA TCTGCCTGCC TCGGCCTCCC 600
AAAGTGCTGG GATTTACAGG CATCAGCCAC TGCGCCCAGC CTCCCTTTTC TTTTTTTTTC 660
TTTTTTTTTT TTTTTTTTGC TGACTCATGG GTTAGAATTC CGGATTGGGC AAATACATAA 720
ATATTTTGTA CATGACGGGA GGCAGATTTC ATCATGTGAG TGAAGCGAGA TGCAAACACG 780
AAAGGAAGTC CTTCAGGGCA GTCTTGTAGT GAAAAAATAA AAATAAAAAT GAAAAAAAGA 840
GGCTGGGCAC GGTGACTCAC GCCTGTGATC CCAGCACTTT GGGAGGCCGA GGCGGGTGGA 900
TCACCTGAGG TCAGGAGTTC ATGGTGAAAC CCCATCCCTA GTAAAAATAC AAAAGTTAGC 960
TGGGTGCAGT GGCATGCGCC TGTAATCCCA GCTACTCGGG AGGCTGAGGC AGAAGAATCA 1020
CTTGAACCTA GAAGACGGAG GTCGCAGTGA GCCGAGATCA TGCCACCACA CTCCAGCCTG 1080
GGCGACAGAG ACTCTGTCTC AAAAAAATAA AAAGGCCAGG CACGGAGGCT CACGCCTGTA 1140
ATCCCAGCAC TTTGGGAGTC CAAGGGGGTC GGATCATGAG GTCAGGAGAT CGAGATCATC 1200
CTGGCTAGCA CTGTGAAACC TTGTCTCTAC TAAAAATACA AAAAATTAGC CGGGCGTGGT 1260
GACGGGCACC TGTACTCCCA GCTACTCAGG AGCCTGAGGC AGGAGAAGGG CGAGAACCCA 1320
GGAGGCGGAG CTTGCAGTGA GCTGAGATCG TGCCACTGCA CTCCAGCCTG GGCCACAGAG 1380
TGAGACTCCG TCTCAAAAAC AAATAAATAA ATAAATAAAA AGAAGAAAGA AGATGGATGG 1440
AATGACCCCC GCGGTGTCGG CCTGTGAGGG TGCTGTCGGG CCCGAGCGCA CAGGCTTGAA 1500
CGGATGGGCG GACGGGCGAC ACGCACGCAC ACACACACCC CAACACAGCA CATCTGCCCA 1560
GAGACAGTCA CACCTGCACA GCGCGCTCCC AGCGCCCTAA CCTTGGTTTC TAAATATCAT 1620
TCTCCACTAA AGGGGCTGGG CGCAATGGCT CACGCCTGTA ATCCTAGCAC TTTGGGAGGC 1680
TGAGGCAGGC GGATTACCCG AGCTCAGGAG TTCTAGACGA GCCTGGGCAA TGTGGCGAAA 1740
CCCTGTCTCT ACTAAAAATA 1760
|
