Tag | Content |
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EnhancerAtlas ID | HS095-30231 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr8:141655640-141656980 |
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) |
NHLH1 | MA0048.2 | chr8:141656880-141656890 | CGCAGCTGCG | + | 6.02 | NHLH1 | MA0048.2 | chr8:141656880-141656890 | CGCAGCTGCG | - | 6.02 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_44253 | chr8:141655104-141658025 | NHDF-Ad | SE_44816 | chr8:141655326-141657122 | NHLF | SE_46385 | chr8:141655005-141658265 | Osteoblasts |
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| 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 |
GH08I140644 | chr8 | 141654375 | 141657855 |
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Enhancer Sequence | CATATTTTTA TCCTAAGGAG ATATTTTTAT GTTTGAAAAT CTTATTGATT ATGCTATATA 60 CTTGTCTACA ACAAAAAGTA TATATAAATT GAAATCTGAA ATTTTTATTT CCTGTGAGAC 120 CAAGTGTTAG AAAACATTCT TCTGGGCTTA CTTATCATTA CAACTGTCAG AACACAACTA 180 ATCAAACACA AATATATTAC AAAGTTTGAA TAATAATTAT TAGTCATGAA AGTGTCACTC 240 ATTAGTCATA CATTTTTGTT GGAAATAATC TCTTAAGGAA AATAGTGGAC TTTTCTTTTT 300 CTAATTCCCA GACTCAGGAA GAACCGGATG ACCCATTGCT GGAGTCAGGG CTCTTCAACA 360 ATTCTTTTCC CGTTCCCCAT GTTTGTGAAT GTCAGTGCTT ACAGCTGCGG TCCCAGGAAG 420 CGTGGGTGAG AATGGAAGGA AATTCTGTTA CAGTGACTCA GTGCTCTGAC CCCTCCCAGG 480 ATATCCTCCA GAACTCGCAT GCTGCTCTCC TACCGACAGT CCTGGGTGAG AACCCACAGC 540 TGGCGACTCA GCCATCCTGC CTCAGGGTGA TGGAAGCTAC AACTGAAGTC ACCTGGCTTT 600 CAAAAGGTTC TTTTGTGGCC GGGCGCGGTG GCTCACGCCT GTAATCCCAG CACTTTGGGA 660 GGCTGAGGCG GGCGGATCAG TTGAGGTCAG GAGTTCGAGA CAAGCCTGGC TAACACAGTA 720 AAACCCCGTC TGTACTGAAA ATACAAAAAA TTAGCCGGGT GTGGTGGCAG GTGCCTGTAG 780 TCCCAGCTAC TTGGGAGGCT GAGGCAGGAG AATGGTGTGA ACCCAGGAGG CGGAGCTTGC 840 AGTGAGCCAA GATCGCGCCA CTGCACTCCA GCCTGGGCGA CAGAGCGAGA CTCCATCTCA 900 AAAAAAAAAA AAAAAAAAGG ATCTTTTGTG ACCCTAATTG AGTCTGGGTG TCTACAGAAA 960 GGTGTGATAG ATGAGATTAC CATCCAAAAG TCATCGCTCC CTTGCCCTTT ACAGTTGATT 1020 TCTTACCCCA GTGGCGCTGA GCTCAACCGT GTGACTGTCA ACGGTCGACA GGATGTCAGC 1080 AGTCCTGCCC TCAGAGGCTT ACATGCAGTT GCCCCGTCTG GTTGCCAGGT TGGTCTCAGC 1140 CAGGTGGCCT AGAGAAACCT TCCTCCCTGC ATCTTCCTCA GCCTGGTCGC TGAGGGCATG 1200 TGAAGCCAGG TCCATCTGGA GGCAGAGCCT CCCAGCCACA CGCAGCTGCG CCAGCTAATG 1260 CACAGAGGTG GAGTGAGGGG AACACGTGTT GTTACACAGC AGAAGCTGAG TCAAAATCCC 1320 CAAGGGGCCT TTTAAAACGT 1340
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