| Tag | Content |
|---|
EnhancerAtlas ID | HS148-01763 | Organism | Homo sapiens | Tissue/cell | NHLF | Coordinate | chr1:232278140-232279260 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SREBF2 | MA0596.1 | chr1:232278681-232278691 | ATCACCCCAT | - | 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 |
| GH01I232142 | chr1 | 232277824 | 232279897 |
| Enhancer Sequence | AAGGATCCCA TCCAGACTAC AGGGAACAGA CTGAGAGACC TCAGTGGCTT CCAGTTGCTA 60
ATGTGTGTGA TTCCCACACT GGGTAACACA GGAGTGTTTG ACCAACAATC AACTGAATAC 120
TGGTTCTTGT TTCTCATTGT CATGGAATTT GCCGAATCTC ACTTTTGGCT TCACAGAGGA 180
CTTTGTGAGC TCCAAGCATG AAAAGTGGCA TTTATAACTC CCCCTGGAAT TTCCATGTAC 240
CCAGGACACT GCCAGGCCAA AGGATGAATC ACAGCTTCTT AGAATTGTGG AAGCCATTTT 300
GGAAACAGCT GCCAAGTAAC TAATGCTATT AAAAATAGCT CCCTAAAAAA TGAATTGCTT 360
ATTTTAAGAA GACAAGAGTG GCTTGAATCT GTGCTGCTCA CATTTTTCAT CTACTGGGCA 420
CAGTGCCCGT GGATCCAAGA AAGCCCTGCT TGTCAGATGG GAATACCATC TGTACAGATG 480
ATGCCCCGCA CATGCAAGAG CCTGGCATTT TTGGGCCAGG GCTAACCAGG GTAAAGTCTG 540
AATCACCCCA TGTGGAATCC GTCTCCTACG GGGTGTGGAC TGTGGGGCAT GAATTCCAAT 600
TGCGCTTTCC TTACATAACT TTGCTCTTCA GATCCCTGGT TCCGAATGTG GGGTGTATGC 660
AGTATGGCCC ACTGGAAGTA CATGAAAATG CTAGAAGGTG AATCTACATG TATTTTTTGA 720
TCTAATGAAA ACAAGCAGGA AAATAAGTTG TACTGACAGG TAATGTGCAG ACTGATACTG 780
CTGTCTTGAC TCAGACTGTG TTGGGCAATT GTCTTTCCCT GTGAATTCCG TGAAGAAATG 840
AACCCATCCA GACCCATCCC ATGGCAATAG GATTGATGGT GCCAACCTCC CATGTTTGTT 900
TTATGCCCCC TGTGTTGTGA CGTGGGGCAG TTAACCTATT TCTGGCTTAA ACAGTGTCAA 960
AAATAAACAA AGCCAGGCAC TAGTTAAAGT GGTAAGAAGA GACTTCAATC AGCACTTTGA 1020
TTTGTGCAGC AGTGACTAGG CATTTTAAAG GAAGAATAAG GGAATGAGGA GAGGTGTGAG 1080
TGGGGACTCA GGAGAGTCAG GGAAGTGAAA AATCATCAAA 1120
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