| Tag | Content |
|---|
EnhancerAtlas ID | HS146-01390 | Organism | Homo sapiens | Tissue/cell | NHDF | Coordinate | chr1:232278070-232279570 | 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 | AATAAAAAAC AGAAAAAAGT AATGCAAGCC AATGTGGAAA TAAGTATAAT CCAGAAAACA 60
ACCATGAAGA AAGGATCCCA TCCAGACTAC AGGGAACAGA CTGAGAGACC TCAGTGGCTT 120
CCAGTTGCTA ATGTGTGTGA TTCCCACACT GGGTAACACA GGAGTGTTTG ACCAACAATC 180
AACTGAATAC TGGTTCTTGT TTCTCATTGT CATGGAATTT GCCGAATCTC ACTTTTGGCT 240
TCACAGAGGA CTTTGTGAGC TCCAAGCATG AAAAGTGGCA TTTATAACTC CCCCTGGAAT 300
TTCCATGTAC CCAGGACACT GCCAGGCCAA AGGATGAATC ACAGCTTCTT AGAATTGTGG 360
AAGCCATTTT GGAAACAGCT GCCAAGTAAC TAATGCTATT AAAAATAGCT CCCTAAAAAA 420
TGAATTGCTT ATTTTAAGAA GACAAGAGTG GCTTGAATCT GTGCTGCTCA CATTTTTCAT 480
CTACTGGGCA CAGTGCCCGT GGATCCAAGA AAGCCCTGCT TGTCAGATGG GAATACCATC 540
TGTACAGATG ATGCCCCGCA CATGCAAGAG CCTGGCATTT TTGGGCCAGG GCTAACCAGG 600
GTAAAGTCTG AATCACCCCA TGTGGAATCC GTCTCCTACG GGGTGTGGAC TGTGGGGCAT 660
GAATTCCAAT TGCGCTTTCC TTACATAACT TTGCTCTTCA GATCCCTGGT TCCGAATGTG 720
GGGTGTATGC AGTATGGCCC ACTGGAAGTA CATGAAAATG CTAGAAGGTG AATCTACATG 780
TATTTTTTGA TCTAATGAAA ACAAGCAGGA AAATAAGTTG TACTGACAGG TAATGTGCAG 840
ACTGATACTG CTGTCTTGAC TCAGACTGTG TTGGGCAATT GTCTTTCCCT GTGAATTCCG 900
TGAAGAAATG AACCCATCCA GACCCATCCC ATGGCAATAG GATTGATGGT GCCAACCTCC 960
CATGTTTGTT TTATGCCCCC TGTGTTGTGA CGTGGGGCAG TTAACCTATT TCTGGCTTAA 1020
ACAGTGTCAA AAATAAACAA AGCCAGGCAC TAGTTAAAGT GGTAAGAAGA GACTTCAATC 1080
AGCACTTTGA TTTGTGCAGC AGTGACTAGG CATTTTAAAG GAAGAATAAG GGAATGAGGA 1140
GAGGTGTGAG TGGGGACTCA GGAGAGTCAG GGAAGTGAAA AATCATCAAA GGCGGGAGGG 1200
AGGAAGCTTG GTCCATGTGG AAACTATCTG GATTTTCTAA GTGCTCCTTC TCAAAGCGCT 1260
GCCCTTCTGG AGGCTGGGAG ACAGGGTACT TATCTTCAGG TTTTGGCTGA AACAAACAGT 1320
AAATTCCTTG GGCAGCCCTG CATTTCTCAG GCAGGCACTT TAAGGAGATT AGGGGCATGC 1380
TAAGGATGTG GCCTTGAGCT GCTAGAAACT GTGTTTGTGT TTGTTCAAGC CTTTATAGGC 1440
CAAGGATGAG GCCTAGTGGA GAAGGGGGCT CAGTGGAGCC TGACTAGAAT TTGGTCAAGA 1500
|
| |
|
|
|
