| Tag | Content |
|---|
EnhancerAtlas ID | HS092-01615 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:53776420-53778090 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYC | MA0147.3 | chr1:53777639-53777651 | AGGCACGTGGCC | - | 6.07 | | ZNF263 | MA0528.1 | chr1:53777302-53777323 | TCTCTCTCTCCCTACTCCTCT | - | 6.44 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 53776578 | 53776628 | | chr1 | 53776668 | 53777368 |
|
Enhancer Sequence | AGGAGTGAGG CCTCCATCCC AGGAGGTATG CAAGCAGGGG GATCCATTCA TTCATTCAAC 60
AAGCATACAA TGGGCCCCTC CTCTGTGCTG GGCCCTGTGA TGGGCACTGG GGGGTTGGGA 120
AAGAGTGCAT GAAAGCCAGT CCTGCCTGAA GAAAGCCATA CTATAAAGAC ACAGGAGATG 180
ACAAAGGTGC CAAATCGACC CCGGGTCATG CCTGCCCAGC CCTGCACATG CTTCAGAGCC 240
CGGAGGAAAT GCAGGAGGCC CTATGCCATG AAAAGGGGCT TGGGAAACAT CCAGGGTAGC 300
ACAGTGAGGG CTGAGCTCCA GCCAGCAGAT GCAAGACCCA GACCCCAGCC TGCTCTGAGC 360
TGCCATGCCC TCCGGTATCC CGGGGGCCTC CCTGCCCTGG TCCACCCCCA TCACAGCTCA 420
GGGCCAGTCC CCAGGCCCCT GCCCACCCCC AACACCGAGT GAGGGGTGCG CAGGAGGAAT 480
CCATAGTTTA CAGGGAGGGC CCTGCTGGCA GCAGGGTGTG AGGAGCGGGG AGGGGTAGCT 540
GTCTCTGCCT GGACAGGGGC ATGGGCACGG CCAGTCCCAG GCAGGTGGCG GGCTTACCCT 600
TTGCCCACTT TCTTGTCCCC TGGCAGTTCC TGGGGTGTGG GCTCCAAGGA GGCCCAGCAG 660
CCAGACCACC AGCTGCTTCC CCTCCCCACA CAAGCCCTGG CCACAAAGCG CCCTCCCCCA 720
ACTCTGCCCG CCTGTGGTGA CAGCCTCTTG GCACTAGCTC TCTCCTCCCT CCATCTGTCA 780
GGAATCGGTG CAGACAGACT GTGAGAACCA CAGAGGAAGG AGCGATACTG CGTGGACCCT 840
CCCTGCCCCC AGCCTCCCCA GTGTGCTCCC CAGCCCACCC CATCTCTCTC TCCCTACTCC 900
TCTGTCTCTG CCTTCTCTTC CATCTGTCTC CATCTCTCCC TACTGATGAA GACATCGACA 960
GAGTGGGCAT AGGGAGGGGA AGAGGACCAG CCAACCAGTG ACCCCACTCG TAACCACCAC 1020
ACGCCACGGC CACAGCCCAG CCACCCATGT GGCTTCCCTT CTCCCCACCA TTAAGGAGTC 1080
AGATGCTGTG GGACTATGGG CTCAGTGTCC CCATCTGTAC AATGGGTGGA GTCATTCCTG 1140
CTGGCCCACC TCCCAAGGGC CACCATGAGC CTGGAGGCAA CATGTGGGAA GGGCCTTGTC 1200
GACTGCAGAG ACTCATACAA GGCACGTGGC CAGCGCCTCC AGCTTCTTTC TATTCATCAT 1260
GAGAACAACG ATCTCAGTGC TGCCCTCCAC TTGGGAGGAG TGAGGCCAAC ATGGGACACA 1320
GACAGACAGC CACATGCCTG GAAGAATAGA AATGGCGGTG GTAACACAGG CAGGCCCATG 1380
AATGTTATGA TTCTCACCAC AGTCATACGA GGTGAGCAGG GCAGAGATGG GGAAACAGGC 1440
CAGGGAGGGA GGTCACACAG CTGGGCTAGA GGCAGTCTGT AACAGCGGCC AGGCCTCCTG 1500
GCCCTATCCA CACAGCTCCC TACTCAGAAT GTTTGGCCCT GCTCTTCCAG ACCTTCCAAG 1560
ATCCTCTGTT TCTTTCTTGA GTTCTCCCAA AAGGTGAGGA AGAAATCAGT CTTTTCTTTT 1620
GGCAGGCAGG GGTTGAGACA GGGTCTGGCT TCCTTACCCA GGCCAGAGTG 1670
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