| Tag | Content |
|---|
EnhancerAtlas ID | HS091-25366 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr2:25351200-25352840 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr2:25352212-25352223 | GGGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr2:25352213-25352223 | GGGGCGGGGC | - | 6.02 | | RREB1 | MA0073.1 | chr2:25352214-25352234 | GGGCGGGGCGTGGGGTGGGG | - | 6.03 | | RREB1 | MA0073.1 | chr2:25352226-25352246 | GGGTGGGGCGTGGGGTGGGG | - | 6.62 | | RREB1 | MA0073.1 | chr2:25352231-25352251 | GGGCGTGGGGTGGGGTGGGG | - | 6.86 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr2 | 25352140 | 25352468 | | chr2 | 25351723 | 25351811 | | chr2 | 25351877 | 25352613 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I025128 | chr2 | 25351786 | 25352750 |
|
Enhancer Sequence | GGTAAGCAGG CCGGGATGGG GCAGGACAGT AGATATAATC AACCCTCCAA GGGCTGCTTG 60
GGAACCACAT GGTTTGGGTT GGTCAGTAAA ACTCAGCTAC AAGGCCAGGG ACATGGCTTT 120
GTGGCTTGTT CTGCAGTGAG TCCAAAGCTG GCTCCCTAGA AGCCATGGGT CTGACTTTGT 180
GCCAGCCCAC AGTGTCCCTT AACATGTGCG TTACCGAAGG AGGACAGTGT TGGTGCTGGG 240
CTCCCTGGTG GGTAAATCTG TTGGTAATAA CACACAGAAC CAAGAGTCTG GTTACCTTTG 300
TCTCCCTGGA AGCAGGGCCA AGGAGGCTTT AAGATGCCTT TTGTGGGCCG GGCGCGGTGG 360
CTCACGCCTG TAATCCCAGC ACTTTGGGAG GCTGAGGCGG GCAGATCACG AGGTCAGGAG 420
ATCGAGACCA TCCTGGCTAA CACGATGAAA CCGCGTCTCT ACTAAAAAAA AATGCAAAAA 480
AATTAGCTGA GCGTGGTGGC GGGCGCCTGT AGTCCCAGCT ACTCGGGAGG CTGAGGCAGG 540
AGAACGGGAG CCCGGGAGGC AGAACTTGCA GTGAGCCGAG ATCGCGCCGC TGCACTTACA 600
GCCTGGGCGA CGGAGCGAGA CTCCGTCTCA AAAAAAAAAA AAAAAAAAAA AAAAAAAAAA 660
AAAAAAAAAA GATGCCTTTC ATGGCTCCGA TCACTGCGGA CTTTCCATCT GGACCTTCCT 720
TCCTCTGTTG CTTCCTGATG CTATTTCAGG CCCTGAAAAC GTGCATGCTT GACCAGCCCG 780
CAGCCACTCA GTAAGAGCTT GCAGATACTG GGTTTTAATC CTGGATCCCC TAAGCATGGG 840
ATTCATTCCT GTCCCTGCAC CCTCATTTTT CCCCTCGGTG AAATGGAATG GGGAGAAAGG 900
CCCACGTTGC TGTCCCACCT GGGCTATCTG TGCACTAGGC TAGTTAGGTC GGTTGATCCC 960
AGGCTACTAG AGCTAGACTC GGGTCGACGG GGGCGGGGGC GGGGGCGGGG GCGGGGGCGG 1020
GGCGTGGGGT GGGGCGTGGG GTGGGGTGGG GTTCGTATGC CATCTGGTGG CTGTTTCTGG 1080
AATAGCATCT CACTGACAAG CTGCTGTGGT CTCTGGGCTG GGAGTCCTCC GGCTCCTGTT 1140
CTGTCCAGAT GTGGGCCCAC TCCCTGTGAC TTGAGTATCA TTGACTCTTG CCTGAGCCAA 1200
CCACTGTGCC TTTCCTTTTC CCTCCCTCTC TTTCCTCTCC TTTCTTCCAC TTCTGTTTTG 1260
TTTTTTGCCT CCCTTTCCTA TCTTCATCTC CCATCTCCTT TTCCTTCTGA AGTCTTAGGT 1320
GCATCAAGAC ACACATGTTC TACACCTCAC CTGGCCCATG GGGCTCAGAG CATCCTTCCC 1380
ACAGTGGTAC ATCTGGAAAT CTTTAAGGAT TTCCAGAAAA AGAACTTTAT CTTTTCTTCT 1440
CCGGTCTTCC CCCACTTCCC CCAGTGGGGG CTTCTTTACC CCCATTTAAT TTCTGACAGC 1500
TGTGACGCCT CCCCTATTGC CTAGTGCAAC CCATGTCAAA TTCCTGCTTG TCTTGTGTGG 1560
ATGAAACACG GAAAGCCGGG ATTGTACAGA GCCTGACCCC AGCCTGCATG CCACCCTCTA 1620
CCCATGTGCC TCTGTCTCCC 1640
|
