| Tag | Content |
|---|
EnhancerAtlas ID | HS044-04084 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr14:23493780-23495050 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PBX1 | MA0070.1 | chr14:23494126-23494138 | TCATCAATCAAT | + | 6.44 | | ZNF263 | MA0528.1 | chr14:23494875-23494896 | CTCCCTGCCTCTCTCTCCTTC | - | 6 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_33418 | chr14:23489747-23495941 | H2171 |
|
| | 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 |
| GH14I023024 | chr14 | 23494036 | 23495490 |
|
Enhancer Sequence | TTTCGTATTT TTAGTAGAGA CAGGTTTCAC CATGTTGGCC AGACTGGTCT CAAACTCCTG 60
GCATCAAGTG ATCTGCCTGC CTCCGTCTCC CAAAGTGCTG GTGCTGGGAT TACAAGCCTG 120
AGCCACTGTG CCCCGCCCAG CTCCTGCCTA TTTCAACCAT GTAGTCTGAG TCCACACCAG 180
CAGCTCCCTG ACTGCAGGGG CTCCTGAGAT ACTTTCCTGC AAAAAATTTC CTTAGGCACG 240
AGTCATTTGT TTTCCAAACC CCCTTCTCCG ATTTCACTAA TTCCCAATTT CCCTGCATTT 300
GACAAATGCA ATTAACAAGC CTCGATCAGT TCCTGGCCGA CAGCCCTCAT CAATCAATAC 360
GAAGACTGCA CAAGGCTGAG GGGGAAGGGA AGGTAGCTGC AGTACAGGAG AGGAGGGTTT 420
ACCCCCTCTT CTTCTGTGAA TGACTTCTCC AAACCTCTCA GTCTCAAAAC ATGACACTGG 480
GTTGTCACCT TCACCAACCA CTTTCTGCCT TCTGACTAAA TACAAGGTGG TATTGTTTGT 540
GTCCTCCGCT CCCATTTTTT AAAGGTTTCT CCCATCAACC TCCTCTATCC CCTGTCTTCT 600
CTTTAACAGA AGGCCTTGCC ATCTGCTGCC ACCATAGCTT GGGAACTCCC CCCAGCCCCA 660
ACAGTGCTGG GTGTGATAAA TCAGCCATCT CTCTGCTCTC AGCAGGGCCT CTTCCCCACC 720
CACACATTCC AGTGACAATT TAGTGCTGCT TCCTGACCAG GAGGCTATAA AATCACCATC 780
ACTACCCTCT CCCCTCCACA CATATGCACT GGAGGACCAA AAGGACAAGG GTCACCAAGC 840
TTGTGGTTAC TACTGCTTTC ACAGCCACTT CTTTGTCCTC CCCTTCCCAG GGTCCAAGCC 900
TTCCCTTCCC AGTTGGTTTA AGAGTCAAGA TTTACCCTCT TCACCCTTCC GCTCTGCATG 960
TAGCCTCAGC CTCCCTTCCC CCACCACAGG GTGACAGCCT TTTCCGCTGG AGCCCTGCCT 1020
GGTACAGCCC TGTGCATCTT TCCACCTCAT CAACTTTTCA TCTCTTTGTA AACCAAATCG 1080
AGAAGTGTCT CCCTCCTCCC TGCCTCTCTC TCCTTCTCCG TTATTAGCTT CATGAGTGGG 1140
GACATTAATG TATTCACTAG ACAATGTCTT CACACCACTG TTTCCTGTAA TTACAGTCAC 1200
TTCCCTTCCA CTGTCCTGGC TTATTTGACT GAAAAGTGCT TGGAGGAGGG ACAGTGTGGA 1260
CAAAAGATGC 1270
|
