| Tag | Content |
|---|
EnhancerAtlas ID | HS044-03262 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr12:53336200-53337330 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Stat6 | MA0520.1 | chr12:53337205-53337220 | CTCTTCCTGGGAACT | + | 6.18 | | ZNF263 | MA0528.1 | chr12:53337264-53337285 | TCTTCCTCTTCTTCTTGCCTC | - | 6.11 | | ZNF263 | MA0528.1 | chr12:53337234-53337255 | TTCTCCTCTTTCTCCTCTTCT | - | 6.15 | | ZNF263 | MA0528.1 | chr12:53337231-53337252 | GCCTTCTCCTCTTTCTCCTCT | - | 6.38 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_28333 | chr12:53335699-53336827 | Fetal_Intestine | | SE_28539 | chr12:53335228-53337215 | Fetal_Intestine_Large | | SE_43402 | chr12:53335468-53347645 | MCF-7 | | SE_47355 | chr12:53335691-53342766 | Panc1 | | SE_56972 | chr12:53336031-53342440 | VACO_400 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 53336200 | 53337200 | | chr12 | 53336987 | 53337027 |
|
Enhancer Sequence | AAGATTCTTA ACCCCATGAT TTTCAGTGCC TTCAGCACCC TGAAGTGACA TCACCAGCTG 60
CTCTGACCCC AGATTCTGAT ACTCTCTCTC ACCTTCCCCA TCTCACGCTC CTGTGCTTTC 120
TCTGCAGCTT CCAACTGCCG TGCCACCTCA GTCCCGGGCT TCCTCCTTTT CCACTAAACT 180
CTTCTGTTTG CCTTTGCTTC CCCACCCAAG GCCCAGCCCT TTCAGCCATG TTTTAAGGCT 240
TCTTTGTCCC TGAGCTTCCA CCTCTCCTGC CTTCTCATCC CTCAGTGAAG CCCACCATTT 300
TTTCTCTCCC ACCCCCAGGA TACGCAGTGT TTCTTGTGTG GCTGGTCTCA TCATGAAGCC 360
ATGTTGTGTA ACTGCTGTTG GGATCTCAAG ACCACTGACT CACCTTCTTA TGCCTCATGG 420
TTAGAACACA GAGTTCACCT AATGTGCCAC GGTGTCCTCC TGCCTCTGCC ACACGCTTCT 480
GATTGGGGAG GAAGGAGCCT AGAGAGGTTA CACACAACAC ATCCCAGCTC TGCCACCTAC 540
TAGGATATCA CTTTTCAGGT TGCAGCTTAA ATGTCACTCC ACTCCCCCAG AATCTCAAGC 600
AGGATTAGTG TTTACTGATT TGGGCTTCCA TTGTTCCCTG GACTCACCCA GGCATAGCAC 660
CAACCACACT TTAGTGCTAT TGCTTGTTTA ATTACTGATC AGCTTTACTA AACTGTCTCA 720
TCCTAAGGCA ACCGTCCATC AGTTCTGCGA CCTAACAACC GCTTGGCCTC CCGATTTCTC 780
CTGTCCGTCG CTGATAAACT GCTTGAAAGA AAAGTCTACA TTTTGCCTCC ACTTGGTCCT 840
CTCTCTCCTC CCTCTCAGTC CACACCCCGG CTCCAGGCTC CATCGCTCTA CTGAAAGTGC 900
TCTTTTTGTC CTCAGCCTCC CTGATCCTTT TGTGCACCTG GCCCTGTGGG CCCCCCTTCC 960
TTGAACCTCA TTCTTCTTGG CTTTCATGAC GTCCTCTCTC CTGGTCTCTT CCTGGGAACT 1020
TAGAGATCTA GGCCTTCTCC TCTTTCTCCT CTTCTCCCTC TGTCTCTTCC TCTTCTTCTT 1080
GCCTCAAGTC CCTCTGTGCT GACTCTGCTC CTTCTTTTCC CTGATCCTTT 1130
|
