| Tag | Content |
|---|
EnhancerAtlas ID | HS043-09808 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr12:26392410-26393840 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| LMX1B | MA0703.2 | chr12:26393315-26393326 | GATTTAATTAA | + | 6.02 | | RARA(var.2) | MA0730.1 | chr12:26392894-26392911 | AGTTCATCTATAGGTCA | + | 6.14 | | TFAP4 | MA0691.1 | chr12:26393015-26393025 | AACAGCTGAT | + | 6.02 | | ZNF263 | MA0528.1 | chr12:26393459-26393480 | AGAGGAGCAGGAGAAAGAGAG | + | 6.79 | | ZNF263 | MA0528.1 | chr12:26393462-26393483 | GGAGCAGGAGAAAGAGAGGGG | + | 7.22 |
|
| | 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 |
| GH12I026238 | chr12 | 26391098 | 26393585 |
|
Enhancer Sequence | CAGAATGTGT TTTTCCCCTA GAGTCCTTGA GCACAGACCT GCGGTTTTCT CTCTCCTGGT 60
TTTACAGTCT ATCTGCCTCA AGCCAAGAGA CTTGGCTCTG CTCCCCCCTG ACTCAGAGTC 120
TCGGCTGGTA GCTGAACCCA GGAAGCCCTG GCCCCACGTC TCTCCCTGGA ACCACCAGAC 180
CACACAGCCT CCTGTGCTCA ACCCTTTGGC TGGGTGTCCT GCCTCCTCTT TGTTTGGAAA 240
GAGATGTCTT ACGTAACTCC ACAACCTTCT AAAGGCTCCA TTGTCTTCCA CTTGGGAGAG 300
CTCAAAACAA CCCATTAGTG ACTTATGACT TATCACAAAG AGAATCTATT GCCCACATAT 360
CCACAGCCCC CATGGAGCTA GCCTCACCTA TCTTACTTAG ATCAATAATC AACAATGAGA 420
CTTAATGACT TGTGGTCTTT GGGAAATTAT AAGTTCAGTA CAAGGTGCAG GAAATACAAA 480
GGCTAGTTCA TCTATAGGTC ACGGTACTTC GCCCAGGCAG CACATGAAAG TCATTTGTAA 540
TTCAAGATTG AGACAGGCAT AAACAATTCT GATCTGATTA TTCTTTTACT AATCTGATTT 600
TGATAAACAG CTGATGAAAA TGGAAGGTGT CTGGTCATCA GAGGAGAGAT ACTCAGGCAG 660
TGAAATAAGT TTTCCTTATC TCACTGGATA GGGATTTATT TCAAGGCTCC TATTAATAGC 720
CCCTAATGCC AAGAACTGTG ATCGCTGCCC TGGACTGCAA GAGCCTTCTG AGCAAAATGA 780
CAGAAACCCA TTGGGTAGGG CATTCTCCTT CATTTTTATT TTCTATAAGT CTCTGATTAG 840
CCCTGTTGGG AATTCTAGTA ATTATTTTAA GCTGGCACCT TTAGGAAAAA AAATATATCT 900
CTTAGGATTT AATTAAAAAT GAAAAGAACC TCTGCATGAT GTTGCCAAGG AGCTTTCACT 960
GTTTAAGGTG GGGTGTAGAC CAGGAAGAAT AAAACACTCT GCACTAGGTG ACATTTCCAT 1020
CTGGTTCTGC TGCCAGAGCA GCCCTGGGGA GAGGAGCAGG AGAAAGAGAG GGGACAGCCT 1080
GCTCCAGCCT GCTCTCTCCT CCCCATGGAC CTCATGGTCT TTCAAGGATC CTGCAAGTCC 1140
TTTGCTTCTT TCTTTCTGCA GCAGACATTT TCTCATCTGG GACCAGCTAT GTGACTTGTT 1200
TCAGGTGGAG GCACATTTCT TTCCCTGCTC AGTGACATGT GAGTCCTCGA CAAGCTTTCA 1260
GAAGGGATTC CTGAACTTGG TGAGGCACAG CCCTCTCCAA CTGCCTTGTG GAGCATCCCT 1320
GGGCAGCATG CAGAGGAGAG GTGAGAGGCT GCCTACCCGT GCTGTGGCTG TCCCTCCCAC 1380
CTCCCTTAAA GCCTCCACGT CAGGCGCCAG TCCACCAGGT TCACTGCGTG 1430
|
