| Tag | Content |
|---|
EnhancerAtlas ID | HS187-07282 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr14:36157750-36159040 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr14:36158815-36158826 | TCAAGGTCAAT | + | 6.02 | | Esrra | MA0592.2 | chr14:36158814-36158825 | TTCAAGGTCAA | + | 6.14 | | Stat6 | MA0520.1 | chr14:36158712-36158727 | CACTTCCTGAGAAGC | + | 6.84 |
|
| | 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 |
| GH14I035688 | chr14 | 36157554 | 36157828 |
|
Enhancer Sequence | GGGGAAACAT TTGCCTTCGG CTTCGAAAGA GCATGTACAA CAGTTTTATA AACGCCACCC 60
AGGGAGCCCT GCTGTAGTCC TGCCTCATGA CTTGATGACC TAAGAGTACT ACGACTACCT 120
AATTGACTAC TTGCAATTCC TTCTTTTTGT AATATGGTGG TGGGAATCTC TGTGGATTCC 180
TTCACTGTTT TGCTGCTTAC TGATGCAGTA CCAAGTGTAT CTAGAGGTCT GTACACACCA 240
GGTTTTACTA GCTCTGTAGC ACTATTTGTG CTGGTATGGG TGTTGCTAGT GCTGCTATTG 300
CTGCTACCAC TACTAAAGCC ACCGAGCTTC CGCAGTCTCA TCTTCCATGG AGCCTCTTTG 360
TTTTCCAGAG GATTATAAAA CTGAACGGAC TCAGTGGATG GCCTAAAAGT AACATGAACA 420
CTATTTCGTT TTTTAGTAGC AATTTTCATG ATTTTGGCTC TATGAGTTAC TGTTTCAGAC 480
AAGCTCCTTT TAGTTGGAGA AAGTTTGCTA GTACTTGTAA CATGAGGCAT TCTGCGGTTA 540
ACAGGTGCTT TTAGTGTTGC TTTCTTGGCA CGCATAACAT GTGGGACAGT GATTTTTTCA 600
TTAATTTGCA CACTCTTAAG CTTTTCAACT AGTGTTACAT CAACACAAGC ATCTAATTCT 660
GTGGCTGCTT GTCTGTACAG ATGTTTCCTT TTTTCTTTAT CACAAGGGCT ATCTAAACTA 720
GGCTCTGATG GCTGTTTATC AGTGTTTAGT TGCTTAGATT TTTCAGAAGT TTGTGTTCTA 780
AAAAAACTGT CTGACTGGTT AGGTGCGATA TTACTCATGA AGACAGCTGA GTTTGGTTCT 840
TTCTGAAACT GTAGGTTTTC AGGAGTCCCA ACAAAAGAGG TGATATTTTC TGATTCAGTT 900
TCCTGATCTG TGCATTCTAA TTTATCTAAG GATAATCTTT CACCCCTATT TACTGCAATA 960
GTCACTTCCT GAGAAGCTGG GTCTTTCCCT GTCTCATTTT TACTATGATT TTCCTGGTTT 1020
TCCTTAAAAT ATTCTTTCAG GGTGGAAAGA AGATCATCAT CTCCTTCAAG GTCAATGTAC 1080
TGGATTTGTT CAAAAGCTGA ATCTGCAAGT TCTACTGGAC CTATTAAATG ACAAAGATGG 1140
TCATATATGC TATCACCAAC TTCCAGAGAA GACTCTCTAC TATGAGTATC AGTGATGTGG 1200
CTTTCAGTGG ATCTAGTTAT TGAAGAAGCC TCTGTGGAAC TCTGCAAGCT TGGTGCATGA 1260
CGGGATGAAC TGTCAATGAC AGGAACTGCA 1290
|
