| Tag | Content |
|---|
EnhancerAtlas ID | HS007-08941 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr2:46187380-46189010 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr2:46187398-46187409 | GATGAGTCACT | - | 6.02 | | IRF9 | MA0653.1 | chr2:46188858-46188873 | AGTTTCACTTTTGTT | - | 6.15 | | JUND | MA0491.1 | chr2:46187398-46187409 | GATGAGTCACT | - | 6.32 | | RREB1 | MA0073.1 | chr2:46187586-46187606 | GGGCAGGGAGTGGTGTGGGG | - | 6.11 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH02I045961 | chr2 | 46187321 | 46187490 | | GH02I045960 | chr2 | 46187957 | 46193089 |
|
Enhancer Sequence | AATAACTATG TACACCTAGA TGAGTCACTT GGATTTTCTT AGTGCCGGTT TCCTCATTGT 60
GTGGTGGAGG TAGTGATACT AATCGTGTAG AATCCTTTCG AGAAATAGAG AAAATATGTT 120
TTAATCACCT GCTATACCAT AAATCAGTGT TCCCCAACCT TTTGGTACCA GGGACTGGTT 180
TCATGGAAGA CAGTTTTTCC ACTGATGGGC AGGGAGTGGT GTGGGGGGCA GAAGGGGAAG 240
GGCATTAGAT TCTCATAAGA AGCCCCCAAC CTAGATCCCT CACGTGTGCA GTTTACAATA 300
GGGTTCCCGC TCCTATGAGA ATCTAATGCT GCTGCTGGTC TGACAGGAGG TGGAGCTCAG 360
GCAATAATGC TTGCCCACCC ACCAATCACC TCCTGCTGTG CAGCCAGGTT CCTAACAGGC 420
CACAGACCAG TACTGTGGTC CCCTGGGGAT TGGGGGCCCC TGCTGTAAAT GGTGCCTATT 480
ATTTCTAACA TCCCGTTTTC AGTGGATTTT ATCTTTTGCT TTAGAGATGC CAAGCACCCA 540
TCAGCCTTTG ACTGAAAAAT TCCCCAAATT TAGCTCCTGC CTCACTCTCC TTGCAGTTCC 600
TACAATCCTT TCTGCCCCCC AGTTTTCCTA CCTGCCCAGC ACAACCTCTC CAAAAAGGAT 660
CTGAGATTCA CCTATGTTGA ACTTATAATG GCCCTCGCAG AGGCTTTCTG TTTCAACAGG 720
GTTGAAAGCC TGGCACTAAG GAGTAAAGCA AACACAGAGG GGCTGGAAGC AAGAGGGATC 780
ACTTTATTTT TTAGAATACC AGGACTTTAG CGTCTCTGAA TTCCCAGCTC TCAGGAGCTA 840
AGTCAGCCTT ACTCACTTAT ACACAGGCCC TGGTTTCCAT GTGATAGTGA TTCTAATATA 900
AGCTGACCTA TCATAGCATT GATCCTTCCT CTGCTTCTCT CCATAGGCAG GAGTGTGTAA 960
CACCAAGTAC AGTAGTCACA ATACCTACCT CCTTTCCCCC CCCGATTTGG TTGAGCAGTG 1020
AACAAGTCTC AGAGTTAAAA ACATTTTTCC TTGCAATGTT TACCCTGACT TTCTCCTGCT 1080
TTACCTATTA CCTCTTGAAT GAAGTATCTA CTGCTATATA ACAAGTTATC TCAAATTCAG 1140
CAGCTGAAGA TAGTAATCAA GATTTATTGT GTCATTCATT TTCCGTGAGT CGGTTTCTGT 1200
AACCCCATAG CCTTTAGGGC TGCAATGCCT ATGGCACTAA AAGTCTTGTT ATTTGTTTGA 1260
GGGGGGAATG TCCCATTTCA CTTGGCACAT TTCACACCCT TTCCATGTTC ACCAAGTAGC 1320
ACCTGGGGAC AGGCAGAGAC CCCATTTAGA CTTTCAGTTC AGGAGCAGCT TTAGCTGAGG 1380
AGCCAGGCTT GTTAGCATTT CAGAGGTGTA GCAGCCTGCC TTGGCCAGGG CAGTGCTACT 1440
CCATTGCCAG GATTCTTTTT TTTTTTTCTT TGAGACGGAG TTTCACTTTT GTTGTCCGGG 1500
CTGGAGTGCA ATGGTGTGAT CTTGGCTCAC TGCAACCTCT GCCTCCCGGG TTCAAGCGAT 1560
TCTCCTGCCT GAGCTTCCTG AGTAGCTGGG ATTACAGGCA TGTGCCGCGA AGCCCAGCTA 1620
ATTTTGTATT 1630
|
