| Tag | Content |
|---|
EnhancerAtlas ID | HS176-19148 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr19:45378680-45379960 |
SNPs | | Number: 3 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HEY2 | MA0649.1 | chr19:45379732-45379742 | GACACGTGCC | + | 6.02 | | Npas2 | MA0626.1 | chr19:45379732-45379742 | GACACGTGCC | - | 6.02 | | Zfx | MA0146.2 | chr19:45378766-45378780 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_28236 | chr19:45378736-45379672 | Fetal_Intestine | | SE_29374 | chr19:45378802-45379490 | Fetal_Intestine_Large |
|
| | 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 |
| GH19I044875 | chr19 | 45378835 | 45381033 |
|
Enhancer Sequence | CCCGGCTAAG TTTTGTATTT TTAGTAGAGA CAGGGTTTCA CCATATTGGT CAGGCTGGTC 60
TCGAACTGCT GACCTCAGGT GATCCACCCG CCTCGGCCTC ACGAAGTGCT GGGATTATAT 120
GCATGAGCCA CTGCGCCTGG CCAGAAAAAG ACATTCTTAG AAACACGCCA GGGCGACGGT 180
CCATGCAGCA CACCTGTGCA AACACGCAAT GTGCAGGCCC CCCAGAAACA TGACTGAAGG 240
TGTAGGGACA AACTCCCAGA CAGGGGCTGT CCCTGTCATG CAGACAGACT AGCCACGGAG 300
GGACAGAAGC AGACCCCCTT ACTGAGTCAT AATCTTAGAA TGCACACACA CTTGCAGGGA 360
CACCCGAGGG AAAACAGACA CCTCTTCAGG AATCCAGATA CAGCCAGGGA GATAGGACAC 420
CCCTACGGGA AACACTGTCA CAGACAGCAA ACCCAGAGAG ACAGCTGTCC CGCTCTGGGC 480
TCGCCTGGCG CGTGAGGATG CACATAAGTC CCCGGAGGAA GACGTCACAC AGACACGCTG 540
GGGGCAAAAC TAATCCAGGA CAGCAACGGC TGCACACGGA GGAATGTCAT CCCTCACTCA 600
CAGACCCTCA GACGGAAAAT CAAAGACATC CTGGGAGGAG CTTCTTCCCA GGAACCCTCC 660
CGAAACTCCC CGAAACTCCT CCGAAATTAT CCAGAAAGTC CGTTAGGGAG ATTCTCATTC 720
AACAAATATG TGTTTCCTGT TTGCTAGGCA CTCTTGCTGA GGTTGGGAAT ACAATGGTGA 780
ATGAGCCACA GTCCCTGCCC TCAGTAGCAC ACCCAGGGGA GGGTCAGCTC CACCCGCCCA 840
GACAGACACC GAACTGGAAA TACACCCCTA ACCTCTACCC CAGATACACC TGACAAGCTG 900
ATCCCCTGCC CACACACCCA GCAGGTGGCT CCAAGGTCAG AGCCTGCAGA ACACAGACGC 960
AATAGAGAAA GACTCAGCGC TGTGGAAAGA CACCCCCACC TACCCACGAC AGTGGCCACA 1020
GGGCCACCCC CAGCCAATAA CACCATTACA AAGACACGTG CCTTCAGATA ATGCCTGCAG 1080
AAACGTGCAT GCTCCAAGCA CTCTAGAAAT CCCGTCTCAA GCAGTGAGTG CCCCGACAGC 1140
CACAGCCAGA GGAGACACAC TCAAAGCTCC TGGGGTCACT CTCAGAGGGT CTCTGAGCCA 1200
CGAACCCACA TCCAGGCACA CACAGAGTCG TCACAGAGAC ACAGTATGGA GTCCACAGCA 1260
GCACGAACAT AGGATACGAA 1280
|
