| Tag | Content |
|---|
EnhancerAtlas ID | HS148-04366 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr12:76152890-76154120 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr12:76152937-76152958 | GTTCACTTTCACTTTTCTAAC | + | 6.16 | | IRF2 | MA0051.1 | chr12:76152936-76152954 | TGTTCACTTTCACTTTTC | - | 6.42 | | PRDM1 | MA0508.2 | chr12:76152939-76152949 | TCACTTTCAC | + | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_34233 | chr12:76152506-76156922 | HCT-116 | | SE_47361 | chr12:76153166-76156726 | Panc1 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 76152920 | 76153104 | | chr12 | 76153125 | 76153270 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I075758 | chr12 | 76152704 | 76155195 |
|
Enhancer Sequence | TACCTTCTTT CCAACCTCTG ATCAATGGTC TTATTTCCCA GCTCACTGTT CACTTTCACT 60
TTTCTAACTT AGTATTGAGC TGGGCTGACC ATCAATTTTC TGACATCTTT CATGTAGCTC 120
TGCATCAGCT CTCTTGTTCC CCAAGGACAG CCCTAATGTG CATGGCCTTT CAGGGATTTA 180
GTGGCGCAAA GATGCTCTAA GTTTTAATTC TATGATGGGG GTTAATTATA GTTCCCTTTG 240
TTTCCATTAG AGGGATTGGT ATATTGCACA GAGCTACAGC TAGATTAGTT TTACCTTAGC 300
GTAGTGTAGT GGTTTAAAGC TTGGACTTAG ATTCAAGTAG ACATGAGTTT GAGTCCTGGT 360
ACTACCGCTT AATTGTTACA TGACCTTAAG CAAGTTATTT TTTTTAACTT AGTTCCTCTT 420
CTGAAAAATA TAAACTAATA CCCGCCTTAA AACTTTTACT GATCAAATGA GATGATCCAT 480
GTAAAACTCT TCATGCCTAG CATTTAAAAA GTATTCCATC AGTGTTCTCA TTATCATTAT 540
CTACTTGTAC GGCATCATCC CTTCACCACT TCTCACTTCA AATGTAATAT TCTAATAGAA 600
AGTACAACAA CCAATCATTT TACATTAATT ATATTGCAGT TCTTTGTCTT TTTTGTCCCC 660
TGCCAAGCCA ACAATTTTAC CTAAGAATGT TCTTCAAGAA ACACTGCTCT TAATTCTTCC 720
ATGCAATAGA TTCCTTTAAG CAAGTATAGG ATTCAACAGA GTCCTAAAAA GAGGTTAGGA 780
ATATGCATTG AGTCATGTCC CTGTAGAGCT GGAAAGCGGA GCAACCAGTG CTGAAAGAGA 840
GTGCAAAAGC TGCCTTAAGA ATTTGGAGCC AGAGTCTTTG AGAACTTCTC AAGCATAGGA 900
ATCAAAGAAA AAGACCATGG AAACCTTCAA AGTCACATGT GGGATACTAG GAGTATGAAT 960
CATAAAAAGT AAAAATAGTG CCTTTGGTTT GCCCTAGCTT GATGACTTTG CTTTAGCTCA 1020
CTAGCTGACT CAATGAAAAC CATCAGTCAA TTCTGTTGTT TTGCATTTTG AGAATATGAT 1080
AATTGACTGA CTGTTTCACT TTGGCCATCT TGTGAGTAAG CAGTATACCC CACCTTGATT 1140
ATCACAGAGT AGCTGCCTGA ATTACATGGT AAAAATATGC ACATTCACCT TCAATGTCTT 1200
AGCTGGAAAT GCCTCCTCTT TGTGTCCTAG 1230
|
