| Tag | Content |
|---|
EnhancerAtlas ID | HS118-11184 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr20:3960870-3961990 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr20:3961230-3961251 | AAAGCGAAACTGAAAATAAGG | - | 7.05 | | IRF2 | MA0051.1 | chr20:3961228-3961246 | AGAAAGCGAAACTGAAAA | + | 6.32 | | NFAT5 | MA0606.1 | chr20:3961175-3961185 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr20:3961175-3961185 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr20:3961175-3961185 | ATTTTCCATT | + | 6.02 | | RREB1 | MA0073.1 | chr20:3961598-3961618 | TTTGTGTGTGTGTGTTGGGG | - | 6.34 | | RREB1 | MA0073.1 | chr20:3961600-3961620 | TGTGTGTGTGTGTTGGGGGG | - | 6.69 | | ZNF740 | MA0753.2 | chr20:3961612-3961625 | TTGGGGGGGGCAG | - | 6.23 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr20 | 3960925 | 3961306 | | chr20 | 3961377 | 3961729 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH20I003979 | chr20 | 3960553 | 3962264 |
|
Enhancer Sequence | AATGAAAGTG GAACTCGCTA AACTTGCATA GATAAGTAGT CTGCTATGTA CAGTAGTCCC 60
TGCTTATCGA TGGTAGATAT GTTCACAGAC CCCCACTGGA TGCCTGAAAA CCCGGATAGC 120
ACCGAGTCCT ACGTTTTTTT GAACTGATAA CCAAGACCCT AATGGGCAGG TAGTGTACAC 180
AGCATGCAGA CACTGGGCAG GGGATGATTC ACGTCCTGGG TGAGATGCAG TGAGCACGAC 240
AGCTTGAGAT TTCATTACAC TACTCAGAAT GGTGAATAAT CGAAAACTTA CAAATTGTTT 300
TGGGAATTTT CCATTTAATA TTTTCAGACT ACAGTTGACC ATGAGTAACT GAAACTGCAG 360
AAAGCGAAAC TGAAAATAAG GGCGAACTAC TGTAAACTGA TTCAGAGTAT ACAAAAAAAT 420
GATGGAAAGC ATCCCAACTC ATTTAAAGGT GTAAGCATAA TCCTGAAACT AAAACCACAA 480
CTTTACAGCA GAGTTCATAA ACTCAAGGCC TCTGGACTGA ATCTGGCCTG AACAAGTATT 540
TTGTTTGGCC TGTACAAAAT TTTAAAGATT GAGATAATTT AGATTTGGGA GATTTAACAT 600
AAAATTAGCA ATTTCCAGCT CTATACAGAA AAAGGTCAGA TCTAATAACC CTGGGCTCCA 660
TTCTTACACG GCAAAAACAG CCTGGAGCTG AGTGGCCTCT GCTCCCAGGC TGCCATGTTG 720
TTGCACAATT TGTGTGTGTG TGTTGGGGGG GGCAGGGGGA GGGGGCGGCC CTGAATGCTT 780
ATGGGTTACA GTGTAAGTGT GCCTGGCCCT ATTGTCAACA GAATCGCCAT TTGTCACCAT 840
TTCTACCACT CCTTATCACT TCCTAATTCT GGACCAGATG TAGGTTGCCA CTTGTGCTTG 900
GGCTGTTATT TTTCTCAACG TAAATATTTC TACCTCTATC AAAAAAAATA AAAGAAAAGA 960
AATTGATGGT TTCATGATTT TGCCTTCTAC CAAGTGTATT TGGCTGATTC AATTTCCTGC 1020
CTGGCTTCTG TTGGCACTGA GTTTGTGCCC CTGCTTTACG ATTTCTATCT TTGGTTTCCC 1080
CACATCAGAT GACAGAAATA CCCACTTATA TTCTCTTTTA 1120
|
