| Tag | Content |
|---|
EnhancerAtlas ID | HS187-15021 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr20:3960820-3961990 |
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 | CTTGAAAATA TAGAAATATC TTCACAAAAA AGGCTTCAGA CCCCAATGGC AATGAAAGTG 60
GAACTCGCTA AACTTGCATA GATAAGTAGT CTGCTATGTA CAGTAGTCCC TGCTTATCGA 120
TGGTAGATAT GTTCACAGAC CCCCACTGGA TGCCTGAAAA CCCGGATAGC ACCGAGTCCT 180
ACGTTTTTTT GAACTGATAA CCAAGACCCT AATGGGCAGG TAGTGTACAC AGCATGCAGA 240
CACTGGGCAG GGGATGATTC ACGTCCTGGG TGAGATGCAG TGAGCACGAC AGCTTGAGAT 300
TTCATTACAC TACTCAGAAT GGTGAATAAT CGAAAACTTA CAAATTGTTT TGGGAATTTT 360
CCATTTAATA TTTTCAGACT ACAGTTGACC ATGAGTAACT GAAACTGCAG AAAGCGAAAC 420
TGAAAATAAG GGCGAACTAC TGTAAACTGA TTCAGAGTAT ACAAAAAAAT GATGGAAAGC 480
ATCCCAACTC ATTTAAAGGT GTAAGCATAA TCCTGAAACT AAAACCACAA CTTTACAGCA 540
GAGTTCATAA ACTCAAGGCC TCTGGACTGA ATCTGGCCTG AACAAGTATT TTGTTTGGCC 600
TGTACAAAAT TTTAAAGATT GAGATAATTT AGATTTGGGA GATTTAACAT AAAATTAGCA 660
ATTTCCAGCT CTATACAGAA AAAGGTCAGA TCTAATAACC CTGGGCTCCA TTCTTACACG 720
GCAAAAACAG CCTGGAGCTG AGTGGCCTCT GCTCCCAGGC TGCCATGTTG TTGCACAATT 780
TGTGTGTGTG TGTTGGGGGG GGCAGGGGGA GGGGGCGGCC CTGAATGCTT ATGGGTTACA 840
GTGTAAGTGT GCCTGGCCCT ATTGTCAACA GAATCGCCAT TTGTCACCAT TTCTACCACT 900
CCTTATCACT TCCTAATTCT GGACCAGATG TAGGTTGCCA CTTGTGCTTG GGCTGTTATT 960
TTTCTCAACG TAAATATTTC TACCTCTATC AAAAAAAATA AAAGAAAAGA AATTGATGGT 1020
TTCATGATTT TGCCTTCTAC CAAGTGTATT TGGCTGATTC AATTTCCTGC CTGGCTTCTG 1080
TTGGCACTGA GTTTGTGCCC CTGCTTTACG ATTTCTATCT TTGGTTTCCC CACATCAGAT 1140
GACAGAAATA CCCACTTATA TTCTCTTTTA 1170
|
