| Tag | Content |
|---|
EnhancerAtlas ID | HS047-31690 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr7:133838980-133840370 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr7:133840219-133840240 | GGATTGAAACTGAAACCATTG | - | 6.02 | | IRF8 | MA0652.1 | chr7:133840222-133840236 | TTGAAACTGAAACC | + | 6.5 | | IRF9 | MA0653.1 | chr7:133840221-133840236 | ATTGAAACTGAAACC | + | 6.73 | | NFAT5 | MA0606.1 | chr7:133840342-133840352 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr7:133840342-133840352 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr7:133840342-133840352 | ATTTTCCATT | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GAGGATTAAC CCAGTAAGCT AATTCATTGT AATGTGTAGT GATTTATCAG ATTATGTTTC 60
TTCTTATCAG GAAGTCCCGA GACCTGTGAA AGAACACGAA TAATGTTAGG AGGAAGGGCA 120
AGTAACATTT TGTGAAGGTC CTTAAGAGAA TGAGAGATTG GGGAGATAAA GATATTGAAG 180
ACCATCTATG AACTCAAAGC TCTCTATGGC CCAGGCCTGC ATATTGACTG TTGGCAGTGC 240
CACCAGGCCC ACATGAGGTG ACTGTGGGAG CAAGTAGAGG AAAAAGCTGT TGTATCACTG 300
TAGAAAGTTC TCTTTACTCA GGAGCCTGAT TAATTTAGAG TGTCTGAAAT TCCTTGATAT 360
TTGAAGGAGA GTGAAAAGCT GAGAAACAGG AGGAAATAAT TTTTCTGGAA TGAGCATATT 420
TCTCAACAGA GATGTTCAGG CAACTCCTGC TCCTTTGCCC TAGTGGTGTT AGTAACCGCA 480
ATGGTACCTG CAGAAACCAT AGGTATGATT GCAGTGAGCA TCTGAATTCC TCCTCCTTTC 540
TGTCCTTGCA GTGCTGATTT CAGAACACGT GACTAGCTGT GGGATTCCAA GCTAGAGAGT 600
AAGATGGATG TGCCAAGGGA ACTGTGGTTA GCCTCTAATG TCTTAGAAAA TTACTGTAGA 660
CACAATAAAC AAGCTTTCCT TTTTGATTCC TGATATCTCT TGATAATTTC AGGATTCCTG 720
TTTTCTAGTT TTCTGATCCT TGCCTGCTTC CCATGAGAAT ACTTCCTGAG GCAGATACCC 780
ACAAGCAGTG GTTTTATTCT GCCATGATTC AGAGTATCTT CATCTTGGTT GGGGTAGAGC 840
TACCAGGACA CTTTAGTACT CCTAAAATAG GACTTAAACA TGATTTCTGT CTCTGCTAAA 900
CTGAGACAGA TGGCCATTCG AAGTTTTCCT TGCATAGTTT TTGTTGCCAA AGATTGCCTG 960
CTCCAAGGGT ATTTTATTTC ATCCATACCT GAGTGAGATA GTTTAATCTC CTATTTCTTA 1020
TGTTTCATAT TCATATTTTG TTACAATCCG TATCTACAAA GATCTGGTCT TTGTTCTAGT 1080
TCCAGAACAA TTATTTAAGC AGCCCAAAGA AAGTAGAACC AGAAAGGATA GTATTAGTGA 1140
GCATAAACAT CTGTTTGTAG GGCTATTCTG GCAGGAAGCT TTATGAAAAC AGATTTGAAA 1200
ATGCATATTG ACCACAAACA GAGCTATACT TCAGTCTAAG GATTGAAACT GAAACCATTG 1260
AGGAAAACCC AAGAATTTCT GGTACATTTT ACATTTTTGT CTAGTTTCCT TATTTACCTC 1320
TTTCTCTGGC GTAGGTATTT TCAGGCTTAA TCCCAGCCTT GAATTTTCCA TTTCTGTGCT 1380
ATTGACCAAG 1390
|
