| Tag | Content |
|---|
EnhancerAtlas ID | HS052-28476 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr4:48174840-48176030 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr4:48175567-48175578 | CTGAGTCATCC | - | 6.32 | | JUNB | MA0490.1 | chr4:48175567-48175578 | CTGAGTCATCC | - | 6.14 | | NFE2L1 | MA0089.2 | chr4:48175563-48175578 | TGTGCTGAGTCATCC | - | 7.08 | | Nfe2l2 | MA0150.2 | chr4:48175565-48175580 | TGCTGAGTCATCCTA | - | 7.34 |
|
| | 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 |
| GH04I048172 | chr4 | 48174499 | 48176878 |
|
Enhancer Sequence | ATGATTTTCA CATTTATGCA GGCTTGCCCA CACAACCAAC TCTGTACAGA AGGAACTATG 60
CACCGTGAAC TAGTCATTCT GAATTGACAT TGAGATGTCT GGAAAAGACT GCTAGGGCCT 120
TGGACCTTCC AGAAACCTGT GGTGTATTGT AATAACAATT TAATTTATTA TAATAATTTA 180
CTGAGTCCCC ACAATTGGGC TAAGCACTTT ATATGCACTG CCTCATATCA TCCATACAGC 240
AATCCAGTTC TTTCTTAGTG TTAGAATCCT CTTTTTTCAA ATGACAAAAC CAAAGTGGCT 300
GAGGTTAAGT CATATGAGTA GGATATTTAA CCCCCAAATA TCCCTTGACT ATTCCCCTCC 360
TGGAATCTGC CTTTCCAGAC TCCAAGCAGT CTAACTTCCC CACAAAACTC ATCTCGTGTC 420
AGTACCGTGA GCCTGTGAAA CTTCCTTAAA GTTTGTTAGA CTAGCTAACC GCCTCCCCCC 480
ACCAAAAAAA ACCTAATCCA AATTCAGAGT TTCGATAACT AAAACTAGCT TGATATATTA 540
CCTAGCTAAC TTGGGGCATT TGTATTTCTA CGAGAAGTTT CTAGGAATAG CACCCTGTTT 600
TGGCATCTCA GGCTGAAGAG GTATTTGTGG GCCAGTATCT CCCTGAGCAA ACCTCAGATC 660
ACACAATGTT GGCCTCTTGG GGAGAAGGAT CCAGGGAGCT GTGTTTCTCT CTGCCTTAAT 720
TCTTGTGCTG AGTCATCCTA CCACAGCAGA GGCTGTTGGG AGGGAAGAGC TTTGCAAACT 780
TCAAGTGCAG AAACCATTTA AACAAGGAGG GAATACTCTC CCTCAGTAAC ACTACCCACT 840
GGTAGTTACC CACCCTCCTA TTTATATCTT CCATCCACTC ATTCATTTAT TCCATAGACT 900
TAATAGTGTG GTGTAGGAGA AACAGCACAG ACAAAAGGTA GACAGATCTG GGTTTGAAGC 960
CCAGGGAAGA CATGCCAGCT CCTGGGGATC TCCCAGCTGC CATCAGAATG ACTCATCTAG 1020
AAAAGCATGA AGGAGCAACC ATCCCATCTA GGCAGCTGGT GTGGATTCCC CACCATTCTC 1080
TCCATCCGTC CTACTTTCTT CTCCCAGTGT CTTTTGAAAA TGTCTACTTC TACTTTTATT 1140
GTTTTCACTT TGCATCTGAA CCTAATGTAA AATTTCACTA TGAAAATGTG 1190
|
