| Tag | Content |
|---|
EnhancerAtlas ID | HS134-05783 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr10:3132760-3133930 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr10:3133037-3133048 | GGATGACTCAG | + | 6.32 | | JUNB | MA0490.1 | chr10:3133037-3133048 | GGATGACTCAG | + | 6.14 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_02749 | chr10:3132291-3134726 | Astrocytes | | SE_36535 | chr10:3131835-3135114 | HMEC | | SE_38097 | chr10:3131867-3140490 | HUVEC | | SE_45128 | chr10:3132464-3133973 | NHLF | | SE_46169 | chr10:3131883-3140099 | Osteoblasts | | SE_52297 | chr10:3132411-3134292 | Skeletal_Muscle_Myoblast | | SE_64030 | chr10:3132397-3134739 | HSMM | | SE_65141 | chr10:3132488-3134813 | NHEK |
|
| | 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 |
| GH10I003089 | chr10 | 3132041 | 3140100 |
|
Enhancer Sequence | TGGTCTCTGC GTCATACCCA CAGGCTGGGC TTCTCTCTGA GTGTCAGGGC GATGGCATCT 60
GGGGTGGGCA ATTCTTGGTG GGCGGTCCTT TGACTCTCAG GATGCGGAGC AGCACCCCTG 120
TGTCCACCTA CCCCATAGTC ATGACAGTCA AAGATGTCCT TACAGTATCT CCAACATCGG 180
CGAACGTCCT ATGGGGGGAA AATCACTCTT TTGGGGGACC GCTGTTCTAG ACCTATTTGG 240
GCTCAAATTG AGGGGATATT ATGTTTTATT TTTTTAAGGA TGACTCAGTA ATTTATCCAA 300
CAGATTTTTT TCACCTATAC TCTAGTTTCT AACCTAGAGC TCTCTGGGTT ACCAACAGAC 360
CAGGACAGTT AAACAGGTTA CTATTAATTA AAGGGGTTTG TTTTTTCCTT CAGTAGTGCA 420
TGTGTGAAGA AAGTATTAAC CTGGGAACAG TGGCGTTTCT GCTGAAAGCC TGGCCTTCAT 480
CGAGGGACCT CTGCTGTCTG GCCGCTGCTT GAGCTCCTAT AAACCTGGGC CAAGCCTACG 540
TGTGAAGCAT GCCAAGCCTT GGGCTGCATT CCAGGGAGAC TCGGGGAGGG TTTGCCAGTT 600
AACCCATTCC TTTCTACCTG GTGAACCAAT TGTTGCTTCT TTCTTTTTTC TCTTAAGCTA 660
AGGTTTTTCC TTAGAAGCCT ACAAATGGCT TTAGCTTCTT GGAGATGATG ATACTAAGTA 720
TATCAGATGC TTTGACCCAA AGGCCATGCC CAGGGTAAAC TACCCTGGCT CTGGTGGGTC 780
CAAACCAAGC TGGGGCGAGT CAGTTGGTTA ATCCAGGGCT GCCACTGTGT CTGCAGGAAA 840
CAGTCGGCTC CTTGCATTTG GTTTCATTCA TGAATTTCAT ATCCTGTTGT TGAATATTCT 900
TCTGCAGATT TCAGAAATTG TTCATATTAT TATAGCTCTT CAAATATGAC TCACTTAAGA 960
TTCTTGCCGA GCACCGTGGC TCATACTTGT AGTCCCAGTA CTTTGGGAGG CTGAGGCGGA 1020
TGGATCCTTT GAGGTCAGGA GTTAAAGACC AGCGCGGCCA ACATGACGAA ACTCCGTCTC 1080
TACTAAGAAC ACAACAGGTA GCTGGGCGTG GTGTAATCCT TGGAAGGCTG AGGCTTGAAC 1140
TCAGGAGGTG GAGGTTGCAG TGAACCTAGA 1170
|
