| Tag | Content |
|---|
EnhancerAtlas ID | HS145-17893 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr3:124857940-124859660 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Ar | MA0007.3 | chr3:124859385-124859402 | TGGAACACCATGTGCCT | + | 6.07 | | Ar | MA0007.3 | chr3:124859385-124859402 | TGGAACACCATGTGCCT | - | 6.7 | | NR3C1 | MA0113.3 | chr3:124859385-124859402 | TGGAACACCATGTGCCT | - | 6.05 | | Nkx2-5(var.2) | MA0503.1 | chr3:124858009-124858020 | CTTGAGTGGCT | - | 6.62 | | RARA(var.2) | MA0730.1 | chr3:124859003-124859020 | AGGTCACTCCAAGGACA | + | 6.17 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_27311 | chr3:124858008-124861858 | Esophagus | | SE_32613 | chr3:124857437-124858831 | GM12878 | | SE_32613 | chr3:124858836-124862530 | GM12878 | | SE_46094 | chr3:124857933-124861421 | Osteoblasts |
|
| | 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 |
| GH03I125139 | chr3 | 124857957 | 124863844 |
|
Enhancer Sequence | TTCTCGTCAG CTTTTCTATG TATGAAGAGC TTTTCTTTCT TTCCGTTTGT ACTCTGTTTC 60
CCAAAATGAC TTGAGTGGCT TATGAGAAAA ACATAAACAA GACAGGAAAA ATAAAATAAG 120
GACCAAAGAA AGAAAGAAAC TGAGCAAAAG AGAGAGAGGG TGAGAACACC CCCAGTCGTA 180
CCTCCATGAC CCACAGTCTG AGGCCTTATT CAGAGAGAAT TTTCTAACTC TTTGACCAAG 240
CGCACTGAGG CAGGGCATTG GATCTGGTGG CCCATCCCTC ACATGGGCCA CTTTCCAGTG 300
GACAACAAGG AGCCCCCAAA GCTGGCACAG TGGACCCTGC CTCATTTCCT CTGCCCCTAT 360
TTTCCCAGGC CCTCATGACT TGCACCCCTC ACCTATCACC ACCCCACCTC ACGGTCCCCT 420
GTCCTGAGCC AGTCCCCAAA GAGTCTTGCT CACTGGTCCC CATCCTGCCT GCTGGGGCCT 480
GGGTCTCTTT CCCACACCCT GAACCTGGTG GCCCACCCAG ACCTCAGGCA TGGTTGACTC 540
TCTGTTGGGC TTATGCAGAG TGGGTGCCCA GGGGAGGCAC TCATGTCTCT GACTGGCCGG 600
TACTGGCTAG CTAAGCATGG TGTGAGGTCA GTGGGTCACA CCCAGGGTAG GGCTGAGGTC 660
CATGCCGCCT GCCATGCCCT CCGACAGTGG CTCTTAATGC CTGACTTGCT GATGCCCAGA 720
ACAAAGGTTC CTAATTCTTT TAGTTGCCCC CATTTGAGAG TCTGATGAAT ACCATGGTCC 780
CTGTCCCCAT AGACACCACA TTTTGCATAC CATTTTGGGG AAGGGCAGAT TTCTGAAGCC 840
TCTCTGGAGA GCATGGACCT TAAGGTTCGA GACCTCTACT CTAGCAGCTA CATCTGCACG 900
TGAGATTGTC CCGCCAGGAG GCACCTACAA CTTCCCAAGG CCTGACTGCC ACCATGCCCT 960
GCCTCAGAGT GGACAGCAGC CCTGAGAGTG ACATAGCCAA TAATGTCTTC ATGCCACAGT 1020
CCTTGCCAAG CAATGGCCAA GACTGTGTGC ACAGAGATTG TGCAGGTCAC TCCAAGGACA 1080
CCACAGGGCA ACCTCACTTC TGAAAATAAT GCTGAGCGAC CAGTGACTGA ACCCTTCCTA 1140
CGTGCCAGCC ACTGAACAAC AAGACCTTAC AATGTCATAC TTGTACGATG ACTAACTGAG 1200
GACACTGAGG CTCCGGAACG TGAAAAAGCT TGTCCGAGGG TTACATAGCC AGATCTGCCT 1260
GTATTTCACC CACTGCCTCT CCCGGTGGCA GAAGCCAGGC CTCTCTCCAG GAGGTGGGTT 1320
CCCAGGCCCT GGCACTGCAC CCCCTTACAG CACAGGTTGC CTTTCAGCCC CAGGAAACAT 1380
GCCCACAGAG ATCATGGCAT CTCCCCCGGC CCCATTTGTG TAGGGCAGAC AGGAGTCCTA 1440
TCCTGTGGAA CACCATGTGC CTACCGGTAT GCAACTGGCT GGAGCTTACA CAGCTGGGAG 1500
GACACAGCCT GTCCTGGACC CCACATCTGA GTGAATTCAG GCCTCCATCT ACCACACTGA 1560
CCCTCTGTAA TCCATCCCAA AGTCATTCCC CAGGAATTTC CTTTTTTTTT TTCTTTTCTT 1620
TCTTTCCTTT TTTTTCTTAA AGAGGCAGGG TCTCGCTCTA TCACCGAGGC TGGAGTGCAG 1680
TGGCACTATC GTAGCTCACT GCAACCTCAA ACTCCCAGCC 1720
|
