| Tag | Content |
|---|
EnhancerAtlas ID | HS182-04333 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr11:109946150-109948330 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYB | MA0502.1 | chr11:109946241-109946256 | CTGATTGGCTGGGTT | - | 6.75 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_36695 | chr11:109946953-109950105 | HMEC | | SE_64833 | chr11:109946601-109949861 | 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 |
| GH11I110074 | chr11 | 109945605 | 109950200 |
|
Enhancer Sequence | TTATTATTAC TCAAATCAGT CTCCCCGAGC ACTCAGGGAT CAGAGTTTTT AAAAATAATT 60
TGGCGAGTAT GGGCTCGGAT AGTGAGGAGT GCTGATTGGC TGGGTTGAAG ATGAAATTAT 120
AGGGGGTCGA AGTGAGTTCT TTCTTGCTGA CTTCTGCTCC TGGGTGGGAT TGCAGAACTG 180
GTTGAGCCAG ATTATTTGTA GGTCTGGGTG GTGTCATCAT CTGCTGCATA AGAATGCAGG 240
GTCTGCAAAA TATCTCAAGC ACTGATCTTA GGTTTTACAA CAGCGATGTT ATTCCCAGGA 300
GCAATTTGGG GAAGTTCAGA CTCTTGCAGC CAGAGGCTGT ATGGCATGGC ATAATTTCTA 360
ATTTTGTGGC TAATTTGTTA GTCTTACAAA GGCAGACTGG TCCCCAGGCA AGAAGGGGTT 420
TTTCGGGAAA GGGCTATTAT CAATTTTGTT TCAGAGTTTA AACTATAAAT TCCTTTCCAA 480
GGCTAGTTTG GCCTACGCCC AGGAATGAAC AAGGACAGCT TAGAGGTCAG AAGCAAGATG 540
GAGTCGGTTA AGTCTGATCT CTTACACTGT CATAATTTCC TCAGTTATGA TTTTTACAAA 600
GGTGGTTTCA TTACCAGCTT ATACCATAAA GTCCTGCTGG GAGTCACAGT GGGATACCAT 660
GCAAAATGCT GTGAGAAAAC TTCAGAGAAG CAACTAACCA ATTTTTGGAG TCCAAGAAAG 720
GAAATCCTGC TGGAATTAGG AGACCATAGA CTTTTCGAAG TGTACCCTTT ACCCACTTAC 780
CCACTAAGTG ATCAACCTGT TGCCCAGAGG CGCCCCTTGT CCAGAGACAT CCTGTGCTAA 840
CTTGTTCTTG CATTGCTATA AAGAAATCAC CTCAGACTAG GTGATTTATA AAGAAAACAG 900
GTTTAATTGG CTCAGGCTTC TGCAGGATGT AGAGGAAGGA TGCATCTGCT CAGCTTCTGG 960
GGAGGCCTAA GGGAACTTTT ACTCAAGATA AAGGTGCAGC GGGAGGAGGC ATGTCAAAGG 1020
CAAAGACAGG AGCAAGAGAG AAAGTGGGGG GAGGTGCAAA ACACTTTTAA AGGACCAGAT 1080
CGCTCAAGAA CTCATGCACT ACTGAGAGGA CAGCACCAAG TCATCAGGGA TCCACCCACA 1140
TGACTCAAAC ACCTCCCTCC AGGCCCCACC TCCAACGCTA GGGATTACAT TTTAACAGGA 1200
GATTTGGTGG GGACGCATAT TCAAACTATA TCACACACTT CTGTTACTAT TAAGGACAGA 1260
TTCTGAACAG CAGTGCCTTA GGGTCTTGGA CAACGCTAAC TTCCTTACAG CATTACTCCC 1320
GGAAGGATAT CCAGCCCTTA GAAGCTGATA TAGTTAAAAG CAAATAGATT GTAAAAACCA 1380
TAAAATGCCT GGGGCCATGC TAACTAGAGC TCTGAGGCCT CTGAGAATTG ACTGCAGTAA 1440
ATCTTCCTGT CTTATGCAAC CACATGTCTC TTCTTAGAAG GATCCAGGTT TTTTCAAATC 1500
ACCCGTTAAA ATTATTCATC CATAAATTAT TTTTATTATG ATCTAAAAGG CTTTAATTCT 1560
GTTTGATGTA ATCCGTGCTT TACATACAAA ACATTCTGAG ATAATCTCTA AGTTTTCATC 1620
AATTTATTAG ACATCTACTG AGGTGCCATG ATCATTATCA CAAACTGAAG GGTTTTCATA 1680
TCTTGACTTT TTTAATTCTT TGTCTCCAAT CTTAATTATC ACACACTCAA TTTTCCCACA 1740
CCTGTAGGTT TATTTATATA GTGAAGTAAT TTGGGGAAGG GTATAAATAC ACTGAAGAAT 1800
GCAAAAGTCA ACAGAATCCC TCATCAGACT TTCAAATGGC TTCTGGACAT AGCTCAGCTG 1860
TCTCCTTTCT GGAACTTCCA AACTGTATAG CAGGGGCTCC TTCCTTTATC TGAGCATCAC 1920
ACTAGGGCAT GCTCAGGACA GTTCTCTTTA ATTCATACTT TTTTTTCTTT CCATGTCAAC 1980
TACAGTACTT TGCCCCTGGT ATCACTAACA GAATATAATT CCAGGTGTTG AATTTGAGTT 2040
CATTGGTAAA GGTTAAGGGC TCTGATTGTC TGGAAGAACT CAGTTTGAAT TTTAACTCAG 2100
CCACTGACTA GCTGTGTGAC CTTGGGAAAT TTACGTCACA TCTCTAGACC TAGTTTCCTT 2160
ATCTGAATAG AGTGGTTATA 2180
|
