| Tag | Content |
|---|
EnhancerAtlas ID | HS151-00135 |
Organism | Homo sapiens |
Tissue/cell | OCI-LY1 |
Coordinate | chr1:16275320-16277690 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MITF | MA0620.2 | chr1:16276939-16276957 | AAAGGTCACGTGAGCACA | + | 6.13 | | MITF | MA0620.2 | chr1:16276939-16276957 | AAAGGTCACGTGAGCACA | - | 6.13 | | MSC | MA0665.1 | chr1:16276484-16276494 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr1:16276484-16276494 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr1:16276484-16276494 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr1:16276484-16276494 | AACAGCTGTT | - | 6.02 | | RREB1 | MA0073.1 | chr1:16277529-16277549 | CCACATACCACCACCCGCCA | + | 6.33 | | SP1 | MA0079.4 | chr1:16276264-16276279 | GAAGCCACGCCCCTC | + | 6.67 | | SP4 | MA0685.1 | chr1:16276264-16276281 | GAAGCCACGCCCCTCAC | + | 6.35 | | TFAP2C | MA0524.2 | chr1:16277366-16277378 | TGCCCTGGGGCT | - | 6.11 | | ZNF263 | MA0528.1 | chr1:16276035-16276056 | TTCTCTGCCTACTCCTCCTCT | - | 6.37 |
|
| | Number of super-enhancer constituents: 22 | ID | Coordinate | Tissue/cell |
| SE_01097 | chr1:16275403-16279590 | Adrenal_Gland | | SE_01987 | chr1:16272432-16279631 | Aorta | | SE_02709 | chr1:16274610-16280662 | Astrocytes | | SE_03452 | chr1:16275260-16277700 | Brain_Angular_Gyrus | | SE_04408 | chr1:16274061-16278759 | Brain_Anterior_Caudate | | SE_05249 | chr1:16273948-16279656 | Brain_Cingulate_Gyrus | | SE_06124 | chr1:16270812-16279644 | Brain_Hippocampus_Middle | | SE_07342 | chr1:16272948-16278751 | Brain_Hippocampus_Middle_150 | | SE_08131 | chr1:16272535-16279679 | Brain_Inferior_Temporal_Lobe | | SE_18522 | chr1:16273733-16281386 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19255 | chr1:16273419-16281362 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_27189 | chr1:16274173-16281550 | Esophagus | | SE_36664 | chr1:16274460-16277822 | HMEC | | SE_38820 | chr1:16274752-16281466 | HUVEC | | SE_40080 | chr1:16274659-16281418 | K562 | | SE_45001 | chr1:16274543-16280813 | NHLF | | SE_45986 | chr1:16274066-16281079 | Osteoblasts | | SE_47059 | chr1:16275327-16277770 | Ovary | | SE_55849 | chr1:16274274-16283539 | u87 | | SE_61132 | chr1:16274043-16303645 | HBL1 | | SE_64852 | chr1:16274416-16281190 | NHEK | | SE_67570 | chr1:16274274-16283539 | u87 |
|
| | 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 |
| GH01I015947 | chr1 | 16274011 | 16281336 |
|
Enhancer Sequence | AAATGTGTCA TCATTTCAAA AATGAAACGA CATGGTCACT TTAACATTTG TTACAAAAAG 60
AATGCATGAC AATCTCAGAA TAAAGGACAG ATGTTTCAAT TGGACATGTT GGTCTTTAAG 120
AAAACTTTCC TATTTTCTCA TTCTCTCATG GACAGGTGAA GACAAGACGG TGTTTCATCA 180
GCCAGTGTTG CAGAACTCGG CCCCTCTCAG GCTCTGCACG TACCCCATCC CCCGACAAAG 240
CCTAGCTCTC CCTCTCTTTC TGATTCATGG GAACTACCTA GAGTTGCGGA GTCTTCTGAC 300
TCCAGAAACC TGTGTCCTGG TGGCCATCCC AGGAGAAACA ACTTTGATCC TGACCCCAAG 360
AGCTGCTGAC CTGGCCACAA CTTCTCTGTC AAGGGCCTCA CTTAATGCCT GGAAATCCCA 420
CAAGTGAAAA TGCTCAGGAA AATTCCATGG CCCAGTGCCG AGCAGTCTTG AACCGCACAA 480
GCCGTGACTA AGTAACTATC TAAAACAGCT CTCCCTCCCG CCCCAACACC ACCCAGAGTG 540
GGCGTCAACA TCAGCAATTG TCTAGGGAAA ATAAGCGGGC CCTCTTTTCT AGAAAGAACC 600
CATTTCAGAA TGTTTGAAGA GAAAAATCAA CACCCACTGT CTGGGGCCAC ATTAGACAGA 660
TTCAACTGGG CACGGCTGTC ACGCCCTGGC CCAGGATCTG CTAAGGGGTA GTGAGTTCTC 720
TGCCTACTCC TCCTCTTCTC TGAGGCCTGA GTCTGCACGG GGCTGGCTCC CCGGCTTCTG 780
GGCAGGTGAG AGGGACACTT TGGGGCTCTC CGCCCCCAGT TTCGGCAGCT CTGCCCCGGC 840
TCAGGCACTC CCCTGTGACA TCAGCATCTT GGGGGGTGAA TCACTGCCGC AGCTCTGAAG 900
CTGCTGTGGC CATGCATGGC TGTCGGGCTG TGATGAGTCC GGAGGAAGCC ACGCCCCTCA 960
CACCAGCACA GGTCGGCCTT GAAGGGCGCC AAGGCCTCCC ACCACGTGAT GTCTGGAAAC 1020
TTTTCACAAG TGGGGGTATC TGCTGAGCGG GGGGAAGTGA CGCAACAAAT AACGGGGAGC 1080
ATGGCAGTGG CAACAGGCAT GAGCCACAGC GCACCAGCCT CCGAGCCACA AGTTCAGCGT 1140
TGCTGCTGCT GCCAGAGGCC CAGAAACAGC TGTTCCCTCC CCCTACACAT CCCCGCGCAG 1200
GCTTTGGCTC TCTCAATGAC ATTCCTAAAT GGCTGTGGCT AGAGCCCTAA GTGTAAGCAC 1260
TGGAGAGCCA GGGCCAGCCC CGAAATCAGG AGGTAAGGCC CTGGGGCAGC TGGCCCCGCA 1320
CCAAGTGCAC CAAGTGGCTG GCAGCAGCAC ACGGCCACCT GGAGCAAAGC ACAGAGGCCT 1380
TTCTCTCCTG TCCTCAGTCC CTGGAAGCAG CAGGTTCCTA TCTGTGACCT GAAGGAACGC 1440
AAGGGAGAAT CGTGGCTGCG CTGCTCCTAT GCACTGGACA TGGGGAGGCA CCAATGTCCA 1500
GCTTGTGGAT CAAGACCTGA AGGGCACAAA GGGCAAGGTG GGTGCAGAAG GAACCAAAGG 1560
CAGGGGCGAG GTGGGCCCAG GCCACGGCAA CCCTAGAGCT GTCTTCTCCT GGCTGTGGAA 1620
AAGGTCACGT GAGCACACAG GTGTGTGGGT GGCAAGCCCT GGGCCTCAAT TGCTAGTCAC 1680
CCCCTACATA CCCAGGAGCC CCAAGTGCAG AAGAGGGGAA TACCAGGGCC CACACAGGGC 1740
AAAATCCTCA ACTGGCTTCA GAAGCAGCCC ATCTGGAACT TGCAAGTGAG GCCCAACCCT 1800
TCTCTCCAGG CTGTGTGCCT GGCTTCCTCA CCTTCCCCAG GAGCCAACCC GAAACTTGAG 1860
CCACCCAGGT GCTAAAACAA CCTGGGGAGC ATCAGCTGAA CCCCCAGAGG TACAAAGAAC 1920
CCTCTAGCAG GAAAACCATC TGACTTGCCG GGAAGAGACA TGTGAGGAGA CTCCTAGCCA 1980
AGGGGAGGGA CAGGATCAAT CCCCTTGTGT GGGCCCAAGG CTGGGATGAG CCTCCCTGTG 2040
GCCATGTGCC CTGGGGCTTC CTGGCAAGCG CAGCCCCGCC CAGCCATACA GCTGTCCTGG 2100
GACTGGATGG ATGGATGGAT GGGTAAGCTA GATAGATTAG ATAAGACACA TTCGCTAGAT 2160
AATAAAATAG TAAAGGCCCC AAGGACAGGG TGGGTGGTGG CCCAGCCCCC CACATACCAC 2220
CACCCGCCAA GAGAGCAGCT GTGTGCCCAT GAGCAACATT TTCCACCGTG CTGACTGCAC 2280
TTTTCCAATG CAAGATGCCC GCCCAGAAGT GGGCTCCTCC CACACACGGG TGTTAGGAGG 2340
AGAAACAGAG GCGTCTATAA TCCTCTGAGG 2370
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