| Tag | Content |
|---|
EnhancerAtlas ID | HS038-13930 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr22:50340160-50342500 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr22:50341971-50341981 | GCCCCGCCCC | + | 6.02 | | PLAG1 | MA0163.1 | chr22:50340609-50340623 | GAGGCCCAAAGGGG | + | 6.37 | | PLAG1 | MA0163.1 | chr22:50341608-50341622 | GGGGGCCACGGGGG | + | 7.1 |
|
| | Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
| SE_03028 | chr22:50341487-50344026 | Bladder | | SE_17545 | chr22:50337358-50341301 | CD4p_CD25-_CD45RAp_Naive | | SE_17909 | chr22:50337253-50340777 | CD4p_CD25-_CD45ROp_Memory | | SE_23129 | chr22:50340142-50347336 | Colon_Crypt_1 | | SE_23738 | chr22:50340192-50347293 | Colon_Crypt_2 | | SE_24687 | chr22:50340156-50348528 | Colon_Crypt_3 | | SE_26808 | chr22:50341423-50346477 | Esophagus | | SE_28169 | chr22:50340100-50347261 | Fetal_Intestine | | SE_29459 | chr22:50340194-50347426 | Fetal_Intestine_Large | | SE_31381 | chr22:50340030-50364844 | Gastric | | SE_34375 | chr22:50340613-50344021 | HCT-116 | | SE_35007 | chr22:50341530-50344029 | HeLa | | SE_35554 | chr22:50341650-50344088 | HepG2 | | SE_41617 | chr22:50340249-50340536 | LNCaP | | SE_41617 | chr22:50341850-50344223 | LNCaP | | SE_42159 | chr22:50339996-50364887 | Lung | | SE_47471 | chr22:50340157-50349301 | Pancreas | | SE_50117 | chr22:50339205-50347666 | Sigmoid_Colon | | SE_52469 | chr22:50340730-50346981 | Small_Intestine | | SE_56937 | chr22:50340142-50346911 | VACO_400 | | SE_57421 | chr22:50341953-50344030 | VACO_503 | | SE_58096 | chr22:50340895-50342014 | VACO_9m | | SE_58096 | chr22:50342032-50347148 | VACO_9m | | SE_61206 | chr22:50315437-50364432 | HBL1 | | SE_61985 | chr22:50315627-50364432 | Toledo | | SE_62450 | chr22:50318672-50364388 | Tonsil | | SE_65335 | chr22:50340176-50344048 | Pancreatic_islets | | SE_68380 | chr22:50327316-50364640 | TC32 | | SE_68381 | chr22:50327316-50364640 | TC32 | | SE_68382 | chr22:50327316-50364640 | TC32 | | SE_69071 | chr22:50340249-50341775 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 50340250 | 50341213 | | chr22 | 50340274 | 50341177 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I049942 | chr22 | 50336159 | 50349619 |
|
Enhancer Sequence | TTACAGAAAA AAGAACGAGC TTCGTACGTT AGCACCTATA ATATCATTTC ATCCTGCATT 60
TTGAACAATG AACCCTGAAT TCTCATGTGC GCTGGGCTCT GCAAATCATG TGGCTGCTCC 120
CCATAGTCAG GAAGGAGAGT GGGACTCAGG GGAGGAGGCA GGATGAGCTG AGACCCAGGC 180
TGCCTGTCCC TACCACTGAC CAGGACAGCG TTCCAGCCTC CCCGTCTGCT CAGAATCTGC 240
CCTGACCTGC TCCACACCCC CGCAGGCCCG CAGGGGAGGG CAGAACTAGA AGGGACCAGC 300
GCATAGGGAC CTGGGGGTGC TGGCACTGAG GTCTCTGGGC CTGGGATGCT GACCTTCCCG 360
GAGCCCTGAG CTGGGCCAGG ACGAGGTCTT CCCATCAGAC TTGCCGCTGG CTAGGTGACC 420
GGCCTGTCTC ACAGATGAAA ATATATTCTG AGGCCCAAAG GGGGCCCAGA CCCTGACTTT 480
GTGGCCCAGA GCCAGGTTCT CCCCATAACC AGCAGGCTTC TTTACCCACA GGCCACTGTC 540
CACCCAAGCC CCGCAGGCAG GAACCCTTGG TATTGGGTGG CCCTGAGCTT GGGATTTGCC 600
GCTGGCTGTG TGGCCCTTCG GAGCCAGTCC GGCACACCCG CAGGCACACA CACATGCGCA 660
CTCGCATACA GCCACAGATT ACACAGGCAC CAGCTTCCCG GGAATCCATT TGTCATGCAA 720
ATGCCCCTCC TGGGGCCCCT TGCCTCCCCA GAGCTGTGTC TGTCCAGGGT GGGGCCCAGG 780
TCCGTGGAGT CCTGCAGTTT CCTGGCCACA GCTATTGGCA ACTGAGGGAT GTCTCTCCAA 840
AGAGGACCCA GATCCACGTC CAGGCTTGCC TGGGACCCGA TCCCTGCCCA GTGCGGGGGC 900
TGCAGCCTCA AGGCCCAGTC TGGCCACCGC CAAGTCCACT GGGAGCCAAG TGTGGGTTCA 960
TTCCCTCGTG GCTTCTGGTG CACCAGTGGG GTGGGGGGCC AGGCCTCTTT CCCTCCTTGG 1020
CTGCCTCAAA GCAAGAGGGA GGGACTCTCA GCCCTGTGCC CACCGACAGG CCCAGTCTCC 1080
ATTCCTCCTA AAGCCCCTCT ATGGCCCCCC AGCCCTTGGA GCTGAGCTTG TGAGAGCCGT 1140
CCCCTACAGG GTGGGCTCGG GAGGCAGAGC TGTGAGCCTG CTCCCCGCCC ACCCAGAGCC 1200
CAGCTGGGGC AGACCCAGGC ATCCAGGCCG GCAGGGTGAG CCTGTGCCCA GGTTGGGCAG 1260
CCCCCTATGC TGGGGGTGGC CAGGCTCTGG GCCTAAGTGC TGCCGGGAGA CAGGGTGGCT 1320
GGGCTCTGGG ATGCTGGCTG AGGGACACAG GCTCCCTCCT GTCCTCCGGG GCCAGTGGAC 1380
CCTGGGGCAG CCCCCATGCC TGCTGTCCTG TCCCCACACA GCCTGTGAAG CAGGCTCCAG 1440
GCACACATGG GGGCCACGGG GGCAGGTGGT CCAGACGGCT CTCAAGGCAA AGCTGGGAAC 1500
ACTGTCCCAT CCCTCTGGAA CCCGCCCTGG TGAGGGGTGC AGGGGCCCTC AGTGGCCACC 1560
TTATAGGACC GGGCACCGGG CACTTCATGA GGCTGTCTGC TCGGCCACAG CAGCCCTGCT 1620
GATGGAAGCC AGCCCTGGGC CCACTGCAGC TGAGCCACCC AGGGGCCTGG CCACCCAGAG 1680
CTTCCCTGAT AGGCTGCGCT GTGCCCGGAG CCCCCCAGTG ACTGTCTCCT GCCCAGCCAG 1740
GTCCCAGACC CAGGGCAGCC TGCAGGACCC CAGGCCTCCA CTCCCGCCAC CTGAGTGTCT 1800
GTTCTGCATC TGCCCCGCCC CTGCCTACTG GCAGCCGCAG CCCTGGGCGG GCCTCAGCCG 1860
TCGGCTTTCT CAGGGTGTCT GGGTTGGGGC GGGCAGAGCT GCCCTCTGGG GGTTCCCGTG 1920
GTCCCCTAGA GGGTGGGCTC AGCGGCATCA GCTGCCAGAG AGGCTGACCG GCCCTCATGG 1980
CTCTTGACGG TATGTGCAAG AGTTTGCCTG GCGTGGTGGG GGGTGTTGCT GGCCAGGAAC 2040
TTTCTTGCCA TCGTCTTTCT TGGTGTCTGT CTCCCCTGGG TTCTCTGGAC CCTGTCAAGC 2100
CTGTATGCTG AGGGTATGCT GTTACCAGGT GGCAAGGTGT CTCAGGCACT CCTTCAGGGT 2160
GAGCAGTCAG CTCCTGCTGC TGCCAGGGCA GAGGTGCAGA GAGCGGGGAG CAGCTGGTGG 2220
TGCCGGAACC CACAGCAAAC CCCCCGCCCT CCAGCCCTGC CCCTGACACA CCCCCGATGG 2280
CCTGGCGGAG CATCCCACCA GCCCAGCAAG AGGGCTCCTC TCCTCACCTG CCCAGGTCCC 2340
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