| Tag | Content |
|---|
EnhancerAtlas ID | HS193-00387 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr1:19723960-19727050 |
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 | chr1:19725163-19725174 | CTGAGTCACCC | - | 6.02 | | JUNB | MA0490.1 | chr1:19725163-19725174 | CTGAGTCACCC | - | 6.02 |
|
| | Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
| SE_01631 | chr1:19723726-19729381 | Aorta | | SE_04046 | chr1:19724370-19725207 | Brain_Anterior_Caudate | | SE_05833 | chr1:19726303-19729509 | Brain_Hippocampus_Middle | | SE_18410 | chr1:19723442-19725319 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_18410 | chr1:19725443-19729168 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_25786 | chr1:19726004-19729195 | Duodenum_Smooth_Muscle | | SE_26537 | chr1:19724151-19725529 | Esophagus | | SE_26537 | chr1:19725748-19729360 | Esophagus | | SE_28668 | chr1:19726413-19727893 | Fetal_Intestine_Large | | SE_31447 | chr1:19724153-19725439 | Gastric | | SE_42185 | chr1:19723995-19725245 | Lung | | SE_42185 | chr1:19725760-19727652 | Lung | | SE_45720 | chr1:19723558-19729015 | Osteoblasts | | SE_46635 | chr1:19724365-19725479 | Ovary | | SE_46635 | chr1:19725782-19726317 | Ovary | | SE_46635 | chr1:19726583-19727639 | Ovary | | SE_48688 | chr1:19726341-19727652 | Right_Atrium | | SE_50058 | chr1:19723750-19725541 | Sigmoid_Colon | | SE_50058 | chr1:19726388-19729383 | Sigmoid_Colon | | SE_51211 | chr1:19724128-19725260 | Skeletal_Muscle | | SE_51211 | chr1:19725539-19727979 | Skeletal_Muscle | | SE_52345 | chr1:19723725-19725612 | Small_Intestine | | SE_52345 | chr1:19725640-19727680 | Small_Intestine | | SE_54550 | chr1:19726107-19728569 | Stomach_Smooth_Muscle | | SE_65446 | chr1:19724311-19725380 | Pancreatic_islets | | SE_65446 | chr1:19726450-19727081 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 19724618 | 19725348 | | chr1 | 19724035 | 19724400 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I019397 | chr1 | 19723770 | 19729243 |
|
Enhancer Sequence | ACCCTAAGGC CGTGCGGACT CTAGAATGAC ACCTGGTGAG TAACCTAGCA GGCAAAATAA 60
TTCAGCTGAA AGAGTCACCA GCTGGATGGT GGCAGAGAGA AGTACTTGGC AAGATTGGTT 120
TTTCACACAA GGTCAACGCG AACGGAACCT CTCATACCAG CCACCTACTA GGGTACAGCA 180
TCAAGACCTA ATTTCAGGGA GGGAAATGGG AAATGCATCC ATTTCATCAT CACTGGATAC 240
TAAGGGTTAG GCCTGGCCTC AGGCTTTATA AACCACATGT GTGCCAAATG TCCACGTCTA 300
AACCTAGAGT TTAGGGTGAA AACTATGAAT GGGCTACCAT GGAAGTTACA AAATAAGAAT 360
GCAGGGGGAA GCCTGAGGGC GCGCGCCACC CGAATGCGGG AGGAGCCAGA TGGGGCAGCA 420
TAGGAAGGGC TGTTCTTTAC CACTGATCTG GGGGGCTCAT GATCGCCCAG AGGGACAGAC 480
CAACAGCATC GGGGTCTGTG GGTTGATATT CATCTGCACG TCGACACTGG TGGGGATGCC 540
AGGGAAATCT CACATGTTCT GTTTAGCAGA AACGAGACAC CTGAGGCAGA AAGTGACAAT 600
AAGGAGTCAC ACGGCCAGGC AACCATGGGC AATGGCAACG CAGGGGATAC TTTAGAATCT 660
GAAAGCCTGT GAAACACCCT CAAGTCCGAG AGGATCTGCT CCATGATGAG GAACTCCGTG 720
ACCTCCAGGG CCCACACACG GAGGTGAGCC ACAGTCATCC TGCCACACCT GCTCAGTCTC 780
CCGATGAGCC AGGCGAGGTG CTGAGCCCTG TACTCCTCGC CCCAGGGGTC CTGATAGCCC 840
CTTGGGAGGC GAATGACCTT TGAAGCCACA GCAGAGGCTG ACCAGCTCAG AGCACGGAGC 900
CACTGAGTCA GAGGGCGGAG GTCTGGCTTC CTCCAACAGA TTCTCCAAAA ATCCTCACGA 960
TCACAAGCTT CTAAACCTCC ATGACCTACC ATGATTCCAG TAATACTTCT GTTTCCCTTC 1020
AAGTGGGAGT GTTTGTGCCA TGTTTACGTG TCTGAGTGGG GGAGCGGGTG CTAAGGCAGA 1080
CTCAACAAGT CGGGTTGCTT CGCTGTTCTC AGCACAAAAG TCACCCAGGC TGTCTGGCCA 1140
CAATGTTTCA CACTGGATTC CTTCCACTGG AGGGATGTCT CATCAGGTTT TGCTGTAATT 1200
TCACTGAGTC ACCCATAGAA ACGACCAAGC AGGGGAGACT GGAGGGGACA TCTCCAGGGG 1260
GCCACATCTG AGCTGAGTTA CAGAAAGTGA GGCAGGGCTG GCAGTTAGGG CAGGTCGCAA 1320
AGCAGCCCAA GGACTAAGGT GCAGACAGAG AGCATCTCTG TCTGTCAAAG GCAGACAGCG 1380
TGGGATGCCG AATGCTGATA GCTGCACAAC TCTTTTTTTT TTTTTTTGTC ACCCAGGCTG 1440
CAGTGCAATG GAGCGATCTC GAGTACCGCA ACCTCCGCCT CCCAGGTTCA AGCAAGTCTC 1500
CTGCCTCAGC CTCCCGAGTA GCTGGGACTA CAGGTGCTTG CCACCATGCT TGGCTAATTT 1560
TTTTATTTTT TAGTAGAGAC AGGGTTTCAC CATGTTGGTC AGGCTGGTCT TGAACTCCTG 1620
GACTCAAGTG ATCCGCCTGT CTTGCCCTCC CGAAGTGCTG GGATTACAGG CATGAGCCAC 1680
CATGCCCAGC TAGCTGCACA ACTCTTGCGT GTGCTAAAAA CCATTGGACC GTACACTTTA 1740
AAAGTGTAAA TGTTATGTTA TGTGAATTAT ATCTCCAGAA AGCTGTTGTT AAGAAGGTGA 1800
ATCAAGAGAG GATATTTTAG GCAGAGAGAA CCACATGGAT CCAAGACATC ACAGGTAGAC 1860
ATCCAGGAAA CCAACAGTTT CAGAATACGA GTACGTCATG TGACCCAGAG TTAGGTTGGT 1920
AAAAAGTGAC CCTGGGTGTC AGGAACCATG GGCAGTGTTG TCTTTCTCCT CACTCTCAGT 1980
CGTAGCTGTT TGACTCTTCA CTCTTACTAC CCAGAGCTTT TCCTACATCA AAATAAACCA 2040
AGGTACTGCA GGGACTTGCC ACTGGCCTGG AAGTCAGAGC TGGTTCTGCC ATGAAACGGT 2100
GCTACATGGG GCATGGGCCA CAGCTCCCTG GTCTCTGCAA TGGATGGTTC TCTGAGAGAG 2160
GAGCACTTTG AGGGCTGTGA GTACAGAGGG AGGAGCTCAG GGTGTCAAGA GTGGGAGAGG 2220
AAGTCTGGGC CTACCACCTT CTACCTGGTT TATTCAAGTT CTAAGATTTT GCTTAAAAAA 2280
AGGGCTGTAC CAATTTTCCA AATGTTTGAA AACCACTAGA TGAGATAATC GGTAAGGTTC 2340
ATTTTAGTGT TGACATCCTA CGAAGTTTCA TAGTTCAAGA CTTGAGAGTT ACTCAAAAGT 2400
TTGTGTCATC CCTCCTAAAA CAAACCTTTA CTAAGCAAGG TACTCTGAGG CTCAAACCAA 2460
CTGTGGACTG CCCAGCTCTT CGGTTCACAG CCTTAGGACA CAGATGCAAG CAGCTGAGTG 2520
AGTTATTCAC AAGAAGGGGA AGAAGGAAAA GGCTTGGAAC CCATAATCTT CTCCCCTGAA 2580
TGCCATGTTC AAATTTAAAC TCTTAGGGAA TTTCTATATT TGTATACAGA ATCCAAATTC 2640
CCTTCTCTTT TCTCTTCCAG GAGAGATTCC GAGCCCACCC CTTGCCTGCC TCCGAGACCT 2700
CAACACCATC CTGCTTACTA AAGGGAGCCC AGTTTTTCCC GCTACCCATG GCACAGGTCT 2760
TCGTCAATTT CAGTGTGCCC TTCATGAATC TGGCATGTGG TCACTGGCAG TTAAAGGGGG 2820
TGATGATGGA GAGGAGAAAC CCCAGGCTCC AACTACAAAA CCCTGCGGGA CACGCAGGCT 2880
CCTCTGGGCT TCCCGGCCCA CATTCCTGGC CTATTTCAAA CATCAGGGAA GCAGACTGAG 2940
CGTGCCATGC CCTCCTCAAG TATTTTTAAC CTGTTTCCAA AACCAGACAT GTTCTAAGGG 3000
GGGCGACCCA GGAATTCCTC ATCCAGGGCC AGTGCCTGCC AACCGCGAGA TGTTGGCTTT 3060
CTAACAGCTC TGAGGAGGGA GTTGTTGTCT 3090
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