| Tag | Content |
|---|
EnhancerAtlas ID | HS098-00688 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr1:19724300-19727670 |
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 | 19726589 | 19727226 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I019397 | chr1 | 19723770 | 19729243 |
|
Enhancer Sequence | GGAAGTTACA AAATAAGAAT GCAGGGGGAA GCCTGAGGGC GCGCGCCACC CGAATGCGGG 60
AGGAGCCAGA TGGGGCAGCA TAGGAAGGGC TGTTCTTTAC CACTGATCTG GGGGGCTCAT 120
GATCGCCCAG AGGGACAGAC CAACAGCATC GGGGTCTGTG GGTTGATATT CATCTGCACG 180
TCGACACTGG TGGGGATGCC AGGGAAATCT CACATGTTCT GTTTAGCAGA AACGAGACAC 240
CTGAGGCAGA AAGTGACAAT AAGGAGTCAC ACGGCCAGGC AACCATGGGC AATGGCAACG 300
CAGGGGATAC TTTAGAATCT GAAAGCCTGT GAAACACCCT CAAGTCCGAG AGGATCTGCT 360
CCATGATGAG GAACTCCGTG ACCTCCAGGG CCCACACACG GAGGTGAGCC ACAGTCATCC 420
TGCCACACCT GCTCAGTCTC CCGATGAGCC AGGCGAGGTG CTGAGCCCTG TACTCCTCGC 480
CCCAGGGGTC CTGATAGCCC CTTGGGAGGC GAATGACCTT TGAAGCCACA GCAGAGGCTG 540
ACCAGCTCAG AGCACGGAGC CACTGAGTCA GAGGGCGGAG GTCTGGCTTC CTCCAACAGA 600
TTCTCCAAAA ATCCTCACGA TCACAAGCTT CTAAACCTCC ATGACCTACC ATGATTCCAG 660
TAATACTTCT GTTTCCCTTC AAGTGGGAGT GTTTGTGCCA TGTTTACGTG TCTGAGTGGG 720
GGAGCGGGTG CTAAGGCAGA CTCAACAAGT CGGGTTGCTT CGCTGTTCTC AGCACAAAAG 780
TCACCCAGGC TGTCTGGCCA CAATGTTTCA CACTGGATTC CTTCCACTGG AGGGATGTCT 840
CATCAGGTTT TGCTGTAATT TCACTGAGTC ACCCATAGAA ACGACCAAGC AGGGGAGACT 900
GGAGGGGACA TCTCCAGGGG GCCACATCTG AGCTGAGTTA CAGAAAGTGA GGCAGGGCTG 960
GCAGTTAGGG CAGGTCGCAA AGCAGCCCAA GGACTAAGGT GCAGACAGAG AGCATCTCTG 1020
TCTGTCAAAG GCAGACAGCG TGGGATGCCG AATGCTGATA GCTGCACAAC TCTTTTTTTT 1080
TTTTTTTGTC ACCCAGGCTG CAGTGCAATG GAGCGATCTC GAGTACCGCA ACCTCCGCCT 1140
CCCAGGTTCA AGCAAGTCTC CTGCCTCAGC CTCCCGAGTA GCTGGGACTA CAGGTGCTTG 1200
CCACCATGCT TGGCTAATTT TTTTATTTTT TAGTAGAGAC AGGGTTTCAC CATGTTGGTC 1260
AGGCTGGTCT TGAACTCCTG GACTCAAGTG ATCCGCCTGT CTTGCCCTCC CGAAGTGCTG 1320
GGATTACAGG CATGAGCCAC CATGCCCAGC TAGCTGCACA ACTCTTGCGT GTGCTAAAAA 1380
CCATTGGACC GTACACTTTA AAAGTGTAAA TGTTATGTTA TGTGAATTAT ATCTCCAGAA 1440
AGCTGTTGTT AAGAAGGTGA ATCAAGAGAG GATATTTTAG GCAGAGAGAA CCACATGGAT 1500
CCAAGACATC ACAGGTAGAC ATCCAGGAAA CCAACAGTTT CAGAATACGA GTACGTCATG 1560
TGACCCAGAG TTAGGTTGGT AAAAAGTGAC CCTGGGTGTC AGGAACCATG GGCAGTGTTG 1620
TCTTTCTCCT CACTCTCAGT CGTAGCTGTT TGACTCTTCA CTCTTACTAC CCAGAGCTTT 1680
TCCTACATCA AAATAAACCA AGGTACTGCA GGGACTTGCC ACTGGCCTGG AAGTCAGAGC 1740
TGGTTCTGCC ATGAAACGGT GCTACATGGG GCATGGGCCA CAGCTCCCTG GTCTCTGCAA 1800
TGGATGGTTC TCTGAGAGAG GAGCACTTTG AGGGCTGTGA GTACAGAGGG AGGAGCTCAG 1860
GGTGTCAAGA GTGGGAGAGG AAGTCTGGGC CTACCACCTT CTACCTGGTT TATTCAAGTT 1920
CTAAGATTTT GCTTAAAAAA AGGGCTGTAC CAATTTTCCA AATGTTTGAA AACCACTAGA 1980
TGAGATAATC GGTAAGGTTC ATTTTAGTGT TGACATCCTA CGAAGTTTCA TAGTTCAAGA 2040
CTTGAGAGTT ACTCAAAAGT TTGTGTCATC CCTCCTAAAA CAAACCTTTA CTAAGCAAGG 2100
TACTCTGAGG CTCAAACCAA CTGTGGACTG CCCAGCTCTT CGGTTCACAG CCTTAGGACA 2160
CAGATGCAAG CAGCTGAGTG AGTTATTCAC AAGAAGGGGA AGAAGGAAAA GGCTTGGAAC 2220
CCATAATCTT CTCCCCTGAA TGCCATGTTC AAATTTAAAC TCTTAGGGAA TTTCTATATT 2280
TGTATACAGA ATCCAAATTC CCTTCTCTTT TCTCTTCCAG GAGAGATTCC GAGCCCACCC 2340
CTTGCCTGCC TCCGAGACCT CAACACCATC CTGCTTACTA AAGGGAGCCC AGTTTTTCCC 2400
GCTACCCATG GCACAGGTCT TCGTCAATTT CAGTGTGCCC TTCATGAATC TGGCATGTGG 2460
TCACTGGCAG TTAAAGGGGG TGATGATGGA GAGGAGAAAC CCCAGGCTCC AACTACAAAA 2520
CCCTGCGGGA CACGCAGGCT CCTCTGGGCT TCCCGGCCCA CATTCCTGGC CTATTTCAAA 2580
CATCAGGGAA GCAGACTGAG CGTGCCATGC CCTCCTCAAG TATTTTTAAC CTGTTTCCAA 2640
AACCAGACAT GTTCTAAGGG GGGCGACCCA GGAATTCCTC ATCCAGGGCC AGTGCCTGCC 2700
AACCGCGAGA TGTTGGCTTT CTAACAGCTC TGAGGAGGGA GTTGTTGTCT GCCTTTTCTG 2760
GCACGTGGGG AAGTGGGATC TCTCTCCAAT TCACTTTTAC GTCTCACATT TCTCATCAAC 2820
CAGAGGGCAG GATCTAACTT AAAGTGAGAG TCTTCAGACC ATCCTCAATG GAAGCTCTCC 2880
AAACACTGTT CTCCGGCTTC CAACAACAAC AGGAGTCCAT AAGGTTCCCC AAATGAAGGA 2940
CCTGGATAGA TCTTGTAGGA AAAAAAATCC TATGAGGACA AGGCCAAGGA ACGGGCCTAT 3000
ATGCACTTCA CTTGAATTAT GCCTCCTGGC TCTAGGTGAC AAGAGCCATC TTTTTCACCA 3060
CTGGAGAGCT CAGCCTCCTA CCACCTTGCC CCGATCCTGA CCTGGTTCAG ATTCCTCGCT 3120
AACATACTTC TCTCACCTTG TAGCACTGTT GCACATTGAA CAGGAGGGAA AAGCTCTTTT 3180
GTTCATTTTC CTTAGAATGG AACCAAAATG ATACTCCAGT AGCTCCATCT AAAAGCTCAA 3240
GTGGCAGCTA ACAGCACGGA CACCAGGGGC ATCCCTTGCC AGCTTCCAAT GCCATGGTGA 3300
GAGACACTCA TCATGGTTTA AAAAAAGACC AGAGAGCATT TTCACAAGCA ATTCCTAAGA 3360
GACTTAAATT 3370
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