| Tag | Content |
|---|
EnhancerAtlas ID | HS040-19212 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr2:20430610-20433710 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr2:20431539-20431550 | CCACACCCTCC | + | 6.32 | | Klf1 | MA0493.1 | chr2:20431537-20431548 | AGCCACACCCT | + | 6.02 | | POU2F2 | MA0507.1 | chr2:20432857-20432870 | ATATGCAAATTCA | - | 6.67 | | ZNF263 | MA0528.1 | chr2:20431270-20431291 | GAAGGATGAAGGAGAGGAACA | + | 6.43 | | ZNF263 | MA0528.1 | chr2:20432100-20432121 | AGGGGAGGGGCGGGGGGGGGG | + | 6.75 | | ZNF263 | MA0528.1 | chr2:20431267-20431288 | GGAGAAGGATGAAGGAGAGGA | + | 6.89 |
|
| | Number of super-enhancer constituents: 20 | ID | Coordinate | Tissue/cell |
| SE_02914 | chr2:20430841-20431728 | Bladder | | SE_02914 | chr2:20432323-20432755 | Bladder | | SE_23108 | chr2:20430728-20433031 | Colon_Crypt_1 | | SE_23761 | chr2:20430771-20431844 | Colon_Crypt_2 | | SE_23761 | chr2:20431878-20432712 | Colon_Crypt_2 | | SE_24805 | chr2:20430733-20432995 | Colon_Crypt_3 | | SE_26530 | chr2:20430669-20434103 | Esophagus | | SE_31478 | chr2:20430789-20432802 | Gastric | | SE_33954 | chr2:20430757-20433179 | HCC1954 | | SE_35878 | chr2:20430227-20437683 | HMEC | | SE_42432 | chr2:20430732-20431952 | Lung | | SE_42432 | chr2:20431959-20433013 | Lung | | SE_50296 | chr2:20430643-20431888 | Sigmoid_Colon | | SE_52465 | chr2:20430618-20432815 | Small_Intestine | | SE_56896 | chr2:20430348-20431529 | VACO_400 | | SE_56896 | chr2:20431583-20433112 | VACO_400 | | SE_57761 | chr2:20430451-20431506 | VACO_503 | | SE_57761 | chr2:20431527-20433114 | VACO_503 | | SE_58069 | chr2:20430905-20431840 | VACO_9m | | SE_64257 | chr2:20430356-20433549 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr2 | 20430848 | 20432571 | | chr2 | 20430665 | 20430761 | | chr2 | 20431248 | 20431615 | | chr2 | 20432677 | 20432919 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I020230 | chr2 | 20430368 | 20437558 |
|
Enhancer Sequence | TGGCAGCTTC AAAGCTCTCT CTGCTCCATC TTCACATTGC CTTCTTCTCT GTGTATAGTG 60
AAATCTCCCT CTGGCTGTCT CTTGTAAGAA TACAGGACTG CATGCAAGGC CCACTGGAAT 120
AATTCCCAAT AATCGCCCCT ATCTCAAAAT TCTTAATCAC ATCTGCACAT CTGCAAAGAC 180
CCACCACCAC CACCTTGTAT TGGTTGTTGT TCTATAAGTT AACATTCACA GGCTCCAGGG 240
GCTGGGATAT AGATATCTTT TAAGGGTAAT TATTCAGCCT ACCGCAGGCA GATAGAGCAG 300
GGAAAGGACA TTCCAAACAG GAAACCCAGC AAAGAGCAGG CAAAGAAGCA AGACAGAGCT 360
TCAGGATGTT CAGGAACTGG AAGGAGTCTG AGGTGGGCTG GACTGGCCGG GGCACAGGAC 420
CTCTGGCAAG GGCTGGATCA GAGGGAGAGA GCCTGAGCAG TGTGTGCCAG TAACGGGCCG 480
TGCCTAGGCT GGAGGAGCCA GTGGTTTGCA TTTTGAAAAG ATCCTCTGGC CACTGTGCGA 540
AGGGCAGGCT GCAGGGAGGG AGACTGTGGG CTGGGACACC CTATGCAGGG GCCGTGAAGG 600
TACAATGTGG GGAGCCAGGA TTGAATAATA TGGAGGAGGT GGGATGCGAT GAGGCTTGGA 660
GAAGGATGAA GGAGAGGAAC AGTGCAATGT GGAAAATCCT TGGTGAGGGT CCATTTCCAC 720
CTGGTTTACG TAAACAGCTA GCGTCAGAGG GGCCGAATCA GTGTGTAAAG TGGCTGCCTA 780
GGCTGGGGCA GCACTGGGTG CTGAAGTCCT TTGGTAGATC ACCCCGGGGC TCGTGACTCA 840
GTTCTAGGCT GCCTCAAGGA TGAGCCTTTG TTGCCTTTGT TGGAAGCTTG GACAGGAAGC 900
TCTCCAGCAG GGAGGAGTGC CAACACCAGC CACACCCTCC CAGGTGCAGC TAGGCCCAGT 960
CACCCTGAGC AATTTCCTGG AGTGAGGCCA CTCGCCACTG GCTCACACTA GCCCCTGCCC 1020
TGCAGGGCAT CATCAAGGAT CTGGAGTCTG AGCAGCACCA GGCTCTCTGT GACTCAGCCC 1080
CTGTGGGGAA GGGGAGCCCG TGCTGGTGCT CTTCGGGCTG GAGCAGGGAA GTAGCTCCCC 1140
CTGTCCCACC TCACCTGCTT TGCTAGGGAC AGACTTTTTT TTTTTTTTTT TTTTGAGACA 1200
GAGTCTTGCT CTGTCACCCA GACTGGAGTG CAGTGGCACA ATCTCGGCTC ACTGCAACCT 1260
CCACTGCCCG GGTTCAAGTG ATTCTCCTGC CTCAGCCTCC TGGGTAACTG GTATTACGGG 1320
TGCCTGCCAC CACACACGGA TAATTTTTGT ATTTTTAGTA GAGATGGGGT TTCACCATGT 1380
TGGCCAGGCT GCTCTTGGAC TCCTGAGCTC AGGTCATCCA CCCGCCTTGG CTGCCCAGGG 1440
ACAGACTCTA CAAAGCCCTG CTAATTGCTG CATGCAATAT GCTGTTTGTG AGGGGAGGGG 1500
CGGGGGGGGG GGAGCTGGGA GGAGTTGTTG TTGTTTTGAT TTTTTTTGAG ACAAGGTCTC 1560
ACTCTGTCAC CCATGCTGGG GTAGTGCAGT GACGTACATA ATCACAGCTC ACTGCAACCT 1620
CTGCCTCCTG GGCTCAGGTG ATCTTCCCCA CCCAGCCTCC ACAGGCACAT ACCACCATGC 1680
CTGGCTAATT TGTGTATTTT TTGTAGAGAT GGGGTTTTGC CATGTTGCCC AGCCGGTTCT 1740
TCTACACATT CTTTGAGCTA CTTTAGCTGT GTGACTTCAG GCAAGCAGTA ACCTCTTTGC 1800
TCTTTAATTT GTTCCTCTGT GAATTGGAGA AATACTAGTA CCTACCTCAA AGAGTCAAAA 1860
GCATTGAATG AGCTAAGCCC TCCATAGGGC CTGGCACACA CGTGTAAGTG CCCCCTGCAT 1920
GCTAGTGATG CCGTGGATAC CCACAGTGGG ATTCACTGGG AGAGGCAGAT AGACTCATTT 1980
TAGGCAAGTT CCTAAGCATT CTGACATAAT ACATATAAAA CACTTAGCAC TTTACCTGGC 2040
ACAAGGTAGG ACCCTAGAAA TCATAGAGAA GTTGGAGATT CTAAAGCCCG CAGGGGAGAA 2100
TCTGGGCTGG GCTCTGAAGA GATTCCTGAG CTCACCGCAG CCAGGATGTA TAAGTCATAG 2160
TGTTATGTCA GCGCTCATAC CTGTGTGTAG CACATGTGCA CGCACCTTCA CGCACACAGG 2220
TGTGCCTCAC CTCCAGCCCC AGGATGCATA TGCAAATTCA TGTAACAGAT GAGTAACTGA 2280
GTTCACTCAA CAGGTGAGAA AGTGACTTTG CATTCCCTAG GAATGGGACA GAGGTTGCAA 2340
AGGGACAGCC CCTAGGGCTG CATTTGGCCT GTAGAAGTGT TTTGCCTTTA AACTATTTTA 2400
TTTTGTTTTC TTTTTTTTGT TTTTGTTTTC CCCTTATGCT ATTTTTTTTT TTTTTTTGAG 2460
ATTGAGTTTC GCTCTGTCAC CCAGGCTGGA GTGCAGTGGC ACAATCTCGG CTCACTGCAA 2520
CCTCTGCCTC CTGGGTTCAA GTGATTCTCC CGCCTCAGCC TTCCGAGTAG CTGGGACTAC 2580
AGGTATCCGC CATCACACCC AGCTAATTTT TGTATTTTTG TAGAGATGGG GTTTTACCAT 2640
GTTGGCCAGG CTGGTCTTGA ACTCCTAACC TCAGGTGATC TGCCTGCCTT GGCCTCCTAA 2700
AGTGCTGGCA CCCAGCCTAC ACCATTTTAA AAAGGAGATT TCCATCGGAG AATTGCATGT 2760
AAGAATCAAG ATTTCTGACT TTTCGGCCAG GTGTGGTGGC TCACGCCTGT AATCCCAGCA 2820
CTTTGGGAGG TCGAGGCAGG TGGATCGCCT AAGGTCAAAA GTTTGACACC AGCCTAGCCA 2880
ACATGGTGAA ACCCCGTCCC TACTAAAAAT ACAAAAATTA GCCGGGTGTG GTGGCAGGAG 2940
CTTGTAATCC CAGCTACCCG AGAGGCTGAG GCAGGAGAAC CACCTGAACC CGGGAGGCAG 3000
AGGTTGCAGT GAGCCGAGAT CGCACCACTG CACTCCAGCC TGGGCGACAA GAGCGAAACT 3060
CTGTCTCAAA AAAAAAAAAA AAAAAAAAAA TTCCGACTTT 3100
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