| Tag | Content |
|---|
EnhancerAtlas ID | HS040-34689 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr9:93954290-93956860 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr9:93955577-93955589 | GCTATTTTTAGC | - | 6.44 | | MEF2A | MA0052.3 | chr9:93955890-93955902 | TCTATTTTTAGC | - | 6.92 | | MEF2A | MA0052.3 | chr9:93954859-93954871 | TCTATTTTTAGA | - | 7.22 | | MEF2B | MA0660.1 | chr9:93955890-93955902 | TCTATTTTTAGC | - | 6.44 | | MEF2B | MA0660.1 | chr9:93955577-93955589 | GCTATTTTTAGC | - | 6.92 | | MEF2C | MA0497.1 | chr9:93954858-93954873 | GTCTATTTTTAGATC | - | 6.9 | | Mafb | MA0117.2 | chr9:93954777-93954789 | AAATTGCTGACA | + | 6.37 | | NR2C2 | MA0504.1 | chr9:93956220-93956235 | AGGGGTCAGAAGTCA | + | 6.18 | | TBP | MA0108.2 | chr9:93955273-93955288 | CTATAAAAAGGCCCC | + | 6.22 | | ZNF263 | MA0528.1 | chr9:93956835-93956856 | TTCTTTCTCTCTCTCTCCTTC | - | 6.01 |
|
| | Number of super-enhancer constituents: 19 | ID | Coordinate | Tissue/cell |
| SE_24346 | chr9:93954308-93954719 | Colon_Crypt_2 | | SE_24346 | chr9:93955224-93956980 | Colon_Crypt_2 | | SE_25080 | chr9:93954487-93958229 | Colon_Crypt_3 | | SE_26319 | chr9:93953887-93962638 | Duodenum_Smooth_Muscle | | SE_27567 | chr9:93953700-93957026 | Esophagus | | SE_28201 | chr9:93953588-93961571 | Fetal_Intestine | | SE_29279 | chr9:93953698-93962183 | Fetal_Intestine_Large | | SE_32161 | chr9:93953837-93959264 | Gastric | | SE_35319 | chr9:93953586-93962988 | HepG2 | | SE_39461 | chr9:93953161-93957016 | Jurkat | | SE_44449 | chr9:93953709-93961317 | NHDF-Ad | | SE_44911 | chr9:93953704-93960917 | NHLF | | SE_47822 | chr9:93954245-93954760 | Pancreas | | SE_47822 | chr9:93954797-93956767 | Pancreas | | SE_51473 | chr9:93953007-93961399 | Skeletal_Muscle | | SE_52908 | chr9:93953760-93959405 | Small_Intestine | | SE_65791 | chr9:93952890-93959470 | Pancreatic_islets | | SE_66540 | chr9:93953161-93957016 | Jurkat | | SE_67269 | chr9:93952624-93957244 | MM1S |
|
| | 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 |
| GH09I091191 | chr9 | 93953312 | 93962483 |
|
Enhancer Sequence | AGTACCTTAT AAAGAAGGGC TGAGCGCTTC ATGGATTTAC TCAAAACCCA GCGCTCTGGG 60
CTACTATGAC CCCAGCCACC AACAGGTGTT GAGACTCCCC TGAGGCCCCG CCAAAACTGG 120
CTGGGGTTTC CTCTCCACCT CAGTGCCACC CCTGTCTCCA AGCCCATACT CCCAGGCATC 180
TCTCAATCAC TACCTCTACA AGACCCCAGG GTCTGGGTAA TGGGGGCTGG CAGAGCCTGG 240
ACTCATTCCT GCAATGACGT CGGATACCAG CGGCACCCAT TCCCTCTCCA AAGCTCATGT 300
CCACAAGGGC AAACGATAGC ATCCCCCTCC ACCCCGGCAG TAAGCAGCAG CGAGTCTCAC 360
CAATTTGAGA GTCTCTAGAA CAACAGATGG TAATTTGTTG ACACAAAGAT TTAAGGGGAC 420
TCAATTACAG TCCCACTGAA AAAGCTCTCT CTAAAATAAG AAAGTATACA GATTCCTCAG 480
CTCGCAGAAA TTGCTGACAG CTTTGTTTTC AACCCTCCAG GAGTAAAAAG AAGCTGACAA 540
CTTATTTTTG CAGGTTATGC TCATTCAAGT CTATTTTTAG ATCTTGTTCC TAAATAAGTA 600
CACCAGAATA GCATTCAGTT TGAAAATCAC CATCTGTTCA GAGCAATGAG CTTGGCCTCG 660
CTGGGCTGGG TATACCTGGC CCATGGCAAG GTGGCAGTCC CCTTGTGGAC TGAACCGAGG 720
GGGCAGTTTC AGGTCTCCAA GTGGTGTTTG AAGAATGCAC TAAAAACAGT CACAGGCAGT 780
TGGCATTTTA AATGCCCATT AAACAACTAT TAATATATTT TATTTATAAG CTGAGAACCA 840
CACAAAAAAT GCCCTTGGCT TTTTAAAAAG AAGTTCAAAT AATCCCTTGT ATTTAAATAG 900
ATTTCTTATA AAAAGGCGAT CCAGCCTAAG TTTGGTAGTT AAGATAAAAA TTAACCTATG 960
GAAAAGAAAG CCAGCTCAGA ACGCTATAAA AAGGCCCCTT CCCCCCCCCC CTTTCTTCCG 1020
GTGTATGGTG GCCCTCCCCT CCCTCTGCAG CCACTTGGTA GTGACTCACG CTTTTCTTTG 1080
GAAATGCAGT TGCTGCGTGA AACACAACGT GAGAATGGGA ATCTGACATA TGAGTAACCC 1140
GGCCGAGAGG CACCTCTTGG AAATGACACT GGGCCTTGGC TAGAATTACG CACAGGCCCT 1200
GGGAGGGCTG CGGCTCGTAG GCCCGTAGGG GGCAGGGTGA GGGCGGAGGT CCTGGCGCCC 1260
CCAGGCCTGA CCCGCCCGCA CCGCTGGGCT ATTTTTAGCG TCCACTAAAC TTAGCCGACT 1320
CCACCCTCTT GAATAACCCA CATCTTAAAA TGCTATTTTT CTCCAACAGG TCAAAAGAAT 1380
TCTGCGAGTT AGAGCGCAGA TTAAGTTGCT AGCGACGGGC ATTGAAGGTT TTAGAACCGA 1440
GAAAATGAGC CGGTGGCGGG GAGCGCGTCC TCAGCGGCCA GGCCCGGCAC GGGGCTCGGG 1500
CACTCGGGGA CACACGGTGG TCGTCGCTGT GTCTCAGCAG GACCCTGTGC GCTGGAGAGC 1560
TTGGGGCCGC GAGTCGCGCA GCAAGGAGGC TTCTGGCTTC TCTATTTTTA GCCTCTGAAC 1620
GTTTTCCAAA ATAATTACCA AAAGGAAATA CACACGCACA CATGGACCTA ACACACAAAA 1680
CGTCCTTCTG CGGGAAGCCA GCACTAGGAA AGAAAAAAAA AAAAATCCGA AGTGAAATTA 1740
TGACACAGGG TTTTGTAACC CGCGGTGGCG CGCTTCTGAA ACCCGAGCCC GGCAGCGGCT 1800
TCTTATCTGC ACCGCGTTCC AGGAAGCAGC CGGCGTTTCG GCCGCGCAAG GGCAGCCGCC 1860
GCACGTAGGC AGCGTCCCCC AGCCCGGGAC CCGCAGGAAT GCGAGGGGCA AGACAGATCG 1920
CCGGAGGAGC AGGGGTCAGA AGTCAGTGTT TAACCACTCA CTGGCTTTCG GTGAAGCCAG 1980
AATGTTAGCA GCGAGTCGCG GTCGGGGGCC TTGGGGTTGC ACACGCTTGC TCCAAGCACC 2040
GAGGCTCAGC TGAGCACATG CACAACCCTC TCGATGCAGC GGAAAGTCGT GTGGCTTAGG 2100
GCCGCACCCC GAATTTCGCC GCACCCGCCG CTGTGCCATT TACAACCCCC CACCCCGCCA 2160
CTGCTGTCAC GTAGCAATCA AGAGTAAAGG TTATCACAAA GTCTGTTCTT CGAAGGAAAG 2220
AGTTGGAATC AAGGACTTCG GACGGGAGGA AGTTGGTAAG TTACCGCTTC CTCCCTCCTG 2280
TTTTCCTCTC CTTGTTTAAC TTCTCACAAG AACATGTGGC AGCGCTGCAG GTTAACTCAT 2340
CTTACATAAC TTCGGGGCCG TGTCAACTGT TCAGAAGAAA GAAAAACAAG TATTCTCTTC 2400
TGTAGAAGTT GTATTTAGAA ACAGGCTCTG TTGTTTAGGA CAAGTTCACT TGTGTTGCCT 2460
GATCACTTGC AGCAGAAAAT CTTAGAACTG CTCCTCAAGC AACAAAAAGT AGGGGCTCCC 2520
ATTTCCATCT TTCTTTCTTT TCTTTTTCTT TCTCTCTCTC TCCTTCCCTC 2570
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