| Tag | Content |
|---|
EnhancerAtlas ID | HS098-10737 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr11:75022440-75023700 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2C | MA0524.2 | chr11:75022753-75022765 | AGCCCCAGGGCA | + | 6.11 | | ZNF263 | MA0528.1 | chr11:75023176-75023197 | CCTCTCCCTTCTCCTTCCTCC | - | 6.86 | | ZNF263 | MA0528.1 | chr11:75023179-75023200 | CTCCCTTCTCCTTCCTCCACC | - | 7.29 |
|
| | Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
| SE_00135 | chr11:75016201-75027347 | Adipose_Nuclei | | SE_03287 | chr11:75022298-75024209 | Brain_Angular_Gyrus | | SE_04031 | chr11:75020093-75025864 | Brain_Anterior_Caudate | | SE_04951 | chr11:75011977-75027109 | Brain_Cingulate_Gyrus | | SE_05927 | chr11:75011975-75026931 | Brain_Hippocampus_Middle | | SE_07122 | chr11:75020120-75026037 | Brain_Hippocampus_Middle_150 | | SE_07907 | chr11:75011958-75027094 | Brain_Inferior_Temporal_Lobe | | SE_13386 | chr11:75022344-75023722 | CD34_Primary_RO01536 | | SE_23271 | chr11:75022374-75023957 | Colon_Crypt_1 | | SE_24003 | chr11:75022650-75023773 | Colon_Crypt_2 | | SE_25192 | chr11:75022381-75023965 | Colon_Crypt_3 | | SE_25898 | chr11:75021122-75025829 | Duodenum_Smooth_Muscle | | SE_26962 | chr11:75022396-75025702 | Esophagus | | SE_28109 | chr11:75022444-75023821 | Fetal_Intestine | | SE_29208 | chr11:75022428-75023853 | Fetal_Intestine_Large | | SE_31429 | chr11:75022250-75025778 | Gastric | | SE_42220 | chr11:75019878-75027219 | Lung | | SE_46889 | chr11:75022715-75023607 | Ovary | | SE_47208 | chr11:75022351-75024084 | Panc1 | | SE_50175 | chr11:75022398-75024164 | Sigmoid_Colon | | SE_52494 | chr11:75022371-75025749 | Small_Intestine | | SE_53599 | chr11:75022306-75025821 | Spleen | | SE_54712 | chr11:75022246-75025882 | Stomach_Smooth_Muscle | | SE_65484 | chr11:75021917-75025888 | Pancreatic_islets |
|
| | 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 |
| GH11I075311 | chr11 | 75022321 | 75025870 |
|
Enhancer Sequence | CCATTCTTTC TGGGATGGGC AGGGGGCTGT TGAGAAAGTT GCAGAGAGCA GGTGACATCT 60
GAGCTGGACT TGAAGCACAA TGAAGAGTTT GTCAGATTGT CAAATTGCAG AAGAGAACGT 120
TAAAGGAACA GGCTATGCAT GGAATGCACA TCCTTACATA GCAGACTGCA CATTTCAAAA 180
ATCAGTTCAA AATCACAATC TCGTTTCACC CTCTCAAATC CCATAATGGT GTTATTAACT 240
GCCTCTCCCA CGGCCCTCCA CCTGCCACAC ACAGGCAAAC AAAAAAAGTA AGGTCCAGTG 300
AAGGCAGATG GTGAGCCCCA GGGCAAACAA ACGGTGACTG ATTTCTGAGT AGAGGGAAGT 360
GAGGGGTGGA CTCTGGCTGA AATGGTCCTC TTCTCACTGA AGTGGGGGAT TCCTGAATTC 420
CTGTCCGGCG GCAGCACCCC ACTTCGGCCC CTGCTGGCCT GTGACACCCT CCTCTCATCC 480
CCAGCATACA CACACACTCC TCCGGCCACC AGGGCCTGTC AGAAGGGGCT GGCTGAGAGG 540
GGACGGCCGG CAGAGGAACC AAGCAGCAGG GCCTGGGCCG AGGGGCTGGG AAAAAGCTGA 600
CCGTTCTCGA AGGCCCAGAT CGGAGGCCCT GCCCAGCCTC TTCCCCTCCT CTAAGTGCTG 660
ATCACCTCAG CCTCTCCCGC TGCAAGTCTC CTTCCATGGC CTCTCCTCTC CCATCTCTTG 720
CAGTGGCTGC TGCTGGCCTC TCCCTTCTCC TTCCTCCACC CTCGCCCTCC CCGGGGAGTG 780
GTGAGCTCAG CCTTTCCCAG CAGCCGTCCC TAGGAATGAT GGGAAATGCA CCGCCAGGAA 840
CTGAGAACAG GCCTGCCCCT GGGAAGGAGT GGGAGAAGAG GCGTCAGGGA CAGGGCTCAA 900
GTCTGCCACT TCCTAGGACC CCTGACCGCC GAAGGGACAG TCTGCCTGTG TGTACTGCAC 960
GCTGGAAGGA CATGGGCTCA GACTGTGTGG ACTGCCAGGG ACCTTGTCTT ACAGATGGGG 1020
AGACAAAGGC CCCAGGAGAG GAGAAAGGGG ACTGACTGCC TGTCCCAGGC ATTGGGAGCC 1080
TTTCATTGTC TCATGTCATC CTCACAACTG CTCTGCAAGG TGTGTGTGGT AGGCTGAGTA 1140
ACAGCCCCCC GAGATGCCCA CATCCTAATC ACCAGAGCTG TGGCTGTGTT GGGTCATGTG 1200
GTAGAAGAGA TTCTGCAGAT GTGATTTTGT TCAGGGCCTT GAGATGGAGA GATTATCCTG 1260
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