Tag | Content |
---|
EnhancerAtlas ID | HS158-17174 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr14:65191820-65194030 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NOTO | MA0710.1 | chr14:65192365-65192375 | GCTAATTAGC | + | 6.02 | NOTO | MA0710.1 | chr14:65192365-65192375 | GCTAATTAGC | - | 6.02 | RELA | MA0107.1 | chr14:65193442-65193452 | GGGAATTTCC | + | 6.02 | RREB1 | MA0073.1 | chr14:65192090-65192110 | GGGATGGTGGTGGTGGGTGG | - | 6.68 | RREB1 | MA0073.1 | chr14:65192097-65192117 | TGGTGGTGGGTGGGTGGGGT | - | 8.17 |
|
| Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
SE_03251 | chr14:65192192-65193789 | Brain_Angular_Gyrus | SE_03953 | chr14:65190319-65195292 | Brain_Anterior_Caudate | SE_04856 | chr14:65180505-65197762 | Brain_Cingulate_Gyrus | SE_05821 | chr14:65180438-65199821 | Brain_Hippocampus_Middle | SE_06781 | chr14:65180403-65192060 | Brain_Hippocampus_Middle_150 | SE_06781 | chr14:65192065-65195493 | Brain_Hippocampus_Middle_150 | SE_07938 | chr14:65190169-65194504 | Brain_Inferior_Temporal_Lobe | SE_19856 | chr14:65188989-65195748 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20478 | chr14:65185982-65194236 | CD56 | SE_22874 | chr14:65186008-65194196 | CD8_primiary | SE_23289 | chr14:65190472-65194123 | Colon_Crypt_1 | SE_24426 | chr14:65191797-65193408 | Colon_Crypt_2 | SE_24426 | chr14:65193426-65194045 | Colon_Crypt_2 | SE_26750 | chr14:65181719-65194103 | Esophagus | SE_27717 | chr14:65189231-65195032 | Fetal_Intestine | SE_28783 | chr14:65190366-65194949 | Fetal_Intestine_Large | SE_32308 | chr14:65191832-65193491 | Gastric | SE_36148 | chr14:65181584-65194566 | HMEC | SE_47632 | chr14:65192885-65193854 | Pancreas | SE_49272 | chr14:65190395-65192755 | Right_Atrium | SE_50477 | chr14:65190429-65195289 | Sigmoid_Colon | SE_54434 | chr14:65191114-65192192 | Spleen | SE_57093 | chr14:65190453-65193416 | VACO_400 | SE_57093 | chr14:65193490-65194055 | VACO_400 | SE_57603 | chr14:65191845-65193429 | VACO_503 | SE_57603 | chr14:65193483-65194199 | VACO_503 | SE_57932 | chr14:65192783-65193254 | VACO_9m | SE_57932 | chr14:65193561-65193963 | VACO_9m | SE_64475 | chr14:65185799-65194369 | NHEK | SE_65298 | chr14:65181865-65199543 | Pancreatic_islets | SE_68953 | chr14:65192622-65194088 | H9 |
|
| 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 |
GH14I064714 | chr14 | 65180858 | 65194899 |
|
Enhancer Sequence | TGCTTATGTT GCTATCCTCT TACAGTGGGA TCCCCAGAGA GGGACCCTCA AAAGGTCCCT 60 TTTAGAGACA AATCTCCCTA ATGGTGTGTG TGTTGGGGTA GGGGTGGGGC TGTGAGTAAT 120 CTTTTGCTTT AAGACTGTGA ACTGGCTGGC TGTGAAATCC ATTTGGGAGT GGGGCCGTTT 180 CCATTTAGCT TCCCCAGAGA AGCTGACTGA CCCCAGATGT GATCTGGGAA AGGTCTTAGG 240 CTGTAAATCC CTGCCCCTTT GTTCCCTGCT GGGATGGTGG TGGTGGGTGG GTGGGGTGCC 300 TAACTGCAGT GCACTTTGAA GGACATCAGA GTGCCACAGG GCTGGGGGTT AAGGGCTGGG 360 GTGGAGCTTG GGTTTTTATC TGTCAGTGCT GGAATGACAT GGTGTTGCCC TGCCTGCTGG 420 TTCTGTAAAA GGCATAGCTG ATTAATTGTA AAGGCCCTTT TGAGGAGGGA GGAAAAAGCA 480 ACAGCCCTAC AATTCCCAGG GGGCTCTCTT CTGAGCAGCT CAAAGAGCTT TACCAAAATG 540 ATCCTGCTAA TTAGCCCTCT GGGCATTGCA CTGGGCTGCG GAGGGGAGCA CTGGGCTGCC 600 ACTGAGTCCC CATCTGCAAG TTGAGAGGCT CATACAGAGC TCCTTGGAGG TGACCCCCTC 660 CAGTGAGACA CAGTGACAAA GTGCTGTGCT CCAGAGCATC CCGGCCAGGT TAGCGGCAGG 720 TGGTAAGTAG GTCTTGAGGC GCTTGATCTG TACCTCAGTA AAAGCATCAG TTTGTTCACC 780 ATTGTTGTTC ATTTGTTAAA TTGGCCCTTA AGACCCCTGC TTTTTAGTAA CTAATGGTGT 840 AGGGCAGAGG GTCTCAAACT AGTCACACTG TCTCAGGCCA GTGCTACAGT AGGAGAAACC 900 TGGGAGGTAG TAAGAGAACA CAGAAAGAGT TCCCCAGGTT TGGGGGATAT TGGAAGGTTC 960 CTGGAGGGGG CGATGTCTAA TTGGAGACCT AAAGATTGGA TGTAAATTAC ATAGGTTGGG 1020 GGATGGTACT GTATGGGGTG GATGGGGACG AGATAACGCC AAGGCAGAGA GAACATTTGC 1080 AAAAGCCGGA GACCCAGGGG TGTTGGTTTC CAGGTTGAGG CATAGGCACA GAAAACCAGG 1140 GGTCAGTGTC AAGGGTTCCC AGAGTAATGG CAGCTTCTAG ATTCTTCTCC TTGTAGCTCA 1200 AGTCTCTGCC CTTTAGTCAT GTCTGGGGTC TAGTCACTTC TGAGCCCTAG AGCTAGGGGT 1260 AGAAGACTCG GGTCAGTAGG GGTGAGAGGG ATGCCCAGGA ACTTACTGTT TTCCTGTGAA 1320 ATAGCAATGA AATGTGTACT CTGCAAAGTG GCATTGGTGA GCTCTAAGGG GTGGGCATGG 1380 GTGTTGCATG GGTGTCCCTG TCCTTCCCAA AGGCTGCAGC CTGAAGTAGT CTGGCCACTC 1440 CACCCTTCCA TCCCCCGGCT GCTCCAGGTG GGCCTGCCTG TGAGCCACAC CATCTGCTTT 1500 GGGAATAAAG TCCACCTGAG GCTCTGTTTG CCTCACCTGG GTGCAGTTTA CTGCTTTCTC 1560 TGCTGCCCCC GCCCAGCTGT GCCAAGGGGA GCTTACAGAG ACTCACTGAT GGCTTAGCCC 1620 TGGGGAATTT CCTGGGGCCT GGGATGAGTC AGAGGCAGCC TGTACCAGGT GCTGGGGTGG 1680 GGCTGCGGAG TCGGGGGATA ATGCTGGCTC AGCCAGTCAG TATCCAGAAA GTTTCAGGTT 1740 TGTGGTGAAG CCGCCGGTGC CCCTGAGGTT TTGCAGTCTT AGGGAGAATA TTACCCCTGT 1800 TATGTGTCTT GTCTTAACAT TGTAAGAACC AGATCTTTGC CCATCCCTGT ACAGTGACCC 1860 CAGCACAGGC CACAGACAGG GGGGCACTTG GGAAGTTCTT CTTCACAACT GCCATTATTA 1920 TCACCATATT GATGGTGTAT GGAGCACGTA CCCTATGCCA GGCATCATGC TCAGAGCTTT 1980 ACGAACAGCA GGTGGCTTCA TCTGGGAGGA CACAGCCATG GGGTAGGCTG TATCCATCCT 2040 CATTTTACAG GTGAGGAGCT GAGGCTCTGA GGGACTAAGT ACTGTGCCCC AGCAGTGGGG 2100 CTGGGCTGTG AATTCCTTAG AGGGTACCTG GACCACTGTG CTGGCAGGTG GACTTGGGCA 2160 CCCTCATCAG TGCTCATAGA GTCTGAGAAC AGGGCCCTTC TTGGGATTCA 2210
|