Tag | Content |
---|
EnhancerAtlas ID | HS116-10750 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr14:65190480-65193010 |
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 | RREB1 | MA0073.1 | chr14:65192090-65192110 | GGGATGGTGGTGGTGGGTGG | - | 6.68 | RREB1 | MA0073.1 | chr14:65192097-65192117 | TGGTGGTGGGTGGGTGGGGT | - | 8.17 | SOX10 | MA0442.2 | chr14:65191704-65191715 | TGCTTTGTTTT | - | 6.02 |
|
| Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
SE_03251 | chr14:65190497-65192006 | Brain_Angular_Gyrus | 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_08852 | chr14:65191093-65191347 | Brain_Mid_Frontal_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 | chr14:65190542-65191692 | Colon_Crypt_2 | SE_24426 | chr14:65191797-65193408 | 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 | chr14:65191226-65191696 | Gastric | SE_32308 | chr14:65191832-65193491 | Gastric | SE_36148 | chr14:65181584-65194566 | HMEC | SE_49272 | chr14:65190395-65192755 | Right_Atrium | SE_50477 | chr14:65190429-65195289 | Sigmoid_Colon | SE_54434 | chr14:65186992-65191038 | Spleen | SE_54434 | chr14:65191114-65192192 | Spleen | SE_57093 | chr14:65190453-65193416 | VACO_400 | SE_57603 | chr14:65191232-65191706 | VACO_503 | SE_57603 | chr14:65191845-65193429 | VACO_503 | 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: 2 | Chromosome | Start | End |
chr14 | 65190485 | 65190694 | chr14 | 65190716 | 65191649 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH14I064714 | chr14 | 65180858 | 65194899 |
|
Enhancer Sequence | AGTGCTGGGA TTACAGGCGT GAGCCATCAT GCCTGGCCGA GAAAGCGAGT TTTCTAGAAG 60 ACTGATTCAC TGATTGATGA CTGACTGGAT TGATTCATGT TGCAAGATGG AAGAGGTCAT 120 GGCTGGGGCA TACTTAAGAG AACTGGAGAC CCGTATGTGG TAGGATGGGG TAGGCGTGGG 180 TACCTGGTTT GAGGGTTTGG TTGCTGCCTG CCTCATCACC TCCTTCTCTG GCCTCCTACT 240 TCCCTAGCAG ACAGGGTCTT CCGAGATGTG TTTGAAGACC TGAGTTCTCA TCCTGGCTTG 300 GGGGAATCTT ATAGTATGGA GTGGTGCTCT TCAGGTAGGA AGGAAAGGCT GACCCCGCCC 360 GGGGAGCACC AGGGGAGGCA CTTTAACTGT CTCTGTGGGA GTCTGAGCTA CACACACATA 420 ATGGTTCCAA TCCGGTGTCT TAGGGCCAGA ATGCACTCCA GCTGAGTGCA GTGCACTCAG 480 AATGCACTCT GAGAGCGATG CCTCTTATCC GTCACCATCA AACGGTGCCT CCTGACAGTC 540 TGCACTAGTG TCCTGCTTTG TACTCAGTGC CTCATTTGTT CTTCAGCCCT CCCTTTCTTG 600 GGCTCTTGGC TCTTTTCCAG CAAGTCCTCC TGCCCAAGAG AGAGAGAGCC TTGTGATCGT 660 GGGTCTCCTG GTCACTACAG GGCTTCTCTC GTCATCCAAG AAGTTTATAG TCCAATCCTG 720 GTGACCTCAT ACTTTCTCCC TCTTCCTTTC TGCTTACCCA TGACCTGTGA TCCTTTGACC 780 GGGAATCTGT ATTTTACCAT ATTGTTCCAG CCAGAGAATG AATGGCCAAA GGTCACATAG 840 TAGCAGGCCC AAAAACTGCC CTAAGGAATC TTGACTCAGT CCTTCCGAGT GTCATGTCAT 900 AAGCCCCAAT CCTTCAGGTC TTCATATGTC CCCTGCAGCT TATGCTGAAG CAAAGCCATG 960 GCAGCCAGGG CTGTGACCAA TCCTTTGCTT GTGGCCCTGT CTGGTGTGTA GTCCATTAGG 1020 GAGGCAGTGG GCAGGAGAGC ATGAACTCTG GAGCCTCAGT GCCTGAGTTC AAGTCCAGGC 1080 TCTACCACTT ACTACTTCTG TGGCCTCAGT ACCTGCATGT ATAAAATGAG GGTAGTAATA 1140 GAACCTACCT TCTGGAGTTG TTGCAAGGGG TTAGGCACTT TAATATATAC AGAGCGCTCA 1200 GAGCATTTCA GCAGTTGGCT GTTATGCTTT GTTTTAGCCT TAGGAGATAG GAGCTTAGTT 1260 TGCAGACAGG TAGCCTATGA TCAATCAGAG AGAAAACTTC TGTAAGTAGA AAAGACATAT 1320 TAGTTTCTGG GTTTGAAGTG TGCTTATGTT GCTATCCTCT TACAGTGGGA TCCCCAGAGA 1380 GGGACCCTCA AAAGGTCCCT TTTAGAGACA AATCTCCCTA ATGGTGTGTG TGTTGGGGTA 1440 GGGGTGGGGC TGTGAGTAAT CTTTTGCTTT AAGACTGTGA ACTGGCTGGC TGTGAAATCC 1500 ATTTGGGAGT GGGGCCGTTT CCATTTAGCT TCCCCAGAGA AGCTGACTGA CCCCAGATGT 1560 GATCTGGGAA AGGTCTTAGG CTGTAAATCC CTGCCCCTTT GTTCCCTGCT GGGATGGTGG 1620 TGGTGGGTGG GTGGGGTGCC TAACTGCAGT GCACTTTGAA GGACATCAGA GTGCCACAGG 1680 GCTGGGGGTT AAGGGCTGGG GTGGAGCTTG GGTTTTTATC TGTCAGTGCT GGAATGACAT 1740 GGTGTTGCCC TGCCTGCTGG TTCTGTAAAA GGCATAGCTG ATTAATTGTA AAGGCCCTTT 1800 TGAGGAGGGA GGAAAAAGCA ACAGCCCTAC AATTCCCAGG GGGCTCTCTT CTGAGCAGCT 1860 CAAAGAGCTT TACCAAAATG ATCCTGCTAA TTAGCCCTCT GGGCATTGCA CTGGGCTGCG 1920 GAGGGGAGCA CTGGGCTGCC ACTGAGTCCC CATCTGCAAG TTGAGAGGCT CATACAGAGC 1980 TCCTTGGAGG TGACCCCCTC CAGTGAGACA CAGTGACAAA GTGCTGTGCT CCAGAGCATC 2040 CCGGCCAGGT TAGCGGCAGG TGGTAAGTAG GTCTTGAGGC GCTTGATCTG TACCTCAGTA 2100 AAAGCATCAG TTTGTTCACC ATTGTTGTTC ATTTGTTAAA TTGGCCCTTA AGACCCCTGC 2160 TTTTTAGTAA CTAATGGTGT AGGGCAGAGG GTCTCAAACT AGTCACACTG TCTCAGGCCA 2220 GTGCTACAGT AGGAGAAACC TGGGAGGTAG TAAGAGAACA CAGAAAGAGT TCCCCAGGTT 2280 TGGGGGATAT TGGAAGGTTC CTGGAGGGGG CGATGTCTAA TTGGAGACCT AAAGATTGGA 2340 TGTAAATTAC ATAGGTTGGG GGATGGTACT GTATGGGGTG GATGGGGACG AGATAACGCC 2400 AAGGCAGAGA GAACATTTGC AAAAGCCGGA GACCCAGGGG TGTTGGTTTC CAGGTTGAGG 2460 CATAGGCACA GAAAACCAGG GGTCAGTGTC AAGGGTTCCC AGAGTAATGG CAGCTTCTAG 2520 ATTCTTCTCC 2530
|