Tag | Content |
---|
EnhancerAtlas ID | HS094-39639 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr7:137670590-137673020 |
Target genes | Number: 10 | Name | Ensembl ID |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr7:137671725-137671736 | CTGCAGCTGTT | - | 6.02 | Tcf12 | MA0521.1 | chr7:137671725-137671736 | CTGCAGCTGTT | - | 6.62 |
|
| Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
SE_00066 | chr7:137667589-137682153 | Adipose_Nuclei | SE_01161 | chr7:137670669-137672074 | Adrenal_Gland | SE_01161 | chr7:137672080-137673316 | Adrenal_Gland | SE_01583 | chr7:137670747-137675600 | Aorta | SE_06592 | chr7:137670557-137675748 | Brain_Hippocampus_Middle | SE_25824 | chr7:137667762-137673330 | Duodenum_Smooth_Muscle | SE_27287 | chr7:137670706-137672046 | Esophagus | SE_27287 | chr7:137672164-137673161 | Esophagus | SE_27744 | chr7:137667496-137672283 | Fetal_Intestine | SE_27744 | chr7:137672455-137673445 | Fetal_Intestine | SE_28585 | chr7:137667434-137674722 | Fetal_Intestine_Large | SE_30032 | chr7:137671119-137672415 | Fetal_Muscle | SE_32391 | chr7:137670737-137673270 | Gastric | SE_35591 | chr7:137667788-137673582 | HepG2 | SE_37226 | chr7:137670234-137672408 | HSMMtube | SE_39130 | chr7:137670746-137672605 | IMR90 | SE_44792 | chr7:137670565-137673332 | NHLF | SE_45544 | chr7:137657492-137687859 | Osteoblasts | SE_46995 | chr7:137670989-137671893 | Ovary | SE_46995 | chr7:137672233-137673100 | Ovary | SE_50455 | chr7:137667391-137675519 | Sigmoid_Colon | SE_51841 | chr7:137670769-137672194 | Skeletal_Muscle_Myoblast | SE_52498 | chr7:137664427-137676040 | Small_Intestine | SE_55864 | chr7:137671360-137672913 | u87 | SE_59162 | chr7:137664421-137694313 | Ly3 | SE_61141 | chr7:137663463-137694162 | HBL1 | SE_61912 | chr7:137664409-137678967 | Toledo | SE_63629 | chr7:137670708-137673152 | HSMM |
|
| 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 |
GH07I137974 | chr7 | 137659055 | 137680050 |
|
Enhancer Sequence | GGATTCAGGT AAGAACTGAA GAAATATTTC AGGTCTTTTT CCCTAAATGC CTTTCACAAT 60 TAGGCCACAA TTCAGAGGTC TTATTCTATT TACTCATTTT ATCCATGAGT TCAGAATGCA 120 GCAAAAATTT TCTTCCTAGG CCTCTCAGAA ACTATTGGAG AAAAAAAAAT AGAAGAAAGG 180 AACCGAATAT CCCCCATCTA GCGGCCACAA ACCAGACATA GTGACACTTT ACTTATGTCA 240 TTTATCTTCC TCCACCATGG CCTTGTGAAA CAGTCTCAGA AAGGTGCTCA CAGTAGGGAG 300 AGCCAGAACC AGATTGTAAG CCTAGACTCA TTCATTTGTT CATCCATTCA TTCACCAAAC 360 ATTTTACTGG ACACCTACCA TGCGCACAGC ACTGTTCTGT TAGCTGGAGA TAAACAGCAG 420 TGAATAAAAG AAAGTCTCTG CTTTCACGGT GTTTCCATTT TGTTAGACGA GAAAACAGAC 480 AAGCACACTT ATCAGGGCTT CCCAACAGGT ATGCCGGGGA GTGCCCCAGC TCCATGGGAC 540 TGGGAAGGAG GGCAAGTTGG CAGCAGAGGC TGGAGCGACT GCACCCCTGA GATGGATTCC 600 ACCCACTATG ATTAGGCTCA TCCATTACTT TGACACAAAG CACCATGCAG ATATCATCAT 660 TTTCCATGAC TGCCATGACA GCAGGGCTCG GGGATACTAA AGAAATCATT TGCCAGTGGT 720 GATAAGGGCT ATGAAGTTGT GCTGACCGCA AAATCCCTGC TCCTCCTACC AACTGCCTTT 780 TCCAGTGGTT GAGCAATCTG CAGACAAGAG GACAGTCAGA ATCCCACACC GAAACTGGGA 840 GGGTGGGAAT AAGAAGCTGA AACTTCCTCA TGCTCCATCT ACCCAGCCAT CCCACCCTCA 900 TTTCAGTGTC CTCCTAGAAG TCTGTATTTC AGTCAAAAGG AAACACTGGA TTTCGACGTG 960 CCTCATGTTC CTCAGCTTGT AAACACAGCT GAGAAACCAA ATGGTTTTTT GGCAGCTACG 1020 TTTCTGCCCC TCTCTTAGCA CACAAGAAAA CGTGTCTGTG AAGACTGCCT TAGAACATGA 1080 TGCCTCGAGC CCAAGGGCGA CCCCACTGCA CCATGCAGGT AACATCACAG CTGTGCTGCA 1140 GCTGTTCGCC TGGAGCTGGT TTGGGCCTTG GCCTCCTCAG CCCACTGCCC CAGCTCTCCC 1200 AGCGGCTCCA ACATGGGTCT TGGGCTGCAG GAGAGCCTGG AGAGAAAGCT TGCAAACCCA 1260 GAGTGGAACC AGAAAAACAA TTCCTGGCAG TGCCTCAGAA ATGAATACCA TTCAGGGGTA 1320 GGAAGTAAAA AGTCAAAACT ACAAAGATCG GAGTCAGGTT CTTTGGTTAC AAAAAATATA 1380 TACTGTTTCC TCACTAGATC CCATCTCTTT CCAAAGGATA ACATCTACTG CCTAAGTCAT 1440 CTGTAACTGG AAAGAGGGAG GGAAATGCCG CACCACAGTT TGACTTTTTA ATGGTACTGA 1500 AATCTATAGG TCTGTGCCTA GTCGTTTGAA TAAGTTTTCA GTAGCAAAAA AAAACAAAAA 1560 ACAAAAAACA GGATACAGTC TTCGGTGTTC AAGGCTTTTG TGGCCAATCT GGCTTCTTGC 1620 TGGACTACAA AGGGAGGCTT ATCTGTGACT AATCTCTAAA AATTAAGTTT AAATCAAAAG 1680 CTGCCACAGG TGACCCCAGC TTATGACTCC ATATGCCAAA AGTCTGTAAT AGCAGGATGC 1740 TGATGGTGGG ACAGGTTTTG TGTGTTGGGG AGACAAGAGA TACACGGGAG CTTTTTGTAT 1800 TTCTGCTCAA TTTTGCTGTG AACATAAAAC TGCTCTAAAA TGCTTTCTGT TTTTGGAGAG 1860 ACAGGATCTG GCTCTGTTGC CCAGAGTGGC GCACAGTGGC ACAATCATGG CTCACTGCAG 1920 CCTCAACCTC CTGGGCTCAG GCGATCCTCC CACCCCGGCC TCCTGCAAGT AGCTGGGACT 1980 ATAGACATAA GCCACCACAC CTTTCTCTAC CTTTTTTAAA AGTTTGTAAC ACGGGTGGTT 2040 CAAACTCACA AGACATTTTC TTACTGACAT AATGTGATAA AAAGTCATCT GTTTCCCAGT 2100 CAGGCCTCAG AAACCCATTT AATTCACCAC ACAGCTAAAC TGTGGAGTGA ATCCTAAACT 2160 CTGTGTCTCC TTCAAAGAGC CTGCTCTGCT CTGGGCTGTG AAGGGTGGCC CTTTCCTCCC 2220 TGTGCAGTCT GAGGCAGAAT TCTCCTTCCT CTGCACCCAC CTCTGTCCTC AGTACTCACA 2280 TGCCCGACCT CAGGCCCAGC TGAAGGGCTT CCTCCTCCCA CACCTGTTCC TCATGTCCCT 2340 GACAGGCCTG AGGGCCATGA CAGGAACAGA GATTCAGTGA AACAGAGAGC AAGGGCAGAA 2400 CCCAGAATCC AGCCACGGCA CGTGGGAGGC 2430
|