Tag | Content |
---|
EnhancerAtlas ID | HS050-28046 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr17:17733970-17736500 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr17:17736236-17736248 | AAACAAACAAAC | - | 6.32 | NR2C2 | MA0504.1 | chr17:17734081-17734096 | TGACCTCTCACCCCT | - | 7.11 | RARA(var.2) | MA0730.1 | chr17:17735322-17735339 | TGACCCCTCTGTGACCC | - | 6.56 | SOX10 | MA0442.2 | chr17:17736257-17736268 | AAAACAAAGAA | + | 6.62 | STAT3 | MA0144.2 | chr17:17734756-17734767 | TTTCTGGGAAG | + | 6.02 | Zfx | MA0146.2 | chr17:17735994-17736008 | GAGGCCGAGGCGGG | - | 6.01 |
|
| Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
SE_00881 | chr17:17733709-17736055 | Adrenal_Gland | SE_03206 | chr17:17734153-17735363 | Brain_Angular_Gyrus | SE_23173 | chr17:17733254-17735884 | Colon_Crypt_1 | SE_23799 | chr17:17733760-17734475 | Colon_Crypt_2 | SE_23799 | chr17:17734505-17734839 | Colon_Crypt_2 | SE_24725 | chr17:17733591-17735526 | Colon_Crypt_3 | SE_26625 | chr17:17734078-17735937 | Esophagus | SE_27885 | chr17:17733606-17735670 | Fetal_Intestine | SE_28899 | chr17:17733505-17735994 | Fetal_Intestine_Large | SE_31441 | chr17:17732630-17735538 | Gastric | SE_31441 | chr17:17735560-17736033 | Gastric | SE_34262 | chr17:17732622-17736139 | HCT-116 | SE_42125 | chr17:17733834-17736003 | Lung | SE_48150 | chr17:17733490-17736067 | Psoas_Muscle | SE_50203 | chr17:17733573-17735794 | Sigmoid_Colon | SE_51164 | chr17:17733014-17735923 | Skeletal_Muscle | SE_52449 | chr17:17733481-17735613 | Small_Intestine | SE_54926 | chr17:17733681-17736164 | Stomach_Smooth_Muscle | SE_57042 | chr17:17733954-17734505 | VACO_400 | SE_60863 | chr17:17723038-17753684 | DHL6 | SE_61850 | chr17:17725940-17761172 | Toledo | SE_62888 | chr17:17723024-17755643 | Tonsil | SE_63332 | chr17:17727040-17744985 | NCI-H82 |
|
| 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 |
GH17I017829 | chr17 | 17732748 | 17735882 |
|
Enhancer Sequence | GGGGTAGGCC ACAAATTCCC CCTAGGGGGA TGGACCCCCA GCCCCGTCCC ACCTCCCACA 60 AGCCCCAACC CAGCAGGGGA CCCACACCTG GAGCCAGTCT CAATGGCTCC CTGACCTCTC 120 ACCCCTGAGC CAGTTAAGGC TTTCCCCACC TCACCCCCGA CACACACAGC CGCCCCTGTG 180 GAGCACATGG TGCAGGCTGT CACACACTGT CAGTGCCCAG GGTCAAAAGG CATGTCCACA 240 TGGCCCGTGG CTGCTAGGAG ACAAGGTCAG AGGCACTTCC TCTGGCCGGC CTGGGCTCCA 300 CCTGTCAGCA GGCAAAGTCC AGATCCCAGG CCTCTGCTGG CAGTGACTCC TGCCTGGAGC 360 TGACCGGGTC ACTCAGGATG TTTGTGTCCA GCTAGGTGAA TGTTGGGCAG AAGGTAACTC 420 CCAACCCGGC TGAGACAAGG GAACTTTATC TTGGAGCACT AGGGAGCCAT GAATGGTTGG 480 AGACCAGGGG AGTTCTGTGC TGTAAGCTAG GGCAGTAACT AGTCTAGAGC TGTGTTTTCT 540 AAGGAGTGCC AGTGCTTGGT GGAACTAGGG AGAGAACTGG GGCATGAGAT ATCCTGGGGA 600 GAGGTATGGG GTGGCAGAGC GGGCCCCCAT TGTGCCCTAC CAGGGCTGGC CTGGACCCAG 660 CAAACAGCCA GACACATGAC TAGAAGCAAG GCCCTGTTGT GGCTGGGCTG GGCATGCTGG 720 GAGGGACATC AGGGCGGGAG AACTCTGAGA ACGCACTGCT CGGGGCAAGG TGACACCCAG 780 AAGGGCTTTC TGGGAAGCAG CCTCTGACGG GGCTTGGCAG ACATCTGGGG TCCGACAGAC 840 AAAGAGCAGA CATGACGGGG TCCAGGCATA GGAAAGAGAC CCCGAGGCCC TGTTCCAGGC 900 TCTTGGCCAG AACTCTGTTT CCGTCTGCCT CTTCTGCACT CATAAGCTTG TGCAAAATTG 960 GATAAATTAA TCCTCAGCAG GGAGGTGAAG ACTGCCACGG GCTTAACAAT AATCCCCAAC 1020 ACAGGTACAG GGCCATCTCC TGATCCATCC TCCCCCGACA GCTGCAAGGT ACTCTGAGGC 1080 CCAGAAGGAG ACAGGCTCAC CTGAGGTCTT GGTGCAGATG CAGGACTCAA ACCCAGGGAC 1140 ACTATAGCCA GGGCAGTGCC TTCACCCACA GATGCAAGGA CTCATGGAGG CAGCTCCATC 1200 CCCAAATCCA TTCACATGAC AAGAGTTTGG CTGTGGCAGG CAGCAGGACC GGATGGGGCC 1260 CAAGGCCCTT GGCTGGCTCA CCAGGGCTGG TTCCCAGTCT AATGACTCAA ACACTGCTCT 1320 GGACTGGGAT GGGGAGGTAG CCACATAGCC TCTGACCCCT CTGTGACCCA CTTCCAGGCC 1380 CCCAGAGTAG CCCCTGTGGA GGAGCCTCCC TCAACCCCTC ATCCCCATTC TTAGGAGCCC 1440 AGTGCTTAAG AGCTTAAGAG CTAGGCTCTG GAGCCCACAG CCTGGGTTTG AATTCTGGCT 1500 TTGCCATCAT CTGGCTGTGT GATCTCAGGC AAATCACTTA ACCTCTCTGG TCCTCAAGGC 1560 CGTCATCTTC ATCATATGTC TACCTACTTG GGGTTGTCAG GGGATTAAGT GGGATTATCA 1620 ACACACTGTC TGAAACACAG TAAGTACTCA ATTAGTGTTT TCTGTTCACA TTACGATCCT 1680 CCATCCAAGC AGCCAGAGGG AACTGAAGCT CGGTGTGCCC CTGCTCTGAC CCCCGACTGT 1740 CCTCACATCT AGCCCAGCTC TGCACTCTGG CACTCAAGGC CAGCCTGGCC CCCTCTTATC 1800 CCTCATGTCT CTCAAGGGAC CTGGCATTTC CACCCCCAAA TCTTCAGACC TTATCAAACC 1860 TGCTCAGCTC CACTCCTGGT AGAAGAAGCT TCAAAAGCAG GCTCGACCTC TGACCAGCAA 1920 TTCCCCTCCC AGAACCTCAT CCTAGGAACA CAGTGAGGAT CCGGGCAAAG ACTGGCCTCA 1980 GTGGCCAGGC ACAGTGGCTC ACGCCTGTAA TCCCAGCACT TTGGGAGGCC GAGGCGGGCA 2040 GATCATGAGG TCAGGAGATC GAGACCATCC TGGCTAACAC GGTGAAACCC CGTCTCTACT 2100 AAAAATACAA AAAATTAGCC AGGCATGGTG GCACGCACCT ATAGTCCCAA GCTACTCGGG 2160 AGGCTGAGGC AGGAGAATGG TGTGAACCCG GGAGGCGGAG TTTGCAGTGA GCCGAGATCG 2220 CGCCACTGCA CTCCAGCCTG GGTGACAGAG CAAGACTCTG TCTCAAAAAC AAACAAACAA 2280 AAAAAAAAAA ACAAAGAAAA AAACCGGCCT CAGTGTCCAC TGCAGCAGTT TATAAAGATA 2340 AAACAACCTA GGTGTCCATC GACAGGGAAT CAGGTGGGTA ATAAGAGGAA ACCTTACTGT 2400 CGTCTGGCTG TTGACATGGA ACCAAGCAGA TTCCAATCAG CTGTGAACCA ATGGACCCTA 2460 TTTTAATTTA TAAAAATACA GATCCAGCCG GGCGCGGTGG CTCACGCCTG TAATTCCAGA 2520 ACGTTGGGAG 2530
|