Tag | Content |
---|
EnhancerAtlas ID | HS182-21849 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr9:114821990-114824600 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EN2 | MA0642.1 | chr9:114823243-114823253 | CCCAATTAGC | + | 6.02 | KLF5 | MA0599.1 | chr9:114822230-114822240 | GCCCCGCCCC | + | 6.02 | Nr2f6(var.2) | MA0728.1 | chr9:114822763-114822778 | TGAACTCCTGACCTC | - | 6.22 | Stat6 | MA0520.1 | chr9:114822193-114822208 | AGTTCTTTGGAAATG | - | 6.39 | TP53 | MA0106.3 | chr9:114824577-114824595 | GACATGTCCTAACATGCA | - | 6.22 | TP53 | MA0106.3 | chr9:114824577-114824595 | GACATGTCCTAACATGCA | + | 6.24 | TP63 | MA0525.2 | chr9:114824577-114824595 | GACATGTCCTAACATGCA | + | 6.75 | TP63 | MA0525.2 | chr9:114824577-114824595 | GACATGTCCTAACATGCA | - | 7.34 |
|
| Number of super-enhancer constituents: 21 | ID | Coordinate | Tissue/cell |
SE_02843 | chr9:114821302-114822743 | Astrocytes | SE_02843 | chr9:114822752-114824648 | Astrocytes | SE_28204 | chr9:114819961-114824713 | Fetal_Intestine | SE_29159 | chr9:114819796-114824755 | Fetal_Intestine_Large | SE_30746 | chr9:114821264-114822479 | Fetal_Muscle | SE_30746 | chr9:114822664-114824824 | Fetal_Muscle | SE_36599 | chr9:114821040-114824796 | HMEC | SE_37072 | chr9:114820182-114826053 | HSMMtube | SE_38312 | chr9:114820486-114825049 | HUVEC | SE_38966 | chr9:114821262-114824800 | IMR90 | SE_40486 | chr9:114821053-114823986 | K562 | SE_44179 | chr9:114819976-114826304 | NHDF-Ad | SE_44994 | chr9:114821042-114824806 | NHLF | SE_45614 | chr9:114820116-114826322 | Osteoblasts | SE_51720 | chr9:114821228-114824972 | Skeletal_Muscle_Myoblast | SE_55723 | chr9:114821209-114824815 | u87 | SE_58816 | chr9:114652459-114841988 | Ly3 | SE_60959 | chr9:114735912-114841786 | HBL1 | SE_62263 | chr9:114654503-114840084 | Tonsil | SE_63509 | chr9:114821214-114824972 | HSMM | SE_67537 | chr9:114821209-114824815 | u87 |
|
| 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 |
GH09I112057 | chr9 | 114820116 | 114826107 |
|
Enhancer Sequence | TTTGTCCCAT CAAATAGAAA GCCTGGCAGT GAAAGGACGT GTGAGAATAA AAATGCACTG 60 AGAATGAATC ACACTTCCCT TCTATTCCCA TCTATCTGGT ACTTAGCTCC TGCCTCTAGT 120 ACCATGTTGA GCATCTGCTG TCTCTGTCAG GCTTGATAGC AGGGATCTGA ACGACTGACT 180 TGTATTCTTG CAAATCCTTG CACAGTTCTT TGGAAATGAT AGCTCCCCAA CCCCCGCCCT 240 GCCCCGCCCC TCCGCCACCA GCAATGAATG ATTCTTGAGT TGAAATTTCG GAAAAGAGGA 300 AAAGCATACA TCAGCGTGAA ATATAATTAG GGTAATTTCC AAAACTCATT AGGCCATGTA 360 ATTCTATTTT ACCAGTAAAT TTGAACTTCC TGCTTCACAT GTCAAACGCC CTATCTCCTG 420 CTTCCTAAGA GCCCATGAAT CACTAGGTTA AGAAGAGGGA GCCCTCCTCC ACAGTGGGTG 480 TTGGATATGG AAAGTCTCCC CCCACCAGGT TCCCAAACAT CCTAGGTATC CTCAGGGCCC 540 TGATTTTCTT TCTTTTCTTT TCTTTTTTAA GAAGGGAGTC TTGCTCTGCT GCCCAGGCTG 600 GAGTGCAGTG GTGTGATCTC AGCTCACTGC AACCTTTACC TCCCAGGTTC AAGCGATTCT 660 TCTGCTTCAG CCTCCTGAGT AGCCAAGACT ACAGGCACTC GCCACTATGC CCGGTTAATT 720 TTTTTTGTAT TTTTAGTAGA GATGGTGTTC CACCATGTTG GCCAGGCTGG TCTTGAACTC 780 CTGACCTCTT TAGCTGGGGG AAGTTGTTGC ACGTATCACT GCCCTGTGTG CCCACCTCTG 840 CCTCCCAATG GGCTGGGATT ACAGGCGTAA GCCACTGTGC CTGGCCCAGG GTCCTGATTT 900 TCATAAAGTC TTGGCTCACT TTCAGCCAAG GGCTTTCTAC AAAAGAGATA AAGTAAAACC 960 CACAGGGCAA TAAGTTGTCA CCACCAGTAA ACATTTATTA AGCATCCACT GCCTATGGGG 1020 AACACCTGTA ACAACAAACT TGCCGGGAGA CTTGAAGACA TCCCTACATC ATAGCCACAG 1080 GTAAGAAAGT AAATGTTGCA GCACCTCCAT GCGGTCCATA AGTACATCTT TAAATCCCTC 1140 TCATCTTTCC ATGCAGGTGG TGGTGGTCAA GAGCAAGGTC GAGGCTCACC TGTGCCCATT 1200 TGGTTCCGTA CATTGCTCAC TAGAGGCATC ATCGACAGAG TATGAATCAG CTCCCCAATT 1260 AGCCTGACCG TAATCACCTG TGTTGCTTGA TTATTATACA AATTCCCCGA CCTCATACCG 1320 ACCTACTGAA TCGAAATCTC TAGGAGTAGA TTCTGGGAAT CTGTATCGCT GGTAAAGCTC 1380 CCAGGTGATT CCTATAATCT GGCAATGTGG GAGACACGAG CATTAAGGGA ACCCAGCAAC 1440 AGGCTCCATC CTCTGCCTAA CATCAGCAAC CTCAGCAGAG ACTTGGTCCC AGGGACCTTG 1500 CTCCATTATG TACCCCAAGA CACTGTCCCT AAATGGTGCA CAAAGCAGAC TCAGGCCTGT 1560 CTCACACACT GGCAAAGCTG CTGCCCCCCA GCTCAAACCA GGTAGTCAGG CTTAGGAAAA 1620 CCACCCTGCC TGCTGGTAAT TAGCCATGTG ATGTTAAAGA AGCAGCTGTG GCTGTTTGGA 1680 ATATGACTGT TCTGGAAGGA CTTTTCTCCT CTTTTTCACC ACCACACTCC CTCGAATGAC 1740 TCACAGTTCT CCACTTCCTG TTTTGGAGGC GCTGGCCGGC ATATAGCCAC AAGGGTAAGC 1800 TGTCATTTGG CTTTTCTTTT GCATTATGTC ATTATTTGAC ATAAATATCA CATTTGTTCT 1860 TGCAAATGCT CTCAGGAAGT GACATCACAA CTTCTGTTCT CTTTATAATG ACAGAATTAC 1920 AATGCCTTCT GGTAACTTGT CAAGAATCAG AACAATTTAT ACAATGTCCA TCCCTGGAAA 1980 GATCTTTGCA CATTTACTGA ACTTAAATGA ATATAAAAGC AGGAAAACCC TAAGTTTTAT 2040 TATAAATGGA TATACAGATA ATATCGCCAG ACTTTCTTTT TTGTAATTTT ATAATATCTC 2100 ACTTTTTTTT TTTTAACCTT GATTTTACCG AAGGGTCAGC AGAGACAAAG GCAATGTTGG 2160 TGAGGCCATG TACATTTTCA TCTCCTTGAG CTGGTACTGT GAGCAAGCTG TTCATCTCTC 2220 CACGCCAACC TCAATCTTCC TCTCTAAAAA AGGGACTGAT GCTACTTTCC TAATCCTGCC 2280 ATGACCTTTG CAAATAAAAC ACTTAACTGA ACACACTGTA GTCCTCCAAC TGAGGTAAAT 2340 TAATTCCATC CTAATGCCAT CTGGAATCCC AGAAGCAGTC ATTAATTATA CAGTGTCTTG 2400 CCTGTAACTC AATACATGAA AAGACAAAAA GATTTACCTA AATGATCTTT TCAGAAACCA 2460 CTGCACACCC CCCAAGATCA ACCTTACATA AAGGGCAACA TATTCTGCCT TTGGGAAATG 2520 AAACGATGCC CCTGACCCAC CATCCATAAA GGATGTACTA TGAGACATGA GTGCAAAGGA 2580 CAATCCTGAC ATGTCCTAAC ATGCAACCGA 2610
|