| Tag | Content |
|---|
EnhancerAtlas ID | HS044-12104 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr7:55152580-55155820 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr7:55155597-55155608 | CATGAGTCACT | - | 6.14 | | GATA2 | MA0036.3 | chr7:55153198-55153209 | TTCTTATCTCT | + | 6.32 | | Gata1 | MA0035.3 | chr7:55153198-55153209 | TTCTTATCTCT | + | 6.32 | | POU2F2 | MA0507.1 | chr7:55153043-55153056 | ATCATTTGCATGT | + | 6.1 |
|
| | Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
| SE_00102 | chr7:55153143-55157620 | Adipose_Nuclei | | SE_01411 | chr7:55153534-55155140 | Adrenal_Gland | | SE_02284 | chr7:55152366-55155764 | Astrocytes | | SE_26347 | chr7:55153389-55156011 | Duodenum_Smooth_Muscle | | SE_26554 | chr7:55153313-55156108 | Esophagus | | SE_28434 | chr7:55153998-55156738 | Fetal_Intestine | | SE_29348 | chr7:55154009-55155469 | Fetal_Intestine_Large | | SE_29740 | chr7:55153179-55155277 | Fetal_Muscle | | SE_31784 | chr7:55153520-55155065 | Gastric | | SE_31784 | chr7:55155246-55155703 | Gastric | | SE_35827 | chr7:55153280-55155349 | HMEC | | SE_39226 | chr7:55152899-55155908 | IMR90 | | SE_42526 | chr7:55152348-55156321 | Lung | | SE_44352 | chr7:55152627-55155980 | NHDF-Ad | | SE_44756 | chr7:55152701-55155912 | NHLF | | SE_45557 | chr7:55148460-55156831 | Osteoblasts | | SE_46956 | chr7:55154231-55154621 | Ovary | | SE_47162 | chr7:55151620-55156065 | Panc1 | | SE_48241 | chr7:55153527-55156156 | Psoas_Muscle | | SE_51484 | chr7:55153366-55154856 | Skeletal_Muscle | | SE_51977 | chr7:55153233-55155583 | Skeletal_Muscle_Myoblast | | SE_54760 | chr7:55152837-55156253 | Stomach_Smooth_Muscle | | SE_56293 | chr7:55153271-55155535 | u87 | | SE_63762 | chr7:55153162-55155765 | HSMM | | SE_64220 | chr7:55152906-55154925 | NHEK |
|
| | 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 |
| GH07I055080 | chr7 | 55148541 | 55156580 |
|
Enhancer Sequence | GTCTTCTGTC CAGGTTCTCG GTAGCAGGGC AGTACAGCCC CATCCGTGAT CTTCCATAGT 60
CAGGCATATT GTCACACTCA GTGAGCGGAG AGTCAACCGG GAGGAAGGCA CAGTTTCTCT 120
GGAATGACCT ACGGAATGGT ACGCTCAAAT GCAAATTCTC CTTCCCTTCC CCAGTCCTTG 180
TCCTTCAGAT GGTAATTTAG GAGCTGAAGG TCAGGGCACC AGCAGCCTTT GGAAGCCTAC 240
AGGACAACAG TCAGCCTGGC TAGAAAAAAA AACAATGTCA CAGGCATGTT GTGTTTAATC 300
ACATGAAGGA TATTTGCATT GTTTTCCAAC TGATGCCAGC AGACACATTG TCAGTGGTAT 360
CATGCCTGGG GTATCAGAGT TGACATTGGG TTGCCCCTTC TCTGAGGCAT TCATGTAAAT 420
CCTTTTAAGT TTATAAAACC TCCATGTGGC TCCTGCATGC TTCATCATTT GCATGTGTCT 480
CTTTTTCCAG GGGAGGCAGC ATGGGGAGCA GGATGCTGGT GGGCTCCAGG TGCAGAGAGC 540
AGGGTGGGCG TCAGACCCCA GGTCCACTGT GCACGCCCTC TTGTAGAGCC CGTTCCGTTG 600
TCCATGAGAT GAGGAGTGTT CTTATCTCTA AAGTATTATC ATGAAAACCT AACAATGTAG 660
AAAGACTAAA GCACATGGGT GGTGCTTCAT AAATAGTATT TCTCCCACTT TCTGAAAACT 720
CCTGCTGAAG TAACTGCACA AGAATCCTTG AACATTTAGA ATTCTGGTTT TAGCCATACC 780
ATAAAGTCAG TAGTGCGTGG TGGAATTCTG CTAACGAAAA TTGCGAAGGA TCAAGGCAGA 840
GTACAGAGCT GGTGTGTAGC GGGTACCTTC TGTCTGCTGG CACTAGGTAT TTTACACATT 900
AAATCAGCTC GTTCTCACAT CAGCTCTTTT AAAAATAAGG AAATGAGGAG CCACAGTGGC 960
CCAACTGATG CAGTGGCAGA AGTAGAATTT GAGCTTGTGC AGATGTGCCT CCGTGTTTTG 1020
TCTCCTGAGC ATGCTGCCCC AAGTTTGACA ATACCAAGAT TTGTACTGGA ACATTCCCTC 1080
CCATCCCCAC CCCCTAGAAG CCCCTCTTCC TCCCTTAGAT TTGACACATA GTTTGAAACC 1140
ACTATTAACT ACCTTATGAG AGCCACTGTT TGTGAAGTGC TGACTATGTG CCAGGTCCCG 1200
TGCCGTGCAA TTTTTGTGAA TTATCTCGTG TCTACAGTGC CTCACAATTT CTCTGCTCAA 1260
TACCTCCATG TTACTGCCGA GGAAAGGGAA GCTCAGAGAG AGTAAGTAAT TTGCTCGAGT 1320
TAAAGAGCTG GCCAGGACAG CCAGGGGCTT GCACCCCGGA GCCTTCATCC ACTACACTGT 1380
CAGCTGGTAT CTCAACCAGC CATTACAGGC TGTAAAAAAA TTATATAAGA TAGTCTATGG 1440
TAATGCAGAA AAGTGAGGTT ATTTTGCTCC CTTTCCCTTT GAAGAAAAAA GCCCTGGAAA 1500
GACATATCAC TTGAGTATGG GAAAAAATGA AGCTGTGGCT TTTCTGTGAG TCAATTCTTT 1560
CCTGGCAGCT TCTTGGAATA AGACCAAGTA TAGCAGCAGA GTTTTCTGTT TTAATTTGAG 1620
CTGCAGGGTG ACTTTTTTTC TTCTATGCTT TCATCTCTCT GTGGCTTCTT TTGCCTCGTT 1680
AATTTCATGC CCTGCCCAGG CGGGCTACTG TGCTGCCCAG TCACCCGGGT CTGGGGCGGC 1740
CACCGCTGGC CAGCAGGCAG GCCCTCCAGA GGCAGAGGTG GCCACGCTTA GGTCGCTCCC 1800
GCTGTGGAGG CGGCACACTT GGGTGGCAGC ACAGCTGTGA TGTGGCGGCA GCTGGCAGCC 1860
CCATGGGAAA GATGTGTGAA GTGTGGGGTT TGACGACCCA TGGGAGAACA GACTTTCTTC 1920
CTCTTCTTGT TTTCCCTTCA AAGCCGTGAG TCAACCTCAA ATTCTCTGTC TTTTTTCTCC 1980
ACCCCCTCGT GCCTCTCTCC CTCACGCTCT GCATCTCTCA TTGCAAGCTT GCATTTTTTT 2040
GCACACAACA CTATCTTAAT ATTTCTCTTT TCTGCAGGCA GGAAATGAGA AGTCATTTTT 2100
CAGGGTCATT CAGGAAGTCA TCCAGAGTTA TAATGGCCCA TTATCTACTG GTCAGAGTTT 2160
ACTTAGGCTT TCACTACTTC CACTGCCCAC TTGAAACAGG GAAAAATATT TTCCCCCCGC 2220
GCTGTGAGTG TGCTATTTAG AGCTGACCAC AAGCGGGGGG AAGAGAGGAT GGCTCGGATG 2280
CTGCATTTCC ACTGAGAACA CAAGGCTGGC AAAGCTTGTC TGCTGCCCAG CAAGCACTTC 2340
AGGCTCACAC CATTTTAGGT TCACTTTAAG TAGTTTCTCA ATTGTTAAAA AAAAAACAAA 2400
AAAAAAAAAA CCTGTACTCT GAGGATATGC TTATAATCCC ATAGCTAACC CAGAATTTCT 2460
TAGAGAACTG ATCAACATCA GCAGTGGCAC TTACTGAAAA TGCACATTCT CAGGCCCTGC 2520
GTAGGGCCTA CTGAGTTAGA ATATTAGAGA GCAGGTCTCA GAAACATTCT ATCCGGCAGT 2580
CTTATTCTAT GCACCCGAAG GGATAAGAGC CATGCTTTCA TGAAACATGG GTTGTGTGTA 2640
AAATGTTTAA AAGGTATGGC AAAATGTGTT TGATTGGCAC CAAGGATTTC TGGTTCCTCC 2700
TAGAATCATT AATCAAACTT TGAAGGAGAA ATAAGAGAGT CGGCATTTTC TTGCACATTC 2760
TTTGTGATGT TGTGATGAGT TGGAAACTTC CCGATTGGGT TTATTAGAGC ATGAACACCC 2820
AGGCACCCAG CTTCTAGCCA GCCCTGTCAG GCAGAGTCTC CTCGAAGATG TGGAAAGGAC 2880
TGACCAACAG CTGAGGCCTA CAGGAACCTG AGCAGGCAAG GGGAGAGGCA CCCCGGAACC 2940
AGGAGCAATG GCCTTCCCAC CCTCCCTCGT CCTCTCCTCT TCTCCTTTTG GAGTTGCAGG 3000
CCACAGAAAG GAAGTGACAT GAGTCACTTT GGGCCTTCTT AATTCCTTCA TCAAAGGCAG 3060
CACAGGTGTG TATGTGTGTT GGTGGCTAAT TGAGGTAGGC CCACAGAGGA GATAACAGAT 3120
GGACATACTA TTTCCTTTCT TCCATTCTGA TATAATTCAG GGTATAAACA CACACACACA 3180
CACACACACA CATTCTCACT TCTTTGGCAT CTACCACACC TGCCCCAGTG CCCATTTCTC 3240
|
