Tag | Content |
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EnhancerAtlas ID | HS073-03806 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr13:99128250-99129330 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GATA2 | MA0036.3 | chr13:99128758-99128769 | AAAGATAAGAA | - | 6.62 |
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| Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
SE_09852 | chr13:99127204-99129958 | CD14 | SE_11626 | chr13:99127788-99131320 | CD20 | SE_27318 | chr13:99128314-99129740 | Esophagus | SE_32245 | chr13:99128412-99129433 | Gastric | SE_37511 | chr13:99127619-99131417 | HSMMtube | SE_38638 | chr13:99127244-99131850 | HUVEC | SE_42842 | chr13:99128374-99129392 | Lung | SE_44584 | chr13:99128314-99129766 | NHDF-Ad | SE_45616 | chr13:99127310-99132615 | Osteoblasts | SE_51002 | chr13:99128378-99129502 | Sigmoid_Colon | SE_53242 | chr13:99128377-99129505 | Small_Intestine | SE_65772 | chr13:99126270-99131228 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr13 | 99128347 | 99129314 | chr13 | 99128638 | 99129073 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH13I098475 | chr13 | 99127656 | 99131531 |
|
Enhancer Sequence | CTAATAGTTT GGGATTTGTT ATATAATAGA TATTATATAA TAATAATAAC TATTATATTA 60 TCCCTAAGAT AATAATTACC TCTGAAAGCT TTTATTCTCA GAAACTCAAA ATAATTGTTC 120 CTATTGACTC CTTTATATCC ACAACTATAT CAGATGAAAG GAAGAAATGT CAGGTATCCA 180 CATCTCCATT TAAAAGGAAA GGAAAACCAG GCTAACAAAG GCTCACTTCA AACCAGACGG 240 GAAGCCCCCC CCCGCCCCCT GCAGAGTGGG GCAGTCAGTC ACAAACAGTA ATTCCACAGA 300 TGACAGCAGC AAAGCCACCA GTGCTCCCCG GAACCACAGA AACGGAGCCA GACAGAGGGC 360 AGATGTCTAA TCGATGCAGG TAGGGTTCCC CCAAATCATG GTCCCCCATT CTTGGTTTTC 420 AGACTTGACA GTGAATGTCT TCACAGCCCA CACCCACACA TTTTAGCCAA CAGGAAGATA 480 CAATCTGGGG CCTTTCACTT AGTTTTAAAA AGATAAGAAA TGTGCTTTAA GCCAAAGGGG 540 ATGAAAACTA GGGCGCTCCT CCACAGGAAG CATCCGACTC AGGCGTGCAC ATCTCTGGGA 600 CAGAGCCCGA CAGTCCTTGC GTGCCTCAGC TCCTTCACAT CCTGTTCCAC ATCCGGAAGT 660 ACTTGTGGGG TGCAGTGTGG GGGCAACCGA GACAGCCCTT GTCACCGAAA CCACAGCCTG 720 ACTCATACCT GGCCCTGCTT TCCGGCCCAT GGGTGAGCTG TGCTGCCTTG GCTCGCAGGC 780 CTGCCCTGGT CTACACAGCA ATCCCAGGGT CAGGGCCACT CTCAGAGGTG GCCTCTCCTC 840 ACACACTGGC CTCGCTGGGA CTCTGGCCTG CCTGGCAGCA GACACACCTG GAATCCAGCC 900 ACCCCTGGCC TTCTCCACCC AGGACCCAGG TGCAGAGAAT GCACTTGTCG CTTTTAGTTT 960 GACCGCACAC ATATGCTCAG AGAAGGTCAA AATGCCCATC TCCATCGCCT GCCAGAAATT 1020 GTCCCAAATT CCAATTAAGA TATTGTCCAA AAGTTACCTC AGACTAAGGC ATTACGCCAC 1080
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