| Tag | Content |
|---|
EnhancerAtlas ID | HS127-32545 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr9:131928480-131931390 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAFK | MA0496.2 | chr9:131930506-131930525 | AATTGCTGAGTCACCGTAT | + | 6.06 | | NFE2L1 | MA0089.2 | chr9:131930507-131930522 | ATTGCTGAGTCACCG | - | 6.97 | | Nfe2l2 | MA0150.2 | chr9:131930509-131930524 | TGCTGAGTCACCGTA | - | 6.68 | | ZNF263 | MA0528.1 | chr9:131930757-131930778 | GCCACCCCCACCCCCTCCCCC | - | 6 |
|
| | Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
| SE_01377 | chr9:131928873-131930959 | Adrenal_Gland | | SE_26914 | chr9:131928223-131931145 | Esophagus | | SE_27869 | chr9:131928909-131930745 | Fetal_Intestine | | SE_28773 | chr9:131928727-131930857 | Fetal_Intestine_Large | | SE_30321 | chr9:131928839-131930038 | Fetal_Muscle | | SE_31776 | chr9:131928375-131931171 | Gastric | | SE_34379 | chr9:131928204-131931924 | HCT-116 | | SE_35053 | chr9:131928605-131931608 | HeLa | | SE_42081 | chr9:131928392-131928852 | LNCaP | | SE_42081 | chr9:131928958-131929830 | LNCaP | | SE_42081 | chr9:131929901-131930683 | LNCaP | | SE_43197 | chr9:131928798-131930727 | Lung | | SE_46983 | chr9:131928949-131929438 | Ovary | | SE_46983 | chr9:131929455-131929836 | Ovary | | SE_46983 | chr9:131930089-131930539 | Ovary | | SE_47992 | chr9:131928939-131929430 | Pancreas | | SE_47992 | chr9:131929486-131929890 | Pancreas | | SE_47992 | chr9:131929957-131930610 | Pancreas | | SE_50677 | chr9:131928813-131930770 | Sigmoid_Colon | | SE_53874 | chr9:131928804-131930748 | Spleen | | SE_56721 | chr9:131928843-131931262 | u87 | | SE_57142 | chr9:131929046-131929865 | VACO_400 | | SE_57142 | chr9:131929927-131930596 | VACO_400 | | SE_57775 | chr9:131928926-131929839 | VACO_503 | | SE_57775 | chr9:131930005-131930538 | VACO_503 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr9 | 131929981 | 131930820 | | chr9 | 131930838 | 131930916 | | chr9 | 131928582 | 131928795 | | chr9 | 131928947 | 131929843 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I129166 | chr9 | 131928464 | 131931823 |
|
Enhancer Sequence | CCTGGCCTGT TAAGTCATAA TTTTGTTCAA CAGGAGAGTC AGTAGGAAAA CTGTCATGCA 60
TTTTGCAATG AAAAGTTATC TGGGCAGAGC TGACCAGTGC CAATATTGCA GCTCTCATTT 120
ACTGGGCACT CACTGTATGT CAGACTCTGA GCTGTAGCAG CCTTACTGCA CAGGCAGGTG 180
CCCCCATGCA TGTCTTCATT TTGCAGACAA GGGACTGGAG GCTCAGGGAG GTGAAGGAAA 240
GAGCTTATTG TCACCTAGAA AGCAGCAGAG CTGGCCAGGC GTGGTGGCTT ACCCCTGTAA 300
TCCCAGCAGT TTGGGACGCC GAGGCGGGTG GATCACCTGA GGTCGGGAGT TTGAGACCAG 360
CCTGACCAAC ATGCAGAAAC CCCGTCTCTA CTAAAAATAC AAAATTAGCC GGGTGTGGTG 420
GCGCATGCCT GTAATCCCAG CTACTCGGGA CTCAGGAGGC TCAGGCAGTA GAATTGCTTG 480
AACCTGGGAG GCGGAGGTTT CGGTGAGCTG AGATCCTGGG CAACAAGAGC AAAACTGTGT 540
CTCAAAAAAA AAAAAAAGAA AAAAAAAAGC AGCAGAGCAT GGTTTGTCTT GAGCTCTATG 600
TGGCTTTGGA GGCTGAGCTT GGAACTGCCA GCCTGGGCTT TGGACGGGCA CCCTGGGTAG 660
GGGTGGTCCT GGGTAGAGAT GGCCCTGGGA ATCCCTCCGG TGCTTGGCCT TGTGCCTGGT 720
GGTCCACAGT CTCACAGTCA CTCATCTGAT ATTTAACAAC TTACAATGAG GAGTGCTCCA 780
CAAGGAACCC TCACATAGCT TGGGATGCTC TCCCATGTTC CGTCTTTGCT GAGGGTCCCT 840
TGGATGGGTG TGTTTGTGGG GCATAGTCTC TGGGGGAAGA GGGGCAGATC CTGGATTGGT 900
CTGGAGCCCC AGCTGGCCCC GCACAACTAG GAAAACTGGT TGGGGCGGCT GACTCAGGGT 960
GTGTTTATAC TGGCGTACTC CCCGCCCCCT CCCTCCCTCA GGCACCCTCC CCTCCCGTCC 1020
CTGACCCGGG AGAGGAAGGA AGTTCCTATA ACGTTCATAG TTGCCACTAG TTCTGCGTGT 1080
TGTGCATTGG GCACGGAGCA GGAAGACCTT CACAGGTTGT AACTGGTCCC AGCTTCCTTT 1140
GAGGAGACTG AGTCTCAGAA AAGTCAGGCT GCTCCCTCGA TCCTACAGGG GCAAAGCTGG 1200
GATTGGAATC CAGCTCTGAC TGATGCCCCG GATGGAACTC TCATCCACTG TGATTAGAAT 1260
ACAATCTGAG CACCTCCTGC TTTTCTTTCT GGCCCCATCT CCTGCCTCTC CCACTTGCCC 1320
TCTCTCTCAG CCAGTTCTAT GAACATGCTA AATTTATTCA TTTTCTTTTT TTTCTCTCTC 1380
TCTCCTTTCT TTTCTTCTTC TTTTTTTTTT TTTTTTTTTT TTGCCGGAGT TTCGTTCTTC 1440
TTGCCCTGGC TAGAGTGCAA TGGTGTGATC TTGGCTCACT GCAACCTCCG CCTCCCGGGT 1500
TCAAGCGATT CTCCTCTGTC AGTCCCCCAA GTGGCTGGGA TTACAGGTGC ACACACCAGC 1560
ATGCCCAGCC AATTTTTGTA TTTTTAGTAG AGACAGGGTT TCGCCATGCT GGCCAGGCTG 1620
GTCTCACCCT GACTTCAGGT GATCTGCTCG CCTTGGCCTC CCAAAGTGCT GGGATTAAGG 1680
CGTGGGCCAC CGCGCCTGGC CTCATGTGTT TAGTCTTCAC CTTTTCCGTT CCTTCTGCCT 1740
GGAATGCTCC TCCACCGTTG TTTGTCCAGC TGCTATGGTA GAGACTTCTA GCGCTCATCC 1800
ATGTGTACTC GCCTTTCCTT CCCAGTTACC CAAGAAAACT GCTTTTCCCA GCCCCCTTGC 1860
AGTTAGATGA GGGCCTGGGA CTCATTCTGG CCAATGTGCT CTGAGTGTGA GTGAGGAGAA 1920
TCACTTCCAG GCTGAGGCCA TGAAGAGCCC TTGCAGGACT CCCCAGCTCT CATTCTGTGC 1980
CACGGTGGAG ATTCTGGAAG CCTTGTGTTG AGATAGACGC AGGCTGAATT GCTGAGTCAC 2040
CGTATGGAGG GCAGCAGCCT AGGAGACCTG GCAGTCTGAC TCAGACTTTG CATGGTCAAG 2100
AAACAAATCC TTTCTACCTG CTGGAGATCT TAAAAGAGAA AGAAATCCTT GTGTTAAATC 2160
TTTGAGATGC AGGGATTAAT TTGTTACTGC AGCATAGCCT GTCGTATACT AATAGAGCTG 2220
ATCTGTTCAG GTGTCAGTTG AAATATCACC TTCTCTGATC AAAATATCTA AACTGGTGCC 2280
ACCCCCACCC CCTCCCCCTC CAACCAGTCC TTTCTTTTTT TTTGAGACTT TTTTTTTTTG 2340
AGTCTCGTTC TGTCATCCAG GCTGGGGTGC AATGGTGCTG TGATCTTGGC TCACTCCAGC 2400
AGCTGCTTCC TAGGTGCAAG TGATTCTCCT GTCTCACTTT CCGAGTAGCT GGGATTACAG 2460
GCACGCGCCT CCACGCTAGG CTAATTTTTG TATGTTTGGT AGAGACGGGG TTTCACCATG 2520
TTGGCCAGGC CGGTCTTAAA CTCCTGGCCT CAACTGATCA GCTCACCTCG GCCTCCCAAA 2580
GTGCTGGGAT TACAGGCATG AGCCACGGGC CCTTACCAAT TTTTCTAGCA CTGTGTTTAT 2640
TTTCCTGAAA CACTTATCTA CTTGTTTGTT GCCTTGTGTA TTGTCTGCAC ACCTCCCCCC 2700
ACCACTAGAA TGTAAGCTCT ATGAGGGGAG GGCCCTTCGT TTGTCTTGTT CATGGCTGCA 2760
TCCTTGGTGC CTAGCACAGT GCCTGGCATA TATAGGTACT CAATAAATAT TTGAATGGGT 2820
GAATGTGTGT ATATTTATTT TTTGAGACAA GGTCTCACTG TCACTAAGGC TGGAGCGCAG 2880
TGGTGCAATC ATGGCTCACT GCAGCCTCGA 2910
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