| Tag | Content |
|---|
EnhancerAtlas ID | HS092-38932 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr9:131928370-131931460 |
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: 5 | Chromosome | Start | End |
| chr9 | 131929981 | 131930820 | | chr9 | 131930838 | 131930916 | | chr9 | 131928479 | 131929000 | | chr9 | 131928582 | 131928795 | | chr9 | 131928947 | 131929843 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I129166 | chr9 | 131928464 | 131931823 |
|
Enhancer Sequence | TGAGACGGAG TTTCACTATG TTGCGCAAGC TGGTCTTAGA CTTCTGGACT CAAGGGATCC 60
TCCAGCCTCG GCCTCCCAAA GTGCTGGGAT TACAGGTGTG AGCCACTACG CCTGGCCTGT 120
TAAGTCATAA TTTTGTTCAA CAGGAGAGTC AGTAGGAAAA CTGTCATGCA TTTTGCAATG 180
AAAAGTTATC TGGGCAGAGC TGACCAGTGC CAATATTGCA GCTCTCATTT ACTGGGCACT 240
CACTGTATGT CAGACTCTGA GCTGTAGCAG CCTTACTGCA CAGGCAGGTG CCCCCATGCA 300
TGTCTTCATT TTGCAGACAA GGGACTGGAG GCTCAGGGAG GTGAAGGAAA GAGCTTATTG 360
TCACCTAGAA AGCAGCAGAG CTGGCCAGGC GTGGTGGCTT ACCCCTGTAA TCCCAGCAGT 420
TTGGGACGCC GAGGCGGGTG GATCACCTGA GGTCGGGAGT TTGAGACCAG CCTGACCAAC 480
ATGCAGAAAC CCCGTCTCTA CTAAAAATAC AAAATTAGCC GGGTGTGGTG GCGCATGCCT 540
GTAATCCCAG CTACTCGGGA CTCAGGAGGC TCAGGCAGTA GAATTGCTTG AACCTGGGAG 600
GCGGAGGTTT CGGTGAGCTG AGATCCTGGG CAACAAGAGC AAAACTGTGT CTCAAAAAAA 660
AAAAAAAGAA AAAAAAAAGC AGCAGAGCAT GGTTTGTCTT GAGCTCTATG TGGCTTTGGA 720
GGCTGAGCTT GGAACTGCCA GCCTGGGCTT TGGACGGGCA CCCTGGGTAG GGGTGGTCCT 780
GGGTAGAGAT GGCCCTGGGA ATCCCTCCGG TGCTTGGCCT TGTGCCTGGT GGTCCACAGT 840
CTCACAGTCA CTCATCTGAT ATTTAACAAC TTACAATGAG GAGTGCTCCA CAAGGAACCC 900
TCACATAGCT TGGGATGCTC TCCCATGTTC CGTCTTTGCT GAGGGTCCCT TGGATGGGTG 960
TGTTTGTGGG GCATAGTCTC TGGGGGAAGA GGGGCAGATC CTGGATTGGT CTGGAGCCCC 1020
AGCTGGCCCC GCACAACTAG GAAAACTGGT TGGGGCGGCT GACTCAGGGT GTGTTTATAC 1080
TGGCGTACTC CCCGCCCCCT CCCTCCCTCA GGCACCCTCC CCTCCCGTCC CTGACCCGGG 1140
AGAGGAAGGA AGTTCCTATA ACGTTCATAG TTGCCACTAG TTCTGCGTGT TGTGCATTGG 1200
GCACGGAGCA GGAAGACCTT CACAGGTTGT AACTGGTCCC AGCTTCCTTT GAGGAGACTG 1260
AGTCTCAGAA AAGTCAGGCT GCTCCCTCGA TCCTACAGGG GCAAAGCTGG GATTGGAATC 1320
CAGCTCTGAC TGATGCCCCG GATGGAACTC TCATCCACTG TGATTAGAAT ACAATCTGAG 1380
CACCTCCTGC TTTTCTTTCT GGCCCCATCT CCTGCCTCTC CCACTTGCCC TCTCTCTCAG 1440
CCAGTTCTAT GAACATGCTA AATTTATTCA TTTTCTTTTT TTTCTCTCTC TCTCCTTTCT 1500
TTTCTTCTTC TTTTTTTTTT TTTTTTTTTT TTGCCGGAGT TTCGTTCTTC TTGCCCTGGC 1560
TAGAGTGCAA TGGTGTGATC TTGGCTCACT GCAACCTCCG CCTCCCGGGT TCAAGCGATT 1620
CTCCTCTGTC AGTCCCCCAA GTGGCTGGGA TTACAGGTGC ACACACCAGC ATGCCCAGCC 1680
AATTTTTGTA TTTTTAGTAG AGACAGGGTT TCGCCATGCT GGCCAGGCTG GTCTCACCCT 1740
GACTTCAGGT GATCTGCTCG CCTTGGCCTC CCAAAGTGCT GGGATTAAGG CGTGGGCCAC 1800
CGCGCCTGGC CTCATGTGTT TAGTCTTCAC CTTTTCCGTT CCTTCTGCCT GGAATGCTCC 1860
TCCACCGTTG TTTGTCCAGC TGCTATGGTA GAGACTTCTA GCGCTCATCC ATGTGTACTC 1920
GCCTTTCCTT CCCAGTTACC CAAGAAAACT GCTTTTCCCA GCCCCCTTGC AGTTAGATGA 1980
GGGCCTGGGA CTCATTCTGG CCAATGTGCT CTGAGTGTGA GTGAGGAGAA TCACTTCCAG 2040
GCTGAGGCCA TGAAGAGCCC TTGCAGGACT CCCCAGCTCT CATTCTGTGC CACGGTGGAG 2100
ATTCTGGAAG CCTTGTGTTG AGATAGACGC AGGCTGAATT GCTGAGTCAC CGTATGGAGG 2160
GCAGCAGCCT AGGAGACCTG GCAGTCTGAC TCAGACTTTG CATGGTCAAG AAACAAATCC 2220
TTTCTACCTG CTGGAGATCT TAAAAGAGAA AGAAATCCTT GTGTTAAATC TTTGAGATGC 2280
AGGGATTAAT TTGTTACTGC AGCATAGCCT GTCGTATACT AATAGAGCTG ATCTGTTCAG 2340
GTGTCAGTTG AAATATCACC TTCTCTGATC AAAATATCTA AACTGGTGCC ACCCCCACCC 2400
CCTCCCCCTC CAACCAGTCC TTTCTTTTTT TTTGAGACTT TTTTTTTTTG AGTCTCGTTC 2460
TGTCATCCAG GCTGGGGTGC AATGGTGCTG TGATCTTGGC TCACTCCAGC AGCTGCTTCC 2520
TAGGTGCAAG TGATTCTCCT GTCTCACTTT CCGAGTAGCT GGGATTACAG GCACGCGCCT 2580
CCACGCTAGG CTAATTTTTG TATGTTTGGT AGAGACGGGG TTTCACCATG TTGGCCAGGC 2640
CGGTCTTAAA CTCCTGGCCT CAACTGATCA GCTCACCTCG GCCTCCCAAA GTGCTGGGAT 2700
TACAGGCATG AGCCACGGGC CCTTACCAAT TTTTCTAGCA CTGTGTTTAT TTTCCTGAAA 2760
CACTTATCTA CTTGTTTGTT GCCTTGTGTA TTGTCTGCAC ACCTCCCCCC ACCACTAGAA 2820
TGTAAGCTCT ATGAGGGGAG GGCCCTTCGT TTGTCTTGTT CATGGCTGCA TCCTTGGTGC 2880
CTAGCACAGT GCCTGGCATA TATAGGTACT CAATAAATAT TTGAATGGGT GAATGTGTGT 2940
ATATTTATTT TTTGAGACAA GGTCTCACTG TCACTAAGGC TGGAGCGCAG TGGTGCAATC 3000
ATGGCTCACT GCAGCCTCGA CCTCCTGGGC TCAAGCCATC CTTTTGCCTC AGCCTCCCAA 3060
GTAGCTGGGA CTACAGGCGG GCACCACCAT 3090
|
