| Tag | Content |
|---|
EnhancerAtlas ID | HS157-14314 |
Organism | Homo sapiens |
Tissue/cell | PANC-1 |
Coordinate | chr9:131928660-131931410 |
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: 24 | 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 | chr9:131928958-131929830 | 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: 3 | Chromosome | Start | End |
| chr9 | 131929981 | 131930820 | | chr9 | 131930838 | 131930916 | | chr9 | 131928947 | 131929843 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I129166 | chr9 | 131928464 | 131931823 |
|
Enhancer Sequence | CCCCCATGCA TGTCTTCATT TTGCAGACAA GGGACTGGAG GCTCAGGGAG GTGAAGGAAA 60
GAGCTTATTG TCACCTAGAA AGCAGCAGAG CTGGCCAGGC GTGGTGGCTT ACCCCTGTAA 120
TCCCAGCAGT TTGGGACGCC GAGGCGGGTG GATCACCTGA GGTCGGGAGT TTGAGACCAG 180
CCTGACCAAC ATGCAGAAAC CCCGTCTCTA CTAAAAATAC AAAATTAGCC GGGTGTGGTG 240
GCGCATGCCT GTAATCCCAG CTACTCGGGA CTCAGGAGGC TCAGGCAGTA GAATTGCTTG 300
AACCTGGGAG GCGGAGGTTT CGGTGAGCTG AGATCCTGGG CAACAAGAGC AAAACTGTGT 360
CTCAAAAAAA AAAAAAAGAA AAAAAAAAGC AGCAGAGCAT GGTTTGTCTT GAGCTCTATG 420
TGGCTTTGGA GGCTGAGCTT GGAACTGCCA GCCTGGGCTT TGGACGGGCA CCCTGGGTAG 480
GGGTGGTCCT GGGTAGAGAT GGCCCTGGGA ATCCCTCCGG TGCTTGGCCT TGTGCCTGGT 540
GGTCCACAGT CTCACAGTCA CTCATCTGAT ATTTAACAAC TTACAATGAG GAGTGCTCCA 600
CAAGGAACCC TCACATAGCT TGGGATGCTC TCCCATGTTC CGTCTTTGCT GAGGGTCCCT 660
TGGATGGGTG TGTTTGTGGG GCATAGTCTC TGGGGGAAGA GGGGCAGATC CTGGATTGGT 720
CTGGAGCCCC AGCTGGCCCC GCACAACTAG GAAAACTGGT TGGGGCGGCT GACTCAGGGT 780
GTGTTTATAC TGGCGTACTC CCCGCCCCCT CCCTCCCTCA GGCACCCTCC CCTCCCGTCC 840
CTGACCCGGG AGAGGAAGGA AGTTCCTATA ACGTTCATAG TTGCCACTAG TTCTGCGTGT 900
TGTGCATTGG GCACGGAGCA GGAAGACCTT CACAGGTTGT AACTGGTCCC AGCTTCCTTT 960
GAGGAGACTG AGTCTCAGAA AAGTCAGGCT GCTCCCTCGA TCCTACAGGG GCAAAGCTGG 1020
GATTGGAATC CAGCTCTGAC TGATGCCCCG GATGGAACTC TCATCCACTG TGATTAGAAT 1080
ACAATCTGAG CACCTCCTGC TTTTCTTTCT GGCCCCATCT CCTGCCTCTC CCACTTGCCC 1140
TCTCTCTCAG CCAGTTCTAT GAACATGCTA AATTTATTCA TTTTCTTTTT TTTCTCTCTC 1200
TCTCCTTTCT TTTCTTCTTC TTTTTTTTTT TTTTTTTTTT TTGCCGGAGT TTCGTTCTTC 1260
TTGCCCTGGC TAGAGTGCAA TGGTGTGATC TTGGCTCACT GCAACCTCCG CCTCCCGGGT 1320
TCAAGCGATT CTCCTCTGTC AGTCCCCCAA GTGGCTGGGA TTACAGGTGC ACACACCAGC 1380
ATGCCCAGCC AATTTTTGTA TTTTTAGTAG AGACAGGGTT TCGCCATGCT GGCCAGGCTG 1440
GTCTCACCCT GACTTCAGGT GATCTGCTCG CCTTGGCCTC CCAAAGTGCT GGGATTAAGG 1500
CGTGGGCCAC CGCGCCTGGC CTCATGTGTT TAGTCTTCAC CTTTTCCGTT CCTTCTGCCT 1560
GGAATGCTCC TCCACCGTTG TTTGTCCAGC TGCTATGGTA GAGACTTCTA GCGCTCATCC 1620
ATGTGTACTC GCCTTTCCTT CCCAGTTACC CAAGAAAACT GCTTTTCCCA GCCCCCTTGC 1680
AGTTAGATGA GGGCCTGGGA CTCATTCTGG CCAATGTGCT CTGAGTGTGA GTGAGGAGAA 1740
TCACTTCCAG GCTGAGGCCA TGAAGAGCCC TTGCAGGACT CCCCAGCTCT CATTCTGTGC 1800
CACGGTGGAG ATTCTGGAAG CCTTGTGTTG AGATAGACGC AGGCTGAATT GCTGAGTCAC 1860
CGTATGGAGG GCAGCAGCCT AGGAGACCTG GCAGTCTGAC TCAGACTTTG CATGGTCAAG 1920
AAACAAATCC TTTCTACCTG CTGGAGATCT TAAAAGAGAA AGAAATCCTT GTGTTAAATC 1980
TTTGAGATGC AGGGATTAAT TTGTTACTGC AGCATAGCCT GTCGTATACT AATAGAGCTG 2040
ATCTGTTCAG GTGTCAGTTG AAATATCACC TTCTCTGATC AAAATATCTA AACTGGTGCC 2100
ACCCCCACCC CCTCCCCCTC CAACCAGTCC TTTCTTTTTT TTTGAGACTT TTTTTTTTTG 2160
AGTCTCGTTC TGTCATCCAG GCTGGGGTGC AATGGTGCTG TGATCTTGGC TCACTCCAGC 2220
AGCTGCTTCC TAGGTGCAAG TGATTCTCCT GTCTCACTTT CCGAGTAGCT GGGATTACAG 2280
GCACGCGCCT CCACGCTAGG CTAATTTTTG TATGTTTGGT AGAGACGGGG TTTCACCATG 2340
TTGGCCAGGC CGGTCTTAAA CTCCTGGCCT CAACTGATCA GCTCACCTCG GCCTCCCAAA 2400
GTGCTGGGAT TACAGGCATG AGCCACGGGC CCTTACCAAT TTTTCTAGCA CTGTGTTTAT 2460
TTTCCTGAAA CACTTATCTA CTTGTTTGTT GCCTTGTGTA TTGTCTGCAC ACCTCCCCCC 2520
ACCACTAGAA TGTAAGCTCT ATGAGGGGAG GGCCCTTCGT TTGTCTTGTT CATGGCTGCA 2580
TCCTTGGTGC CTAGCACAGT GCCTGGCATA TATAGGTACT CAATAAATAT TTGAATGGGT 2640
GAATGTGTGT ATATTTATTT TTTGAGACAA GGTCTCACTG TCACTAAGGC TGGAGCGCAG 2700
TGGTGCAATC ATGGCTCACT GCAGCCTCGA CCTCCTGGGC TCAAGCCATC 2750
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