| Tag | Content |
|---|
EnhancerAtlas ID | HS047-35061 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr9:131928360-131931420 |
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 | TATTTTTTGT TGAGACGGAG TTTCACTATG TTGCGCAAGC TGGTCTTAGA CTTCTGGACT 60
CAAGGGATCC TCCAGCCTCG GCCTCCCAAA GTGCTGGGAT TACAGGTGTG AGCCACTACG 120
CCTGGCCTGT TAAGTCATAA TTTTGTTCAA CAGGAGAGTC AGTAGGAAAA CTGTCATGCA 180
TTTTGCAATG AAAAGTTATC TGGGCAGAGC TGACCAGTGC CAATATTGCA GCTCTCATTT 240
ACTGGGCACT CACTGTATGT CAGACTCTGA GCTGTAGCAG CCTTACTGCA CAGGCAGGTG 300
CCCCCATGCA TGTCTTCATT TTGCAGACAA GGGACTGGAG GCTCAGGGAG GTGAAGGAAA 360
GAGCTTATTG TCACCTAGAA AGCAGCAGAG CTGGCCAGGC GTGGTGGCTT ACCCCTGTAA 420
TCCCAGCAGT TTGGGACGCC GAGGCGGGTG GATCACCTGA GGTCGGGAGT TTGAGACCAG 480
CCTGACCAAC ATGCAGAAAC CCCGTCTCTA CTAAAAATAC AAAATTAGCC GGGTGTGGTG 540
GCGCATGCCT GTAATCCCAG CTACTCGGGA CTCAGGAGGC TCAGGCAGTA GAATTGCTTG 600
AACCTGGGAG GCGGAGGTTT CGGTGAGCTG AGATCCTGGG CAACAAGAGC AAAACTGTGT 660
CTCAAAAAAA AAAAAAAGAA AAAAAAAAGC AGCAGAGCAT GGTTTGTCTT GAGCTCTATG 720
TGGCTTTGGA GGCTGAGCTT GGAACTGCCA GCCTGGGCTT TGGACGGGCA CCCTGGGTAG 780
GGGTGGTCCT GGGTAGAGAT GGCCCTGGGA ATCCCTCCGG TGCTTGGCCT TGTGCCTGGT 840
GGTCCACAGT CTCACAGTCA CTCATCTGAT ATTTAACAAC TTACAATGAG GAGTGCTCCA 900
CAAGGAACCC TCACATAGCT TGGGATGCTC TCCCATGTTC CGTCTTTGCT GAGGGTCCCT 960
TGGATGGGTG TGTTTGTGGG GCATAGTCTC TGGGGGAAGA GGGGCAGATC CTGGATTGGT 1020
CTGGAGCCCC AGCTGGCCCC GCACAACTAG GAAAACTGGT TGGGGCGGCT GACTCAGGGT 1080
GTGTTTATAC TGGCGTACTC CCCGCCCCCT CCCTCCCTCA GGCACCCTCC CCTCCCGTCC 1140
CTGACCCGGG AGAGGAAGGA AGTTCCTATA ACGTTCATAG TTGCCACTAG TTCTGCGTGT 1200
TGTGCATTGG GCACGGAGCA GGAAGACCTT CACAGGTTGT AACTGGTCCC AGCTTCCTTT 1260
GAGGAGACTG AGTCTCAGAA AAGTCAGGCT GCTCCCTCGA TCCTACAGGG GCAAAGCTGG 1320
GATTGGAATC CAGCTCTGAC TGATGCCCCG GATGGAACTC TCATCCACTG TGATTAGAAT 1380
ACAATCTGAG CACCTCCTGC TTTTCTTTCT GGCCCCATCT CCTGCCTCTC CCACTTGCCC 1440
TCTCTCTCAG CCAGTTCTAT GAACATGCTA AATTTATTCA TTTTCTTTTT TTTCTCTCTC 1500
TCTCCTTTCT TTTCTTCTTC TTTTTTTTTT TTTTTTTTTT TTGCCGGAGT TTCGTTCTTC 1560
TTGCCCTGGC TAGAGTGCAA TGGTGTGATC TTGGCTCACT GCAACCTCCG CCTCCCGGGT 1620
TCAAGCGATT CTCCTCTGTC AGTCCCCCAA GTGGCTGGGA TTACAGGTGC ACACACCAGC 1680
ATGCCCAGCC AATTTTTGTA TTTTTAGTAG AGACAGGGTT TCGCCATGCT GGCCAGGCTG 1740
GTCTCACCCT GACTTCAGGT GATCTGCTCG CCTTGGCCTC CCAAAGTGCT GGGATTAAGG 1800
CGTGGGCCAC CGCGCCTGGC CTCATGTGTT TAGTCTTCAC CTTTTCCGTT CCTTCTGCCT 1860
GGAATGCTCC TCCACCGTTG TTTGTCCAGC TGCTATGGTA GAGACTTCTA GCGCTCATCC 1920
ATGTGTACTC GCCTTTCCTT CCCAGTTACC CAAGAAAACT GCTTTTCCCA GCCCCCTTGC 1980
AGTTAGATGA GGGCCTGGGA CTCATTCTGG CCAATGTGCT CTGAGTGTGA GTGAGGAGAA 2040
TCACTTCCAG GCTGAGGCCA TGAAGAGCCC TTGCAGGACT CCCCAGCTCT CATTCTGTGC 2100
CACGGTGGAG ATTCTGGAAG CCTTGTGTTG AGATAGACGC AGGCTGAATT GCTGAGTCAC 2160
CGTATGGAGG GCAGCAGCCT AGGAGACCTG GCAGTCTGAC TCAGACTTTG CATGGTCAAG 2220
AAACAAATCC TTTCTACCTG CTGGAGATCT TAAAAGAGAA AGAAATCCTT GTGTTAAATC 2280
TTTGAGATGC AGGGATTAAT TTGTTACTGC AGCATAGCCT GTCGTATACT AATAGAGCTG 2340
ATCTGTTCAG GTGTCAGTTG AAATATCACC TTCTCTGATC AAAATATCTA AACTGGTGCC 2400
ACCCCCACCC CCTCCCCCTC CAACCAGTCC TTTCTTTTTT TTTGAGACTT TTTTTTTTTG 2460
AGTCTCGTTC TGTCATCCAG GCTGGGGTGC AATGGTGCTG TGATCTTGGC TCACTCCAGC 2520
AGCTGCTTCC TAGGTGCAAG TGATTCTCCT GTCTCACTTT CCGAGTAGCT GGGATTACAG 2580
GCACGCGCCT CCACGCTAGG CTAATTTTTG TATGTTTGGT AGAGACGGGG TTTCACCATG 2640
TTGGCCAGGC CGGTCTTAAA CTCCTGGCCT CAACTGATCA GCTCACCTCG GCCTCCCAAA 2700
GTGCTGGGAT TACAGGCATG AGCCACGGGC CCTTACCAAT TTTTCTAGCA CTGTGTTTAT 2760
TTTCCTGAAA CACTTATCTA CTTGTTTGTT GCCTTGTGTA TTGTCTGCAC ACCTCCCCCC 2820
ACCACTAGAA TGTAAGCTCT ATGAGGGGAG GGCCCTTCGT TTGTCTTGTT CATGGCTGCA 2880
TCCTTGGTGC CTAGCACAGT GCCTGGCATA TATAGGTACT CAATAAATAT TTGAATGGGT 2940
GAATGTGTGT ATATTTATTT TTTGAGACAA GGTCTCACTG TCACTAAGGC TGGAGCGCAG 3000
TGGTGCAATC ATGGCTCACT GCAGCCTCGA CCTCCTGGGC TCAAGCCATC CTTTTGCCTC 3060
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