| Tag | Content |
|---|
EnhancerAtlas ID | HS156-04176 |
Organism | Homo sapiens |
Tissue/cell | P493-6 |
Coordinate | chr15:65183570-65186300 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Ar | MA0007.3 | chr15:65185134-65185151 | GGGAACACAGCGTGCCT | + | 6.14 | | Ar | MA0007.3 | chr15:65185134-65185151 | GGGAACACAGCGTGCCT | - | 6.18 | | NR2C2 | MA0504.1 | chr15:65185196-65185211 | TGCCCTCTGACCTGC | - | 6.56 | | ZNF263 | MA0528.1 | chr15:65184082-65184103 | TCCTTCCCTGTCCCCTCCCCC | - | 6.09 |
|
| | Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
| SE_00179 | chr15:65184020-65192302 | Adipose_Nuclei | | SE_00949 | chr15:65185012-65191657 | Adrenal_Gland | | SE_04179 | chr15:65184024-65186890 | Brain_Anterior_Caudate | | SE_06037 | chr15:65183266-65190782 | Brain_Hippocampus_Middle | | SE_07417 | chr15:65183823-65188537 | Brain_Hippocampus_Middle_150 | | SE_09222 | chr15:65182907-65191234 | CD14 | | SE_12439 | chr15:65183446-65188936 | CD3 | | SE_13731 | chr15:65184779-65190340 | CD34_Primary_RO01536 | | SE_19509 | chr15:65183157-65189177 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20451 | chr15:65183543-65189374 | CD56 | | SE_25922 | chr15:65183499-65191039 | Duodenum_Smooth_Muscle | | SE_26878 | chr15:65183325-65190494 | Esophagus | | SE_29936 | chr15:65183762-65184608 | Fetal_Muscle | | SE_29936 | chr15:65184729-65188809 | Fetal_Muscle | | SE_31256 | chr15:65183577-65189571 | Fetal_Thymus | | SE_31840 | chr15:65183571-65184653 | Gastric | | SE_31840 | chr15:65184688-65191003 | Gastric | | SE_42313 | chr15:65183256-65191830 | Lung | | SE_43954 | chr15:65183041-65189653 | MM1S | | SE_50230 | chr15:65183230-65191055 | Sigmoid_Colon | | SE_52555 | chr15:65183178-65191028 | Small_Intestine | | SE_53569 | chr15:65182985-65192126 | Spleen | | SE_55484 | chr15:65183811-65189118 | Thymus | | SE_59387 | chr15:65156174-65198203 | Ly3 | | SE_62974 | chr15:65169474-65198305 | Tonsil | | SE_67436 | chr15:65183041-65189653 | MM1S |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr15 | 65183886 | 65184072 | | chr15 | 65184085 | 65185493 | | chr15 | 65185114 | 65185342 | | chr15 | 65183983 | 65184442 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH15I064891 | chr15 | 65183201 | 65190998 |
|
Enhancer Sequence | ACCTGTCCTG GAGTTGACCA AGCCCAGGGG GAAGTGCCTC CTGGTGTCCA GCCTAAGTCC 60
CCTTGCTGCA AAGTCAGTTC CTGCTCTTGT GTTCTGTTCT CAGTGGATGT GGGAATTAGT 120
TAGAGACCCT CCTCAGAGGG GCAGCCTGAT GATATGGAAA GGCTTATAGG ACGCTGGGTT 180
CAATCCTGGC ACTCCCACTG TCTTGCTGTA TGCCCTTGAG TGGGTACTCA ATGCCTCTCT 240
CTAGGTGTGG GTTTGCTCAT CTGTAAAATG AGGAGGCCAG TTTTGACTGT GAACCCAGCC 300
CTCTTCCCCA CTTCCCCTCT CCCATTGCAG ATGGGATGGG TAGAAGGGGC AGGGGCTCCT 360
GCCTTTTCCT ACTGAGCAAC TAATTTGTGT TTCTCCTCTG GTCAAGGATG TGGGAACTGG 420
GAGGGAGCAG GGCAGTGTGG GATGGTGGAG GAGAAGAAGT TGCTGATGAG AGTGGGAGGC 480
TGGCTGCCAC TAAGCCCTTC CCTACTGGAA ACTCCTTCCC TGTCCCCTCC CCCAGACAAC 540
CTCAGGAAAG GGTCTAGGTG TTTCCACAGT GGTCTAGGAA GGGCTAGACC AATGTGGAGT 600
GGACGACATG CCTGGTGTCT CCCTCTGGAG AGTGCACTCT GGATACTAAT CTGAGTCTCC 660
AAAAAGGAGA AAGGGTTAGG GATCATTTGG TCTCACCTTC CCTCCTGCTT TTACAGAAAG 720
GGAACCAGAG AGGTATAGTG ACTTGTTTAT GTCATGCAGT GACTTGACAG CACAGTGGGA 780
CATGAACTTG GAGTCTTGGA TGTGCAGTCC TGATCTTGCT CCCAGCACTG CTCAGGGAAG 840
ACATTCTTCC TGCTCTGCCT TCCCACCTCT CCTCCCAGGC TCCTGTGATC CCCACAGGGA 900
GAGCTAGAGC TTCTATAAAA ACTGCTGTAA TTGATTCTTA ACAGGAAGTG AGGGCTTTTT 960
CACTTTGAGT TGACAACCAC AGCAGCTACA CACACACACA CACACACACA CACACACACA 1020
CACACAAACA CACACACAAA CACAGACATA CAGTTAAGGT TTAAATATCT GTCCCCTCTG 1080
AAACTCATGT TGAAACTTAT TCCCCAATGT GGCAGTAGTG AAAAGTGGGA TCTTCAAGAG 1140
GTGATTGGGC CATGAGGACT CTGCCCTCAT GAATAGATTA ATTCATTCAT GGATTAATGG 1200
ATTAATGGGT TCATGGATTA ATGGGTTATC ACGGGAATTG GACTGTTGGC TTTATAATAA 1260
GAGGAAGAGA GATCTGAGCT AACATGCTCA ACCCCATCAC CATGTGATGC CCTTCAGGGC 1320
CTCAGGACTC CGCAGAGTCC CCACCACCAA GAAGGACCTC ACAAGGTGCA GCCCTTCAAC 1380
CTTGGACTTC TCATTCTCCA GCACTGCAAG AAAGAATTCC TTTTCTTTAT AAATTACCCA 1440
GTTTCAGGTA CTCTGTTACA AATAACAGAA AACCGACTAA GACACACACA CCCCAAGTTT 1500
GTACACAACC ATGTGCACAC ACACAGTCAC TTGCCCATAC TCCTACGCAT TCAGGCACCC 1560
AGCTGGGAAC ACAGCGTGCC TTTCTTTCTA GTGCCACAAG ATACCCATTT ATAGGCTTCC 1620
AGCTTGTGCC CTCTGACCTG CCTTACATTT TGATAGTAGA GGGTGGATTT GAGGGGGAAG 1680
AGCAGAGACC ACAAGACCAG GCAGGGTTTC CTCAGTGGCT GCACTGCAGG GATTCAATGG 1740
GCAGCAAAGG CCCCCACACC CCAGGCTGGG CCTCATGGCT GAGACTCATC AGTCTTGGGC 1800
CTGGAGGGGC TGCTCTCAGT CTAACAGGCC TGACTGACAG GGAAACCACC AATTTGTCAT 1860
TGGGTTCCAA TCCCGAGTAG CTGGGATTAC AGGCGTGCGC CATGACGCCT GGCTAATTTG 1920
TTTTGTATTT TTAGTACAGA TGGGGTTTCA CCATATTCGC CAGGCTGGTC TCAAACTCCT 1980
GACCTCAGGT GATCTGCCCG CCTTGGTCTC CCAAAGTCCT GGGATTACAG CCGTTAGCCA 2040
CCTCACCCGG CCAGACAAAT GTTTGTTGCA TGAATGTCTT GCCCCTCACA TCTGTGTTCC 2100
GTCCAGCCTT CCTCGCCTCT CCTTTTTCTT GGTGCCCTGG CTGTGGCCAC AGTACTTTCC 2160
TAGGAGGAGG CCTATGCAGG CGCGTAAGGA ACTCGGTGAA GGAGTCAGGG CCCCCAACTC 2220
GGCTCTCGCG AGCTTGCTGT GTGACCTCAG GCCAGTCACC TCCCCTCTTC TGGCCTGGGT 2280
TTCCACACCT GCACAATGGG AACAGCAACC TCAGCTGCCT GCCGTCTCTG ACGTGAGGGC 2340
CAAATAAGAA AAGGTGAGAA GCTGGTCGCA AAGCGGTAAA AAAAGCCTTC AGCGCCGAAG 2400
CCGGGGAGGA AGCCGCTGAT GAAGCTATTG CTGAGAAGTG TGAAGCCCCC ACCCGAGGAT 2460
CCGCTTTTGA AGAGGGACCC GGGGAACGCG TAGGGGGAAA CTGCCTTCCT CTTCCCTCAG 2520
TGGAAAGGGC TGTGCTCATG TCACTGTGAA ACGAAGCTAT TTTTATGTAG TACAACTGCG 2580
ATTATGACAG GGCCTCTTCC TGAAGGGGAA GGGTGGGGAG GAGACCTGAG TCATCAGTGG 2640
GGCGGCCGGC CCCACAGGCT GACACAGGCA GCTTGTGGAA ACCAGGCCCC CCGCCCTGCC 2700
TTCCGCAGGT AGAGGCCCCA GAGAGGGGAA 2730
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