| Tag | Content |
|---|
EnhancerAtlas ID | HS162-03466 |
Organism | Homo sapiens |
Tissue/cell | Plasma_cell_myeloma |
Coordinate | chr15:90601090-90603670 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr15:90601201-90601216 | AGGGTACTGTGACCT | - | 6 | | RREB1 | MA0073.1 | chr15:90603329-90603349 | CCCCACCCCACCCCCATACT | + | 6.68 | | RREB1 | MA0073.1 | chr15:90603324-90603344 | CCCCACCCCACCCCACCCCC | + | 7.67 |
|
| | Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
| SE_04139 | chr15:90601915-90602833 | Brain_Anterior_Caudate | | SE_05949 | chr15:90601048-90603242 | Brain_Hippocampus_Middle | | SE_09187 | chr15:90599330-90610815 | CD14 | | SE_23328 | chr15:90601193-90601794 | Colon_Crypt_1 | | SE_23328 | chr15:90602057-90603708 | Colon_Crypt_1 | | SE_23837 | chr15:90601125-90601911 | Colon_Crypt_2 | | SE_23837 | chr15:90602140-90603439 | Colon_Crypt_2 | | SE_26684 | chr15:90600948-90601931 | Esophagus | | SE_26684 | chr15:90601932-90603616 | Esophagus | | SE_27826 | chr15:90600996-90603803 | Fetal_Intestine | | SE_28729 | chr15:90600966-90603950 | Fetal_Intestine_Large | | SE_31431 | chr15:90602097-90603503 | Gastric | | SE_42230 | chr15:90600965-90603597 | Lung | | SE_43613 | chr15:90600736-90603969 | MM1S | | SE_47464 | chr15:90602986-90603355 | Pancreas | | SE_50211 | chr15:90600970-90603901 | Sigmoid_Colon | | SE_52438 | chr15:90600959-90603725 | Small_Intestine | | SE_53426 | chr15:90600949-90609549 | Spleen | | SE_58074 | chr15:90602242-90603541 | VACO_9m | | SE_59156 | chr15:90574114-90608046 | Ly3 | | SE_60018 | chr15:90562472-90609371 | Ly4 | | SE_61051 | chr15:90514694-90642855 | HBL1 | | SE_62744 | chr15:90542925-90609178 | Tonsil | | SE_65318 | chr15:90601118-90601781 | Pancreatic_islets | | SE_65318 | chr15:90602123-90603360 | Pancreatic_islets | | SE_67211 | chr15:90600736-90603969 | MM1S |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr15 | 90602725 | 90603219 | | chr15 | 90601701 | 90601819 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH15I090056 | chr15 | 90599673 | 90609231 |
|
Enhancer Sequence | AACTCTGTGG ACCCAGGGTC TCTGTCTTCA CAAGAGTTTG TGTCTGAGAA GTCACATCAA 60
AATAGTTCAT GCCTCGACAT GGGGGCTTCA CCCCTCATAT CCTTGGGTTT TAGGGTACTG 120
TGACCTCTTA GAGGAGGGAG ATCCTCACAC AGGGGCCACC CTGTGGCAGT CAGACCCACC 180
TCAGCCCTCA GCTTATAGAA GCAGAGGCGT GGCTCCCAGG TCAGGTGTAG GTGCACCCGG 240
GCCTGGGGAA TGGATCAAGA GAGCGAGGGT TGTCAGAGCA GGCCCTGTGG GAGGGGCTCT 300
CTCACCTGGG AGGGCGTCAG GTGAGAAAGC ACTCAGAGCT CCTGGGCCTG AGCTCCTGGG 360
GACTCTGCCA TTAGCAGGGG AAGGCAAGGA AGAAGGCACT TGGGGTGGGG AGGGCCCTCT 420
GGCTTGATTC ACCGGACAAG GTCAGGTCAC TGAGAGTGTG CATCTGCTCT TGCTAACTAA 480
TTTGGAGAGG CCCTTCCCTA TGCTGCCTGG ACACCACCCC AAGGAGGAGG CAGGACTGTC 540
CTGGGAGTGA GGTGCTCAGA GAAGAGCAAA GCCTTGGTAG AACTCTCAGG CAAGAGTTTC 600
ACTCTCCATC TCACTTACCG CATTCAGTCT TGGTCCCTTG GCGACTGTCA GTTTCCTTCT 660
CTTCCCTTTT CTGTACGCTG GTGTCTTTCT CTAGAGACAC TCCCGTGCTG GGCCCCCTCT 720
GTTCCTCTGC AGTCACTGTC CTGTGGGTGG CCTGGCTGTC AGGGGAGATG ATCCACAGTG 780
TGATTATTGT ATCAGTCAGG GTTCTAGAGT AAGAAATAGA ACCAGTAGGA GACACTATAT 840
ATTTATATAT ATATATATAT ACACACATAT ACACACACAC GTACACAGAG AGGTCTCTTT 900
TAAGGAATTG GCTCCTGTGA TTGTGGGGGC TGGCAAGTCC AAAATCTGCA GGGCAGACCC 960
GGGGGCTGGA AACTCAGCAA GATTCATAAG TTACAGTCTC AAGGCAGAAT TCTTTCTCTG 1020
GGAAGCCTCA ATGTTTGCCC TTAAGGCCTT CAACTGATTG ATGCCCACCC ACATTATGGA 1080
GGGTCATCTG CTTTTCTTAA AGTCAACCGA TTGTAAATGT GAGTCACATC TACAGGATAC 1140
CTTCATAGCA ACATCTAGCT TAGCCAAGCA CACAGCCGGG CACCATAGCT TAGCCAAGAT 1200
GACGCATATG ATTTACCACG ACAGTGATGG TCTCAGGCTG AGAGAGGGTC CTCATCCTGT 1260
CCTCATGTAC TTCAAGGGAA GCAGTGCTTG CACTAAATCC TCAAAGATGA TGGGAAATTC 1320
ACCCAGTTCG AGGGAAGGGC AGTCCTGGCA GGGGAATCAG CCTGTGCAGA GGCCCCAAGG 1380
TAGGAAACAT CGGTGAGTTG GGGGCAGAGG GGCAGTGGAG CCTGCCTGGG AGCCATCTTG 1440
GGCAGCAAAT GAAGGCATGG GCAGTGCATC CCGCCTACCA AAAGGCTGTG GGGGCTGCGG 1500
GGCCGGAGAC CTGCATTCTA GCCCTTGCTC CCCCACCGTC TCACTGTGTG ACCTTGGACC 1560
ATTCCCTTCC CCTCCCTGGG CCTCAGTTTC CTCATCTGTT AACAGGGCCG GGTATGGTGC 1620
GCATCACGGG GGTTTGTGGG TTGGTGGCCC TGTGTCAGGG GCCCAGCCAC TCTGACTCCC 1680
AGAGGTGGGG CTCAGTGAAT CTGTCCACAG AGAAAGGGGA AGCAAGGCAG AGACAGGATC 1740
GCAGGAGGAA GAGACTCTCG AACTTCCCCT GCCCCTCCCC CGTGCCGGCG GCAGCTCCCT 1800
GGGCCTCTGG CTCCTGAGGC CTGTGGGCTG GGCAGAAGTG AGACTGTGGC AAGGGGCCCC 1860
GAGGCACAGG CCTTCCAGCT CTCGCTTCCT CTTCCCTTCT GCGCATGTGA GTAGAGTTTC 1920
CCTTGAAGCC TCCTGCGAGG AGGACAACAG GGGAAACCAA GAGGCTGGTT TCCTTAGGCG 1980
GTGAAATCCC GTGCATGTTT TTCACAGCGG GTGTACAGGC CTGGAACTTC CTCTTCTCCT 2040
CCCACCTGGT TACCTGTCCC GCCCACTCCA GCTTCAGCCT CTCCAGCCCC AGGGCCCTGG 2100
ACTCCAAGGG GCAAAAGGCC CAGAGCCACA TCCTGGAGGG CTTGAATGCC AGACCCAGGG 2160
TCAGGAGCCC CCTCCCCGCT CTTGCTCTGT TGGGTCCTGA ACTGCCTCCA CGGAAGCCAG 2220
TCCTCAGTCC CTGTCCCCAC CCCACCCCAC CCCCATACTG CAGCCCCCGC CTCCCAGAGA 2280
TCCGGGTGCT TCATGTGGAC TGAGCTTACG CAAGTCAACT CCCCAAGGGT GAGAACTTTA 2340
ATTTGCCCCT TCTATCTACC CACAAGCAAG CACCTAATAG GTTTAGTAAA TGTGCATTAA 2400
ATCAGTGGCT CAAGCCTGGC ACAGTGGCTT AGGCCTGTCA TCCCAGCACT TTGGGAGGCC 2460
AAGGTGAGAA GATCGCTTGA CCCCAGAAGT TCAAGACCAG CCTGGGCAAC TTAGCAAGAC 2520
TCCACCTCTA CAAAAACAAT GTAAAATTAG ACAGGTGTGG TGGCACATGC CTTTAGTCCC 2580
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