| Tag | Content |
|---|
EnhancerAtlas ID | HS047-20378 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr2:219760720-219763640 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr2:219763120-219763139 | CAGCGCCCTCTGTTGGTGA | - | 6.59 | | RFX2 | MA0600.2 | chr2:219761928-219761944 | CGTTACCATGGCAAGG | - | 6 | | RFX5 | MA0510.2 | chr2:219761802-219761818 | GGTTACTGTGGTAACC | + | 6.03 | | RFX5 | MA0510.2 | chr2:219761928-219761944 | CGTTACCATGGCAAGG | - | 6.14 | | RFX5 | MA0510.2 | chr2:219761928-219761944 | CGTTACCATGGCAAGG | + | 6.42 | | RREB1 | MA0073.1 | chr2:219762180-219762200 | CCCCAACCCACGAAACCCCA | + | 6.01 | | Rxra | MA0512.2 | chr2:219761049-219761063 | GGGGTTAAGGGTCA | + | 6.23 | | ZNF263 | MA0528.1 | chr2:219760981-219761002 | GAGGGAAAAGTAGGAGGAGGA | + | 6.02 | | ZNF263 | MA0528.1 | chr2:219761311-219761332 | TCCTCCTCCCCCCACTTCTCA | - | 6.23 | | ZNF263 | MA0528.1 | chr2:219762993-219763014 | TTCTTCGCCCATCCCTCCTCC | - | 6.61 | | ZNF263 | MA0528.1 | chr2:219761302-219761323 | CCCCTTCTCTCCTCCTCCCCC | - | 7.34 |
|
| | Number of super-enhancer constituents: 13 | ID | Coordinate | Tissue/cell |
| SE_11731 | chr2:219755647-219763246 | CD20 | | SE_17229 | chr2:219759906-219763154 | CD4p_CD225int_CD127p_Tmem | | SE_18189 | chr2:219755344-219763688 | CD4p_CD25-_CD45ROp_Memory | | SE_43911 | chr2:219756648-219763261 | MM1S | | SE_57138 | chr2:219756738-219763491 | VACO_400 | | SE_57485 | chr2:219760203-219763014 | VACO_503 | | SE_58102 | chr2:219760196-219762257 | VACO_9m | | SE_58536 | chr2:219735229-219774909 | Ly1 | | SE_59143 | chr2:219735126-219774980 | Ly3 | | SE_60445 | chr2:219735480-219775196 | DHL6 | | SE_61137 | chr2:219735280-219763865 | HBL1 | | SE_62058 | chr2:219735123-219775057 | Toledo | | SE_67268 | chr2:219756648-219763261 | MM1S |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr2 | 219761000 | 219762778 | | chr2 | 219763191 | 219763600 | | chr2 | 219762802 | 219763005 | | chr2 | 219761045 | 219761550 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I218891 | chr2 | 219756342 | 219763398 |
|
Enhancer Sequence | CAAATGGCAC TGAGCTTATG CATGCTGGAT GAAGGGTGTG GCAGGGATCA ATAAACTGAC 60
AGGAAATAGG GGAAATGGGC TGGAATAAAG TGGGAGGGTG CAGTTTAGAT GGGAGGAAGA 120
ACTTGCCAAC AGCCTGGGAA AGATCAGAGG TGAGACTTGG AAATGAGAAC AGAAGGTGGG 180
TAGAGATCAT TCAGAGAAGG AGAGGACCTC CCCTGCCACC AACAACTGTC ACCTGATGGA 240
TGCTAGGTTA CCTCCTTGCA GGAGGGAAAA GTAGGAGGAG GAAGGGCACT AACAGAATGA 300
GGGTGGTGGA CAGATTAGAA GGCAGTGGTG GGGTTAAGGG TCAGGGAGAG GCAGCCAGGC 360
TGGGGTGAGA TCAGAACGCA GGCATCCCGC TTTGCAGTCA CTCAAGGTCC AGGGTAGAGG 420
CACTCAAAGG TAGACTTGGA GTTGTAGGAG TGCCCCGGCC GGTGAGAAAC AAGGTCAGGG 480
TCATCCCGGA GCTCCCCCTA CTTCCCCCAA ATTAATGTGC CCCCAGCTAG CCCCTGGCAG 540
GGGGCCTTCC ACGTTGGAGT GTGGCCAGGC TCTAGTCACA GCCCCCTTCT CTCCTCCTCC 600
CCCCACTTCT CATGTGGTTG CCGGCAGCTG CCTGCGGTCG CCCCAGCCCC TGCCCTCAAG 660
GCACAGGGAC TTTCCAACAG GGGAAAAAAT GACTTAATGA GAGTGAGAGC TGGGGGCGGG 720
AGGGACAGGT CCCTGTAATC ACCGCTCGGC TGTGGGGCCT GCGCTCCTCC GGGCCCTTCC 780
CCGGCTTCCT GCTGCCAGCG CCTCCCTCGG GCTCCGGTTG GGGAGGAGGA CAAGCTGGCG 840
ACTGGGGTAT CCCTTTTCAG GTGCCAGGCT TTCAGGGGCC CCAGATGCTT TTGCTCCCTA 900
GGCTCGCGGT GTATGGAAGC TGGGACATCC CATGATTCCT CTCTGGACCT TGTCCTTGAA 960
GTTAGGGTTG GCGCATAGGA GGTCTCTCCC TGGAGCGGCT AACCCCTGCT GGTGGGTTGG 1020
GAGGTATAGG ATGGTGAGGA AGCCCTTTGC CACTTCGCGG CTGCGCACTT TGGAATGCCC 1080
CCGGTTACTG TGGTAACCAG GGCAGCCGAG GTGTGTCCTC GGGGCTGGGA GGCGCCCGCC 1140
CCCCCACCTT TTCTCGCCGC CCGCGGGGCC AGGCCGGGCC GCTGCGGTGC GCGGGGGTGG 1200
GGGTGTGCCG TTACCATGGC AAGGGTGCGC AAGGAGGGCA CATTCTTCCC CAGGGTGGGA 1260
GCGCCCTGGG GATACAAGAA GGGGGGTAAC CGAGGCAGCA GAAAGGGGAG GGGGGTCAGA 1320
ATGAGGGAGG AGTCTCGGAC TAGACTAACC AGGGCTTCTG GGGTTTGGGT GGGGAGTTTG 1380
GAATCTGCCC CCACCACCCC CGCAGCTCTC CCGAGGCATC CCGCTCCTCC TCCTTTCACC 1440
CTCGCTGGGG TTCAACCTCC CCCCAACCCA CGAAACCCCA GTTTCCGGGG AAGGGATCCC 1500
CGGCTACCTA CCCAAAGGCC TTTGGCTTCC TCCAAAGCCG GGCCTGAAGA GCTAAGGGGC 1560
CCGCTCCCTT CCCCCCAGTG GAGTTGCAGC CCAGACTGCT GGCCAAAGCC CTGCAATTAA 1620
GCCCCTCGCC CGCCCCTGCG CCGCCCGCCC GTCCTCCGCC AGGCCGGGTC TGCGCCGCCA 1680
ATTGCAGCAG CACGCAGCAG CTGATTACCC CTACCGGAGC CTGGGGAGCG GCCAGGGGTG 1740
GGGACAGCGG GCAGGTCAAG GGGGCAGGGT CCCTGGGGTT GTCCCTGGCC CCGGGGTCCT 1800
TCACTGGAGC TTCTGATTCT AGCGCAGCTT CTCCGCCCCA AACAATATGG GGAGAAGGGG 1860
TCTGCTCAGT ACTCCATCCT GCTGTGCCTC AGTTTCTCAC TCCTCCACTG CACACCGCAC 1920
CCAGAGCAGA AAGAGCTCAG AAACGGTCTG TGTGTATGTG TGGATGTTAG AACATCTGGA 1980
GTTAAGGGCT GGATTCTCCA CAAGTTCAAG GCCTTAAAGT CCAGCTCTCT TTCCGGCTGC 2040
AGACTGCCGC GTGGGTCTCT CCTGGCCCTG CGCCCCGCCC TGTGGACCCC TCTCGGTCAT 2100
GCTGAGGCAG CCTAGGGCCG CGGGCAGCCC AGACTGCACT TTGGTGGGTA TCAGAAAACG 2160
TCCCGCCTGG GTGGGAGGCG CCCCTCTTCT GCCCTACAGG GGAAGGCAAT CCGGGAGTCT 2220
GCAGAGCAGC GACAGTGGAG TGCTCTGCCA CCACCCTTGC CCCCTGCCGT CCCTTCTTCG 2280
CCCATCCCTC CTCCGCCTGC GGGTCTGCAG GGGCTCGGGT AGGGCTTCGC GCCTCCCGCG 2340
GTCCAGCTGT CTACATCTGG CCAGCAGCTG GGAGCCGCCC ACCGCGAACT GCTGAGGACA 2400
CAGCGCCCTC TGTTGGTGAG AGGCGGCGGC GCATCAGCTT TCGGGCCTTG GGGCGCGTAG 2460
CCCCAGTTAA TTGGGTGGGT CTCGGGTTCA ACTCATCCGC TGCCCTTTGA CTTGGGAACC 2520
ACCCGCCCTC TGCCTCGCAC GGCGCCCAAA TCCGACTTCA CGGGCCCATT GCTTTCCGCC 2580
GGCCGCGGCC TTGCTGGCCC TCTTTCCTCC GTCCCTGTGT GCTTAAAACC CAGCTCAGCG 2640
ACCTAGCTAG CTGTCCACCA ACCTCCCATT TTTCCAGTTG TCTCAGCTTC GTCCCGCAGG 2700
TTCTGCGGCA CTATCTCTCC GCGCCCAACG TAAAAGTCCT TAAATAGGAA CATGATTACA 2760
TAAGTCACCG CCCATTTGCT CAATGGAATT CCTCGCCGCG TCCTTAAAAA TGAGGCGTTT 2820
GAAATATATT TAGTTCCTGA GACCGTGTTT GCTCTAAATG GATGGGGGGT GGAGGAGAAG 2880
ATGCAAGACA CAAAATAGCA CAAGGCAGGG TCCCTCTTTA 2920
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