| Tag | Content |
|---|
EnhancerAtlas ID | HS182-12067 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr2:37842030-37844960 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr2:37843120-37843131 | TGGGTGTGGCT | - | 6.14 | | RFX5 | MA0510.2 | chr2:37843487-37843503 | GGTTGCCTTGGCAATC | + | 6.09 | | RUNX3 | MA0684.1 | chr2:37843984-37843994 | TTTGCGGTTT | - | 6.02 | | ZNF263 | MA0528.1 | chr2:37843614-37843635 | AGAGGAAGGGAGAAGGGAGGA | + | 6.45 | | ZNF263 | MA0528.1 | chr2:37843188-37843209 | GGAGGAGGAAGTGGGTGGAAA | + | 7.06 |
|
| | Number of super-enhancer constituents: 21 | ID | Coordinate | Tissue/cell |
| SE_09261 | chr2:37841016-37844898 | CD14 | | SE_10670 | chr2:37842208-37845652 | CD19_Primary | | SE_11528 | chr2:37841603-37846172 | CD20 | | SE_12153 | chr2:37842058-37844646 | CD3 | | SE_15360 | chr2:37841771-37844475 | CD4_Memory_Primary_7pool | | SE_16522 | chr2:37842422-37844098 | CD4_Naive_Primary_8pool | | SE_17964 | chr2:37841418-37845040 | CD4p_CD25-_CD45ROp_Memory | | SE_18340 | chr2:37841129-37846050 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19132 | chr2:37840835-37845951 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20286 | chr2:37842041-37845410 | CD56 | | SE_21337 | chr2:37841647-37844457 | CD8_Memory_7pool | | SE_22384 | chr2:37841429-37846108 | CD8_primiary | | SE_32540 | chr2:37843020-37845812 | GM12878 | | SE_45823 | chr2:37843058-37844276 | Osteoblasts | | SE_55666 | chr2:37840652-37842707 | u87 | | SE_59201 | chr2:37827295-37865091 | Ly3 | | SE_61134 | chr2:37842214-37883070 | HBL1 | | SE_62438 | chr2:37800533-37911884 | Tonsil | | SE_65823 | chr2:37840967-37842527 | Pancreatic_islets | | SE_65823 | chr2:37842563-37843815 | Pancreatic_islets | | SE_65823 | chr2:37844489-37845661 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr2 | 37843563 | 37844180 | | chr2 | 37842733 | 37843439 | | chr2 | 37844190 | 37844662 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH02I037616 | chr2 | 37841998 | 37842045 | | GH02I037615 | chr2 | 37842167 | 37845500 |
|
Enhancer Sequence | ATCTCCACTT CTTTCTATTG GTTCTGAACA TAGGCCAGTA AGGCAGGAAT GCTTTGTATT 60
GGTCTTTTAA AATTCCAACA ATTTCTTCTG AAGAAAGGGC TCTCCTAGTT TGAAAAATCT 120
TAAGACAATC TGATCTCAGG CCCTGTGGGT GGTTAACAAT ATTTAGGGTC ATAAAAGCTG 180
GTTAACATCA GCAGGCAAGA GATCTTGGAG AAATGAAGGG ACAGAAGTGG AGCAGACAAG 240
GAAAGGGTCA CCCTACCCCA GCAGTCACAG AAGTCACCAA ACTTCACCAA CATGATCTTC 300
CAGCTTGAGC TGCCTCTCCA TGTCCTCTCT CCCCGGCCAG ATCTGATTCA GAGAGTGCCT 360
GGGCCAATGA ACATCTAACT GATATATTGA ACAAATAGAG TTTAATCTGG TATGATCATG 420
AAGTCATGTT TTTCTCATCA CTGCTCCAGC GAATGCCATC TTGGCTCCTT TCTGCTGACT 480
CTTGCCTTTG AATGAAATCT CACAAAGACA TCCTCGTTTT GGTTATTCTT AGACAATAAT 540
GGAAAAGTCC TCTAGTTACA TCTAGCCACA AAAAATATAT ATCTTATTTG AAATTAAAAT 600
GTCCAGGCCC ATGTAATAGT CACATTTAGA GTAGAAACCC TGTTATCCTC CATGCAGGCT 660
GGCTTTCTCC TAGAAACTTG TATGAAGTCA GGGAGGGGAG GCATACCTAC TTTCTGTATT 720
TCTACGGAGC ATGTTTACCA TTCTCCTTTA CTTACTAGGT TGTCTTGGAT GACCCAGGGC 780
TGAGGCAGGG GAACAAGAAG AGATAGGGAA AGTTCTTGCT GGATGGTCTG GTGCTGGTCT 840
CCTCTGGCTA TGGGTCCTTA AGAGGTTCTT TTGCTGGGTC CCACTAACTA CAGCTTCTAG 900
CCTTTTCGGC TGAGGTCACT ATACTATTTC CAGAACGTAC CCCTGAGTGG GGTCACCTTT 960
TAAATGACCC AAGTTGACAG TCCTACTACG AGTTACACAT CTTGGAGTCA CATGCCAGTG 1020
GCCTGGCATT TAAATCAGAG GAGGCTTCAG CTAACATCCT CTTGCGACTA GTGGCAAAGG 1080
GTTGGTGGCC TGGGTGTGGC TGGCTGCTAG AGTGTGGAGC TGGCAGAGGT TTTGCTGGTG 1140
AGATGCTGCC GGGGTTTTGG AGGAGGAAGT GGGTGGAAAT GTGGGCCTTG CCCTCTCTCA 1200
GCCTGTGACA GCCTCTCTCT TTCCTGCTCC TGTTCCTTGC TGTTGGTTGC CCACTTTTCC 1260
CTTGCATCTC TCAGGCCTTG CCTTCTTCTT TGCAGTCACA GCATCCACGT CATCTTTTCC 1320
TTTTTTTATA GGATTTTTGG CTTCATAGAG AGGCTTGGTG GTACCAGCCT CTCTGTTATT 1380
TTTGTTCTAA GCCAGCCACA TCTTCCCCTT TCACTTGCTA GACTGAGAGT ATTCTGGGTG 1440
ACTTTGAATT GAGCAGAGGT TGCCTTGGCA ATCTGTGTAC CCAGGGATAT TGATTGGGAC 1500
TTCAGGAAGT TCATGTGAGC TGACATGCAG ACATAAGAAA GGGTCTACTG GGCAGAAGGA 1560
GCCAGGGCAG GACAGAAGCT ACCAAGAGGA AGGGAGAAGG GAGGAGCTGC CTTAGAGAAA 1620
CACAGGATCT GCCTGCCAGG AGTTCACAGG GTTCAGCAAA TGGCCCAATT GTGATAGACA 1680
AGAATTACAC AGAGGGAGTA AGTTCTAAAG CATTTAAACA TTCCAAGCAA AACAATAAGG 1740
GCTGTGAATA TCGACTCAAT AATCCTTCCT ATTCTAGGAT TTTGGAAAAA CCCATTTTAC 1800
GAATTCCCTA CAAAAAGTTT CCAAATCACT CAGAGAATAG TGTATTTGCC TGAAAAACAT 1860
CCAGACATTC CTTATCAGCA GGCTTATGCT GCCAGCAGTG GTAACACTGT GCTTTCCCCT 1920
AAGATGTGCA AGGTTATGAG CCATGGAACA GATGTTTGCG GTTTATGACT ACCTCTGCTT 1980
AAGCCTGATT TCTTAAACAA GTAGTATCTT TCAGGTGCCT TCTAATATGC ACTGACTGCA 2040
TTTGCTGGAG GCCTCTGTCT TAACACAGTC TCTTAATTCC CCTTCCTTTT GACTGTGTGG 2100
TTCCAGGAAT GCTTGGATTT TAGTAAAATC CTGGCCTTTG ATTAGGGCTG AAACTGTGCC 2160
TACTGCCCTA ATGGTACATG GCAAATTAAA TATCCCCCAA CTTGGGTTTT GATGTGTTTG 2220
CTCTGATGAA CTTTTCTCAT TATGGGTTGA TATGGTTAGG CTTTGTGTCC TCACCCAAAT 2280
CTCATCTTGA ATTGTAATCC CCATAAGCCC CATGTGTCAA GGGAGAGACC AGGTGAAGGT 2340
AACTGAATCA TGCGGGTGGT TTTCCCCATG CGGTTCTCGT GATGGTGAGT GAGTTCTTAC 2400
GAGATCTGAT GGTTTTGTAA GGGACTCTTC CTCCTTTGCT AGGCACTTCT CCTTCTTGCC 2460
ACCTTGTGAA GAAGGTGTCT TGCTTTCTCT TCGCTTTCTA CCATGATTGT AAGTTTCCTG 2520
AAGGCTCCCC AGCCATGCTG AACGGTGAGT CAATTAAACT TCTTTCCTTT ATAAAATTTC 2580
CCAGTCTCGG GCAGTTCTTT ATAGCAGTGT GAGAATGGAA TAATACGTGC ATCGAAGGGC 2640
AATTCACGTC CTTTCTCTCC TGGGTTGGAT TTCTGGAGCT AAACTCAGGT TTGCAGGAGT 2700
TAGCATTACT TCTTCACCAT GGAAAAGAAA AACAAGGACA GGTGGTTGCA TAAAGGACCC 2760
AGTGATTAAA TCGAAAGCAC CTGTGAAAAC TCAAAGTCAA TATTTTCTTT AAAGGAAGGG 2820
AGTGTACACA ATCATGGTTG TTTAAGTTAG CTACCATAGC AGAAATGACC TGAATATCAA 2880
TGATTGGCTT CAGCTGCTCA GCACGTCCTT CGGGTCGAAA AGTTGGGCAG 2930
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