| Tag | Content |
|---|
EnhancerAtlas ID | HS136-10196 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr2:28600450-28603300 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr2:28600874-28600892 | AGAGGGAGGGAAGGAGGG | + | 6.03 | | EWSR1-FLI1 | MA0149.1 | chr2:28600878-28600896 | GGAGGGAAGGAGGGAGGA | + | 6.05 | | ZEB1 | MA0103.3 | chr2:28600847-28600858 | GGGCAGGTGGG | - | 6.14 | | ZNF263 | MA0528.1 | chr2:28600540-28600561 | GGTGAAGGGAGGGGAAGAAGG | + | 6.5 | | ZNF263 | MA0528.1 | chr2:28600875-28600896 | GAGGGAGGGAAGGAGGGAGGA | + | 7.39 |
|
| | Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
| SE_02920 | chr2:28599561-28601101 | Bladder | | SE_02920 | chr2:28601345-28602276 | Bladder | | SE_09457 | chr2:28600588-28602584 | CD14 | | SE_18763 | chr2:28601601-28602332 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_20015 | chr2:28600839-28603526 | CD56 | | SE_22508 | chr2:28601257-28603053 | CD8_primiary | | SE_23078 | chr2:28598089-28602675 | Colon_Crypt_1 | | SE_23736 | chr2:28598363-28602327 | Colon_Crypt_2 | | SE_24706 | chr2:28597998-28602775 | Colon_Crypt_3 | | SE_24706 | chr2:28603010-28603467 | Colon_Crypt_3 | | SE_25842 | chr2:28599329-28605934 | Duodenum_Smooth_Muscle | | SE_26550 | chr2:28598695-28603580 | Esophagus | | SE_27724 | chr2:28599333-28602272 | Fetal_Intestine | | SE_27724 | chr2:28602809-28606862 | Fetal_Intestine | | SE_28654 | chr2:28599422-28602161 | Fetal_Intestine_Large | | SE_28654 | chr2:28602893-28606870 | Fetal_Intestine_Large | | SE_29693 | chr2:28600789-28602243 | Fetal_Muscle | | SE_31386 | chr2:28598655-28606836 | Gastric | | SE_33745 | chr2:28599607-28603153 | H2171 | | SE_34659 | chr2:28599324-28602394 | HeLa | | SE_36417 | chr2:28599847-28602208 | HMEC | | SE_48134 | chr2:28600160-28602310 | Psoas_Muscle | | SE_50076 | chr2:28598606-28603073 | Sigmoid_Colon | | SE_51112 | chr2:28600641-28602370 | Skeletal_Muscle | | SE_52349 | chr2:28598286-28606435 | Small_Intestine | | SE_53354 | chr2:28601073-28602344 | Spleen | | SE_55359 | chr2:28600287-28600833 | Thymus | | SE_55359 | chr2:28601399-28601909 | Thymus | | SE_62927 | chr2:28581266-28660518 | Tonsil | | SE_64959 | chr2:28600200-28602183 | NHEK | | SE_65553 | chr2:28601380-28602038 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 28600937 | 28601380 | | chr2 | 28601800 | 28602147 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I028376 | chr2 | 28599357 | 28606748 |
|
Enhancer Sequence | AACTCCCTGG GGCAGAAAGT GTCTCTTCTG AAAGCAAGAC AAGAGTTTAA TGAAGCCCTA 60
AACGCGCACA GTTGAGCCTG AAATTAGGGT GGTGAAGGGA GGGGAAGAAG GCAGTTGAGG 120
ACATGGGGGC TTCAGCCCAG CCCTGCCCCA GCTGAGCAAA GCAACCTGCA AGCAAACATT 180
TGCAGAGCCC GAGGGCTTGG TTACAAAACA TTTCTGACCT AGAAAGGGGA GAATGCCACG 240
TTCCCTTCCC CCCAGACTCA GGTTTGGGGA GTGGTGTTGG GGTTTGGGGT TAATTTGGAA 300
AGGGGGAACC AACAGGTAAA GAGAGGCCAC CTCTGAAGGT GGATGCCTGG GTCTCTGAGG 360
GTGTGGGGGG AAGCATGGGT CTGCCCGGAC TGAAGCTGGG CAGGTGGGAA CCCTCCCCAC 420
CCTGAGAGGG AGGGAAGGAG GGAGGACACT GAGGGCTGCT GGGCTCTAGG TAAGCCAGTC 480
AGACTGCACA CACAGGTGTG CCAGGGCTGG GACTCCTGCC CAGGACACCC AGCACCGCTC 540
TACCAGGTGG GCAAAGCTCA TTCTGCTCCC CAAAGAGGAA GGGAGTGGCC AGCCCTGAAG 600
GGAGTGGCCA GCCCTGATTG ACACAACCAG CTGGGCTCCT GGCTTTAGGG ACAAAGCAAC 660
TGAGACTTGC TTTTACCAAT GGTTGCAGGC ATCTGGACAA CTGGCAGTGT TGAAGGGAGC 720
ACTGGCCTCA GCCCCTCTCT ATCCTGTCCC CAGGTCTCCC CAAAATGCTG CTGAGACATT 780
CAAACCGCAG CCTCCTCCTT TACCTGGTAA TTGATCCTCT TTTGCCCTGC AACTTGGGTT 840
TGGTCTTAAT TTGCCAGGCA CTAAAGGCAA GAAGAGACGG GCAGGAGGGC GTGTTATCGC 900
TTGTCTCCGG GCACAGAGGC TGTTGCAACA GAGCTCCTGA GTGCGTGTAA GAGTGCACGC 960
GTGTAGCAGA GGAAGGGAAC AGGCTGCACA TGGGGTGGAG GATGGGTGCC AGCTTTCCTC 1020
CCTTGTGTGT GCCTATGGCA GGGGGAGGGT CACTGGGCTG ATTTCTGTCC CTGAGGCAGG 1080
AGACCCCAGG ACACAAAACA GACCCAGCAA GGCCTCTGTA GCTGCAGCCG GTGCCTGAGC 1140
TGCTCAGCCT CCCTGTGCTG ACTGACACTG ACTGAAGCTG GTCTCATAGC CCAACTCGTA 1200
GCTTCTCAGC CAGTCTTGAC TGGCACCTGC CTGGCAGCCC ATTGACCACT TAGTGGAGAT 1260
GGTATGACAC CCTGGGGGCT AGAAGCTGGT TGTAGGTTCT TTGACTTTAA GGGACTATCT 1320
TCTAAAGAGG CCAAAGTAGG CACCTTTGCT GGTGGCTCTG GCAGAGCTGC GGAAGCAGCA 1380
GCTCAAGTTC TGCCTTGAAG CTGAGTCCAT TTGCTTTCCC CCTTCCCGGG ACAGACGCGG 1440
AATCCTACCA CAGTTATCCC ATCACCGAAT CAAAGGTATC ATGGGGGGTG ACGACCAGTG 1500
GGCAGGGGGT CAGAAGAGGC CCTGGGATCA CTCAGTGCAG ACTCCTTCGC CGCCTTCCTC 1560
CTCAGCACCC CTACCTCTCT TGGTTTCCTG TGGCTGCTAT AACAGAGGAC CACAAACTTG 1620
GTGGTTTAAA ATAACAGACT CTTCCTCTTT CACAGTTCTG GAGGCCAGAA GTCGGAAATC 1680
AAGGTGTCGG CAGGGCCTCG CTCCCTCTGG AGGCCCTAGG GAGATCCATT CCTCATCACT 1740
TCCAGCTTCT GGAGCTGTCA GCATTCTTTA GCTTGTCCCT GCATCTGTCT CTGCTCTGTC 1800
TTTGTGAGGC CTTCTCTGTG TGCGTCATCT CCCTCTACCC CACTCTTATA AGGATACTTC 1860
CTGTTGAATT GTGGGTCTGC CCAGATAATC CAAGAATCCA AGATGATCTC CTCCTCTCAA 1920
GATTCTTAAC CTCCTTACAT CTGCAAAGAC CCTTTTTCCA AATAAGCTCA CATTCACACG 1980
TTCCCGGGAT CTGGACACAG ACCTATCTTT TTGGGAGACC ACCATTCAAC CTGCTATACC 2040
ATTCAGTGGT TGGTAGGTTG TGGCTTAGAC CCCTCTAGTG ATGGGCGGCT CACTACTGCA 2100
TGAGTTGGCT CCATCTATGT CCAAACAGGT CTAATTATTT TAAAGTTCTT ACTTGGGTGG 2160
AGCTGAAATT TTGCTCAACA GGAACTTTTA CCCACTGGCC TTAGTTCTGG TCTTCAGAGT 2220
ACATACATCT AAATAAATAA ACCCTCCAAT CCCACCACCT CTGCCCCTGA TTACAAGGCA 2280
AAAACAAAAT GAGAAAAAGG ATGAATGGGC TTAGTTTTGA TACCAGGGAA AATGCAGAGA 2340
CTCCGGTCTC CCTGGTGGCC CTGTCCCTAG GACTTTGTGC CTGTTTCCTC GCCGTAACAC 2400
CAGAGAGTGG CCGAATCACC GTTTCATGGG ATGCTTTTGA GAAATGCATC CTGGAGAGTC 2460
CCAATTTGCA CTGGTACATT AAAGGCTCTG AGAAGTCCTA AGTAAAGAAA TCCACTTAAC 2520
CCCAATATTT TCCAAACTTA TTTGAAAATA CAGTGCTTTT ATCCACTACC ATCTTCTATC 2580
ACCTTGCAAA ACTTCCTCAC TCTTTGGGGA AATGCTTTCA GTGATGCCTC GGGGTCTTTT 2640
CCAGCTTTCA CAATCTGTTT AGGTCAAACC TAATCGTTCA TGTGCTCAGA TGCCCATCCC 2700
TAGCGCTGTT GTTAAGCATT TTGCTGGAGG TAACAAATAA TCTGGAAAAT TAGAGGCCCC 2760
TGCCCCAAGC CACAGACAGC CAGGGTGAGG CTGTGGGCGA TGGCCTCCGC CTAGGGGCCC 2820
TGGGCCTCTC TAGCTCCTAC CTGGCACTAC 2850
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