| Tag | Content |
|---|
EnhancerAtlas ID | HS049-04780 |
Organism | Homo sapiens |
Tissue/cell | Fetal_spinal_cord |
Coordinate | chr2:219155650-219157190 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr2:219156036-219156057 | AGAGGAGGCAGGTGAGAAGGA | + | 6.49 | | ZNF263 | MA0528.1 | chr2:219156312-219156333 | AGAGGAGGGAGAGGAGATGGA | + | 7.23 |
|
| | Number of super-enhancer constituents: 34 | ID | Coordinate | Tissue/cell |
| SE_00326 | chr2:219145665-219158265 | Adipose_Nuclei | | SE_03432 | chr2:219154454-219157349 | Brain_Angular_Gyrus | | SE_06270 | chr2:219145735-219164206 | Brain_Hippocampus_Middle | | SE_08985 | chr2:219155703-219156915 | Brain_Mid_Frontal_Lobe | | SE_10092 | chr2:219146718-219159598 | CD14 | | SE_11206 | chr2:219145902-219159097 | CD20 | | SE_12180 | chr2:219148529-219157314 | CD3 | | SE_14014 | chr2:219148910-219157816 | CD34_Primary_RO01536 | | SE_15197 | chr2:219146865-219158111 | CD4_Memory_Primary_7pool | | SE_16725 | chr2:219154813-219157847 | CD4_Naive_Primary_8pool | | SE_17020 | chr2:219153033-219157989 | CD4p_CD225int_CD127p_Tmem | | SE_17694 | chr2:219145927-219158488 | CD4p_CD25-_CD45RAp_Naive | | SE_17933 | chr2:219145740-219158304 | CD4p_CD25-_CD45ROp_Memory | | SE_18906 | chr2:219145938-219158335 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19423 | chr2:219148822-219157978 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20197 | chr2:219154274-219158091 | CD56 | | SE_21204 | chr2:219148412-219158157 | CD8_Memory_7pool | | SE_22529 | chr2:219146601-219158435 | CD8_primiary | | SE_26022 | chr2:219146503-219160474 | Duodenum_Smooth_Muscle | | SE_27110 | chr2:219153196-219162475 | Esophagus | | SE_27658 | chr2:219148708-219161413 | Fetal_Intestine | | SE_28578 | chr2:219146925-219161400 | Fetal_Intestine_Large | | SE_30125 | chr2:219154218-219158006 | Fetal_Muscle | | SE_32283 | chr2:219154277-219157757 | Gastric | | SE_35648 | chr2:219153304-219159543 | HepG2 | | SE_36018 | chr2:219146032-219158345 | HMEC | | SE_45286 | chr2:219154286-219157309 | NHLF | | SE_47526 | chr2:219154386-219157655 | Pancreas | | SE_50394 | chr2:219149842-219160653 | Sigmoid_Colon | | SE_51585 | chr2:219145632-219158203 | Skeletal_Muscle | | SE_52542 | chr2:219149722-219160735 | Small_Intestine | | SE_57570 | chr2:219154969-219157318 | VACO_503 | | SE_58066 | chr2:219155603-219157310 | VACO_9m | | SE_64537 | chr2:219153043-219158397 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 219156400 | 219156743 | | chr2 | 219155683 | 219156025 |
|
Enhancer Sequence | ATGAGCTTCC ACTCTCTGGT CGTCCCAGTT CAGCCCTCTG AAAACACACA AGTATGTGTG 60
TTTCCCTTCT CTGTGGCTTC TGCTTTTTCT GAAAGGCCCA GGGTGAGGCC TGCGGTTGGA 120
GGTGCTCTGA GGTAGACAGC GTCTGGCTGA GGCACCCATT CCCAGGGGAG GAGGCTGAGC 180
CCAGGTGGCT ATTACCCCAG CTCATGACAT GAGGCTCTCC CAACACTTAC AGGATAACCC 240
ATCATTACCT CTCTGAAGGG CTCATTTTTA CAAGTGAGGC CTTGAGGTCA TAGCACAGAA 300
AGACAGGGCC CCTGACACTG TGGTCCTGCC TCTTCCATTT AAGCTATAAA CTGGTTCTCT 360
GGATCCTCAT GACTGGAGAG ACAGAGAGAG GAGGCAGGTG AGAAGGAAGT ATGGCTCCCC 420
CTTTGCGCCA ATAAAGCAGC CCCAGGAGGC ACCTGGCTCC CCTGCCACCA CTGGCCAGCC 480
CAAAGTCGCC AGCTTGGAAA CCAAAGCTCA CTAATGAGAT GAATATTTCA GAGCCCAGAG 540
AACTGGACAC CTGAGGGCCC TTCCATGACA TCTGGCTCTG ACCTGCGTTC CCAGGCCTAC 600
TTATCCCATG TCCAGGGTGC TCAGGTAGAA CCCCAAACTC CTGGGTACCA CGTAGAGGCC 660
ACAGAGGAGG GAGAGGAGAT GGAGACCCCA TAGGACAAGA ATTGGTGCCG ACCCCACAAG 720
GCCAGGGCCT GGCCTCCCAG CAGCCTCCCT CTGCTTCCTC CCACTGGTCC CTGGCTCCTG 780
CCCCAGTCTC TCCACTTGCT TTCCCTTTTC CCGTTTCTCT GTTTTGTTTT CACTCTAACC 840
CAAAGAAGTC ACGAGGAGGA TGTTACTCCC CTGTAGTTCT GTGAACCCAG CCGGGAAACA 900
GTGGCTGGAA GTGGGACTGG CAGAGGGCAA AGTCATGGTG ATAGAGGTGG CCACTTCCCC 960
ATGCCAAACA CTTGAGCTGC TCATTGGCTT CTGCCCCAGC TGCAAGCTAG GACCCCCCCT 1020
TCCCCACCCC TTAAATATTC ACCTGTCTAC ACCGAGACTG GCCTCAGCGC GTGTGGGGGC 1080
AACCTGGGGT CCGTGCCAGG CCCTGGCTGT CTCCCCTCCC TCTTCCCTCT TCTCACCAGC 1140
TGAGGGCCAT GAAAGCCCTC ATCCCACACA GCTGGCCACT CGGGCTGGCA TGGTGGATAG 1200
GCCCTGCGAC AGAGAGGCCA CTCGTGCCCG AAAGAGGGAA CACGAGGACA CCCCCAGACC 1260
CTGGCTCCGC TCACCAGTGC CCACAACACG CTGCTGGGCT CCCAAGGCTA ACCAGGTGCC 1320
ACAGACCCGG CCGCCCACCC GCGCGCCCAG GGAGAGCGAA ACGCCAAGGG CCAGGAGGGG 1380
AGATCCCCAT CTGGAACGGG CTCCTTGGGC CCAGGAGCGG GCAAGCCGGG AGCGCGCTCC 1440
GAAAAGTTTA GGCGCCCCGG CGCATGGCCG CCCCAGCCCT GGACCAGTCC CCACCGCCCA 1500
CAGTCCCCAA CGGCGCCGGC CCCGGCCCCC TGGCTTGCCT 1540
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