EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS145-12296 
Organism
Homo sapiens 
Tissue/cell
NHBE 
Coordinate
chr2:28600040-28601860 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr2:28600874-28600892AGAGGGAGGGAAGGAGGG+6.03
EWSR1-FLI1MA0149.1chr2:28600878-28600896GGAGGGAAGGAGGGAGGA+6.05
ZEB1MA0103.3chr2:28600847-28600858GGGCAGGTGGG-6.14
ZNF263MA0528.1chr2:28600540-28600561GGTGAAGGGAGGGGAAGAAGG+6.5
ZNF263MA0528.1chr2:28600875-28600896GAGGGAGGGAAGGAGGGAGGA+7.39
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_02920chr2:28599561-28601101Bladder
SE_02920chr2:28601345-28602276Bladder
SE_09457chr2:28600588-28602584CD14
SE_18763chr2:28601601-28602332CD4p_CD25-_Il17-_PMAstim_Th
SE_20015chr2:28600839-28603526CD56
SE_22508chr2:28601257-28603053CD8_primiary
SE_23078chr2:28598089-28602675Colon_Crypt_1
SE_23736chr2:28598363-28602327Colon_Crypt_2
SE_24706chr2:28597998-28602775Colon_Crypt_3
SE_25842chr2:28599329-28605934Duodenum_Smooth_Muscle
SE_26550chr2:28598695-28603580Esophagus
SE_27724chr2:28599333-28602272Fetal_Intestine
SE_28654chr2:28599422-28602161Fetal_Intestine_Large
SE_29693chr2:28600789-28602243Fetal_Muscle
SE_31386chr2:28598655-28606836Gastric
SE_33745chr2:28599607-28603153H2171
SE_34659chr2:28599324-28602394HeLa
SE_36417chr2:28599847-28602208HMEC
SE_48134chr2:28600160-28602310Psoas_Muscle
SE_50076chr2:28598606-28603073Sigmoid_Colon
SE_51112chr2:28600641-28602370Skeletal_Muscle
SE_52349chr2:28598286-28606435Small_Intestine
SE_53354chr2:28601073-28602344Spleen
SE_55359chr2:28600287-28600833Thymus
SE_55359chr2:28601399-28601909Thymus
SE_62927chr2:28581266-28660518Tonsil
SE_64959chr2:28600200-28602183NHEK
SE_65553chr2:28601380-28602038Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr22860040028601600
chr22860093728601380
Number: 1             
IDChromosomeStartEnd
GH02I028376chr22859935728606748
Enhancer Sequence
TGGCCCCACG TGCGAGGTGA GGGCAGAGTG GGCGAGGTCC CTTGGGGTGG GAGGCCTGGC 60
CCTCCTGACG GTGAGGGCAG GGTGCGGCCA GCAGTAGTTG GGAGGTGCGG GAGGCTCCTG 120
CTCGCTGGCT GGGCAGGGTG GGGCAGGGCG GGGCAGGCAC TGGGAACAGG GTGACCTGGA 180
CACCGCGACC TGCGATCATT GAACGAGGCA CGCAGCGGTG GTGGTGGAGA TAGGGAGACC 240
CTCTGTGCCG GGGGGACCCT CACCAAGGTG GGCACCCTCT GAGCCTCCCG CCCCGCTAGC 300
TTCCCCTTGG CCACCTCTAG GCAGCTTCCA GCAAGGATGT TCCTTCTCCC TCCCAACAGG 360
CCCTCACCTG GAGCCTGCTC GGACCTGCCC TCTCCACAAA GCATGGTAGC AACTCCCTGG 420
GGCAGAAAGT GTCTCTTCTG AAAGCAAGAC AAGAGTTTAA TGAAGCCCTA AACGCGCACA 480
GTTGAGCCTG AAATTAGGGT GGTGAAGGGA GGGGAAGAAG GCAGTTGAGG ACATGGGGGC 540
TTCAGCCCAG CCCTGCCCCA GCTGAGCAAA GCAACCTGCA AGCAAACATT TGCAGAGCCC 600
GAGGGCTTGG TTACAAAACA TTTCTGACCT AGAAAGGGGA GAATGCCACG TTCCCTTCCC 660
CCCAGACTCA GGTTTGGGGA GTGGTGTTGG GGTTTGGGGT TAATTTGGAA AGGGGGAACC 720
AACAGGTAAA GAGAGGCCAC CTCTGAAGGT GGATGCCTGG GTCTCTGAGG GTGTGGGGGG 780
AAGCATGGGT CTGCCCGGAC TGAAGCTGGG CAGGTGGGAA CCCTCCCCAC CCTGAGAGGG 840
AGGGAAGGAG GGAGGACACT GAGGGCTGCT GGGCTCTAGG TAAGCCAGTC AGACTGCACA 900
CACAGGTGTG CCAGGGCTGG GACTCCTGCC CAGGACACCC AGCACCGCTC TACCAGGTGG 960
GCAAAGCTCA TTCTGCTCCC CAAAGAGGAA GGGAGTGGCC AGCCCTGAAG GGAGTGGCCA 1020
GCCCTGATTG ACACAACCAG CTGGGCTCCT GGCTTTAGGG ACAAAGCAAC TGAGACTTGC 1080
TTTTACCAAT GGTTGCAGGC ATCTGGACAA CTGGCAGTGT TGAAGGGAGC ACTGGCCTCA 1140
GCCCCTCTCT ATCCTGTCCC CAGGTCTCCC CAAAATGCTG CTGAGACATT CAAACCGCAG 1200
CCTCCTCCTT TACCTGGTAA TTGATCCTCT TTTGCCCTGC AACTTGGGTT TGGTCTTAAT 1260
TTGCCAGGCA CTAAAGGCAA GAAGAGACGG GCAGGAGGGC GTGTTATCGC TTGTCTCCGG 1320
GCACAGAGGC TGTTGCAACA GAGCTCCTGA GTGCGTGTAA GAGTGCACGC GTGTAGCAGA 1380
GGAAGGGAAC AGGCTGCACA TGGGGTGGAG GATGGGTGCC AGCTTTCCTC CCTTGTGTGT 1440
GCCTATGGCA GGGGGAGGGT CACTGGGCTG ATTTCTGTCC CTGAGGCAGG AGACCCCAGG 1500
ACACAAAACA GACCCAGCAA GGCCTCTGTA GCTGCAGCCG GTGCCTGAGC TGCTCAGCCT 1560
CCCTGTGCTG ACTGACACTG ACTGAAGCTG GTCTCATAGC CCAACTCGTA GCTTCTCAGC 1620
CAGTCTTGAC TGGCACCTGC CTGGCAGCCC ATTGACCACT TAGTGGAGAT GGTATGACAC 1680
CCTGGGGGCT AGAAGCTGGT TGTAGGTTCT TTGACTTTAA GGGACTATCT TCTAAAGAGG 1740
CCAAAGTAGG CACCTTTGCT GGTGGCTCTG GCAGAGCTGC GGAAGCAGCA GCTCAAGTTC 1800
TGCCTTGAAG CTGAGTCCAT 1820