EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS047-18625 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr2:28599660-28602340 
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: 3             
ChromosomeStartEnd
chr22860040028601600
chr22860093728601380
chr22860180028602147
Number: 1             
IDChromosomeStartEnd
GH02I028376chr22859935728606748
Enhancer Sequence
GTGAGCAACA GGCTTTCTCT CCTACGTTAT GTCTTTCCAT TCCCCTGGAC ACCTCAGGGA 60
ACAGGTATAG TACCCTCAAT TTACGGACGG GGAGACTGAG GCTCAGAAAG ATGCAGTAAT 120
CTGCTGGAGG ACACACAGGT AGTAAGGGGC AAACCCAGGC CTCGAAGCCA GCAGGCCCTT 180
TGAGACATGC TTCTCTAGAA AGTTTCACCC CATGGAGTCC TTCCTGGGAC CAGTACAAGG 240
CAGGTCCGTC CTAGTGGTTG GGAGTGTGGT CACCACGTGC CTGCGTTGAG GGTCTGGATC 300
ACAGAGCCCA CTTTCTGGAT CCTTTTCCTC CTCTCGAGGG CCCCAGGAGG GTGGGCAAGG 360
TCTCTTGGAA TGGGGGGGCC TGGCCCCACG TGCGAGGTGA GGGCAGAGTG GGCGAGGTCC 420
CTTGGGGTGG GAGGCCTGGC CCTCCTGACG GTGAGGGCAG GGTGCGGCCA GCAGTAGTTG 480
GGAGGTGCGG GAGGCTCCTG CTCGCTGGCT GGGCAGGGTG GGGCAGGGCG GGGCAGGCAC 540
TGGGAACAGG GTGACCTGGA CACCGCGACC TGCGATCATT GAACGAGGCA CGCAGCGGTG 600
GTGGTGGAGA TAGGGAGACC CTCTGTGCCG GGGGGACCCT CACCAAGGTG GGCACCCTCT 660
GAGCCTCCCG CCCCGCTAGC TTCCCCTTGG CCACCTCTAG GCAGCTTCCA GCAAGGATGT 720
TCCTTCTCCC TCCCAACAGG CCCTCACCTG GAGCCTGCTC GGACCTGCCC TCTCCACAAA 780
GCATGGTAGC AACTCCCTGG GGCAGAAAGT GTCTCTTCTG AAAGCAAGAC AAGAGTTTAA 840
TGAAGCCCTA AACGCGCACA GTTGAGCCTG AAATTAGGGT GGTGAAGGGA GGGGAAGAAG 900
GCAGTTGAGG ACATGGGGGC TTCAGCCCAG CCCTGCCCCA GCTGAGCAAA GCAACCTGCA 960
AGCAAACATT TGCAGAGCCC GAGGGCTTGG TTACAAAACA TTTCTGACCT AGAAAGGGGA 1020
GAATGCCACG TTCCCTTCCC CCCAGACTCA GGTTTGGGGA GTGGTGTTGG GGTTTGGGGT 1080
TAATTTGGAA AGGGGGAACC AACAGGTAAA GAGAGGCCAC CTCTGAAGGT GGATGCCTGG 1140
GTCTCTGAGG GTGTGGGGGG AAGCATGGGT CTGCCCGGAC TGAAGCTGGG CAGGTGGGAA 1200
CCCTCCCCAC CCTGAGAGGG AGGGAAGGAG GGAGGACACT GAGGGCTGCT GGGCTCTAGG 1260
TAAGCCAGTC AGACTGCACA CACAGGTGTG CCAGGGCTGG GACTCCTGCC CAGGACACCC 1320
AGCACCGCTC TACCAGGTGG GCAAAGCTCA TTCTGCTCCC CAAAGAGGAA GGGAGTGGCC 1380
AGCCCTGAAG GGAGTGGCCA GCCCTGATTG ACACAACCAG CTGGGCTCCT GGCTTTAGGG 1440
ACAAAGCAAC TGAGACTTGC TTTTACCAAT GGTTGCAGGC ATCTGGACAA CTGGCAGTGT 1500
TGAAGGGAGC ACTGGCCTCA GCCCCTCTCT ATCCTGTCCC CAGGTCTCCC CAAAATGCTG 1560
CTGAGACATT CAAACCGCAG CCTCCTCCTT TACCTGGTAA TTGATCCTCT TTTGCCCTGC 1620
AACTTGGGTT TGGTCTTAAT TTGCCAGGCA CTAAAGGCAA GAAGAGACGG GCAGGAGGGC 1680
GTGTTATCGC TTGTCTCCGG GCACAGAGGC TGTTGCAACA GAGCTCCTGA GTGCGTGTAA 1740
GAGTGCACGC GTGTAGCAGA GGAAGGGAAC AGGCTGCACA TGGGGTGGAG GATGGGTGCC 1800
AGCTTTCCTC CCTTGTGTGT GCCTATGGCA GGGGGAGGGT CACTGGGCTG ATTTCTGTCC 1860
CTGAGGCAGG AGACCCCAGG ACACAAAACA GACCCAGCAA GGCCTCTGTA GCTGCAGCCG 1920
GTGCCTGAGC TGCTCAGCCT CCCTGTGCTG ACTGACACTG ACTGAAGCTG GTCTCATAGC 1980
CCAACTCGTA GCTTCTCAGC CAGTCTTGAC TGGCACCTGC CTGGCAGCCC ATTGACCACT 2040
TAGTGGAGAT GGTATGACAC CCTGGGGGCT AGAAGCTGGT TGTAGGTTCT TTGACTTTAA 2100
GGGACTATCT TCTAAAGAGG CCAAAGTAGG CACCTTTGCT GGTGGCTCTG GCAGAGCTGC 2160
GGAAGCAGCA GCTCAAGTTC TGCCTTGAAG CTGAGTCCAT TTGCTTTCCC CCTTCCCGGG 2220
ACAGACGCGG AATCCTACCA CAGTTATCCC ATCACCGAAT CAAAGGTATC ATGGGGGGTG 2280
ACGACCAGTG GGCAGGGGGT CAGAAGAGGC CCTGGGATCA CTCAGTGCAG ACTCCTTCGC 2340
CGCCTTCCTC CTCAGCACCC CTACCTCTCT TGGTTTCCTG TGGCTGCTAT AACAGAGGAC 2400
CACAAACTTG GTGGTTTAAA ATAACAGACT CTTCCTCTTT CACAGTTCTG GAGGCCAGAA 2460
GTCGGAAATC AAGGTGTCGG CAGGGCCTCG CTCCCTCTGG AGGCCCTAGG GAGATCCATT 2520
CCTCATCACT TCCAGCTTCT GGAGCTGTCA GCATTCTTTA GCTTGTCCCT GCATCTGTCT 2580
CTGCTCTGTC TTTGTGAGGC CTTCTCTGTG TGCGTCATCT CCCTCTACCC CACTCTTATA 2640
AGGATACTTC CTGTTGAATT GTGGGTCTGC CCAGATAATC 2680