EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS047-17673 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr19:44282560-44284850 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1685191chr1944283232hg19
TF binding sites/motifs
Number: 11             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr19:44283329-44283347GGAAGGAAGAAATGAGGG+6.64
EWSR1-FLI1MA0149.1chr19:44283325-44283343GGAGGGAAGGAAGAAATG+7
Foxd3MA0041.1chr19:44284389-44284401AAACAAATATTC-6.18
RREB1MA0073.1chr19:44284072-44284092TGGGTTGGGGTTGGTGGGGG-6.27
RREB1MA0073.1chr19:44284073-44284093GGGTTGGGGTTGGTGGGGGG-8.27
ZNF263MA0528.1chr19:44284533-44284554ACCCCCAGCCCCTCCTCCCTC-6.04
ZNF263MA0528.1chr19:44284606-44284627ACCCCCAGCCCCTCCTCCCTC-6.04
ZNF263MA0528.1chr19:44284791-44284812ACCCCCAGCCCCTCCTCCCTC-6.04
ZNF263MA0528.1chr19:44282865-44282886CCCCATCCCTCCTCCTCCACC-6.53
ZNF263MA0528.1chr19:44282859-44282880ACCTCTCCCCATCCCTCCTCC-7.04
ZNF263MA0528.1chr19:44282862-44282883TCTCCCCATCCCTCCTCCTCC-7.56
Number of super-enhancer constituents: 24             
IDCoordinateTissue/cell
SE_09619chr19:44280520-44286425CD14
SE_10575chr19:44280868-44284664CD19_Primary
SE_11483chr19:44280226-44290091CD20
SE_13735chr19:44278824-44286216CD34_Primary_RO01536
SE_14657chr19:44276982-44289957CD4_Memory_Primary_7pool
SE_18182chr19:44280271-44287023CD4p_CD25-_CD45ROp_Memory
SE_18680chr19:44279319-44287337CD4p_CD25-_Il17-_PMAstim_Th
SE_19217chr19:44280174-44289910CD4p_CD25-_Il17p_PMAstim_Th17
SE_20985chr19:44280759-44286788CD8_Memory_7pool
SE_23510chr19:44283153-44286285Colon_Crypt_1
SE_23897chr19:44282805-44284629Colon_Crypt_2
SE_27247chr19:44283158-44284132Esophagus
SE_31804chr19:44282607-44285946Gastric
SE_32542chr19:44280423-44286152GM12878
SE_33868chr19:44281020-44290170HCC1954
SE_34298chr19:44280305-44290264HCT-116
SE_34813chr19:44282497-44290144HeLa
SE_39921chr19:44280212-44287484K562
SE_50403chr19:44282577-44287637Sigmoid_Colon
SE_53761chr19:44282560-44285744Spleen
SE_56117chr19:44283298-44286121u87
SE_59025chr19:44248893-44290143Ly3
SE_60730chr19:44257018-44289948DHL6
SE_62525chr19:44242576-44303622Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr194428340044283793
chr194428268044282799
chr194428411444284247
chr194428284344283144
Enhancer Sequence
TTTTGTGTTT TTAGTAGAGA TGGGGTTTCA CTGTGTTAGC CAGGATGGTC TCGATGTCCT 60
GACCTTGTGA TCCGCCCACC TCGGCCTCCC AAAGTGCTGG GATTACAGGC GTGAGCCACC 120
GCGCCCGGCC CTCTATTGTC TTTTCTAACG CTGTGTGTGT ATCTCTCACT GGTGGATTTC 180
TCAGTAGCTT GATAGCCCTA TTTGTCTTTC TCTTTAGCTG TACTTCTCTA TCTTTCTGCA 240
TTTTTGTCTC CATCTCTCTT TTTCTCTCCA TGTATCTCTG TGTCTCTGTC TCTCTCTGTA 300
CCTCTCCCCA TCCCTCCTCC TCCACCCCAC CTGGTGCTTT TGGATATCTC TATCCAGTTC 360
CCTTGGACTC CCTAGGGTTT TGCACCTGCC TCTCTGCCAG CCCCTCCCCC TGGGGAGCAG 420
GTGTCTGGGT CCTTTGCAGA AATGAGCTCA TTAGATTGAG ATGGAGGTGG TGAGGGGCGG 480
TGGATGTTAT TAAGAGAGTC CTCAAAAGGG GACTGAGGAG CTGTGGCTCA GGCCTGTAAT 540
CCCAGCACTT TGAGGCAGGA GGATTGCCTG AGTCCAGGAG TTCAAGACCA GCCTAGGCAA 600
CAAAGCAAGG TCCCATCTCT ACATAAAATA AAAAGGGTGG AGGGTGACCC TTAGGGTCAT 660
GTATTTTAAC CCTCACCCCA ATTTACAGAT GGGGAAACTG AGGTTCAGAG GGTTGTAACA 720
GCTTCCCCAA GGTCCCACTG ATAGAGGCAG TGGCCTGGCC ATGGTGGAGG GAAGGAAGAA 780
ATGAGGGGTG AGAAAGCAGA GGGGTGAAGT GGGGTAGGAT GGACCCCGTC TCTTCCCATC 840
TGCCAGGGTC ACTGTGTTCC CACCTCGGCT TCTGGGTGCG GTGCTTCGGC GTGGGAGCGG 900
CGGGCAGGCC CCGGCCATGC TTCCTGTTGG CATGGACTTC GGCGGCCCCA CCCCCTCAGT 960
GCCCGCCGCC TGCCAGAGGA AGCTGCATGC CTGACCCTCC ATGTGGCTCC TGGTCACTTC 1020
AGAGCTGCCC ACCACCCCCT CCAGATCCAA GTCGGAACAT CAGACCCTCA GGAATCTACC 1080
CAATCTTCAT ATCAGTGTCC GCATCTGGCC CTACCAGCCC AGTTCCACAA CCCTTCTGCC 1140
AGAGAGGTCT CCAGCCCCTC CTTTCCTGTT GAGCAAGTCT GTTCTCCCCT CAAGCCACTT 1200
ATTCCAACCC TTGTCCTTGA TCTGCCCCAT CACTGGCCTG ACCAGGGCTG GAATGTGACG 1260
GGAGCCTGCT GAGACCTGCC CTGACCCCAC TTTCCCCTTT CTTCCCTACT CACCACTCAT 1320
CTTCGGAGTC AGCCCCTCTT CCCCAAAAGC AATCAAAACC CCCTTCTCCT TAAGACTCAG 1380
GAATCCAGGA CCCAGCCCCC TCCTCTCCTG GTACCTAGGA GTCCAGGCCA CTGTAAGCCT 1440
ACCTCTCCAC TATTTCCCTG ACTAATCAGC ATGCAGATTT GGGGAGAAAT TGAGCTTGTT 1500
AACAGTGGAG ACTGGGTTGG GGTTGGTGGG GGGAGGCAGG TCGGGGGAGA GGTTTGTTTC 1560
CCATTTCCCA TCCCCACCCC CAAGGCAGTT TTTTCTGTCC TTTGCATCTA AGGCACTGGG 1620
TAAACATTAG AGGTTAGACA AGGACCAAAG AGCTGCCGCC TACTGGAAGA ACTTTGTCTT 1680
TCCTCCACTC TCCCTTCACC AAACCTGGGG CTACCTCTCC CCTTATTGGC TCTTGGGGGG 1740
CTTGAGTGTC TGATCAGCCA CCCTCTGGCC TCCAGGGGTC CTGGACCTCT GGCCGTCTAA 1800
TGGCAACATC TTCAAAGACT GAAACACTGA AACAAATATT CCCTTCCTTT TGCAGAGAAG 1860
GACCCCAGCA ACTGTCTCCT GGGAGCACCC AGGAGTCCCA GCCAAAGCCC CTCCTCCCTC 1920
AGACCCAAGA GTCTAGGCCC CCAACCTCTC CTCCCTCAGA TCCAGGAGTC CTGACCCCCA 1980
GCCCCTCCTC CCTCAGACCC AGGAGTCCAG ACCCCAGCCC CTCCTCCCTC AGACCCAGGA 2040
GTCCTGACCC CCAGCCCCTC CTCCCTCAGA CCCAGGAGTC CAGGCCCTCA GTCCCTCCTC 2100
CCTCAGACCC AGGAGTCCAA GTCCCCAGTC CCTCCTCCCT CAGACCCAGG AGTCCTGACC 2160
CTCAGCCCCT CCTCCCTCAG ACCCAGGAGT CCTGACCCCC AGCCCCCCCT CCCTCAGACC 2220
CAAGAGTCCT GACCCCCAGC CCCTCCTCCC TCAGACCTAG GAGTCCCAGC TCCCAGCCAC 2280
CATGCCCCAC 2290