EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS127-01455 
Organism
Homo sapiens 
Tissue/cell
Macrophage 
Coordinate
chr1:111734940-111737190 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
BCL6BMA0731.1chr1:111735350-111735367TGCTTTTAAGGAATTCA+6.75
MSCMA0665.1chr1:111737042-111737052AACAGCTGTT+6.02
MSCMA0665.1chr1:111737042-111737052AACAGCTGTT-6.02
MYF6MA0667.1chr1:111737042-111737052AACAGCTGTT+6.02
MYF6MA0667.1chr1:111737042-111737052AACAGCTGTT-6.02
RELAMA0107.1chr1:111735541-111735551GGAAATTCCC-6.02
Number of super-enhancer constituents: 36             
IDCoordinateTissue/cell
SE_00548chr1:111731103-111739856Adipose_Nuclei
SE_09820chr1:111732766-111737633CD14
SE_10666chr1:111734737-111736772CD19_Primary
SE_11520chr1:111707642-111752738CD20
SE_11981chr1:111734412-111740334CD3
SE_14851chr1:111732908-111748239CD4_Memory_Primary_7pool
SE_15648chr1:111735190-111736704CD4_Memory_Primary_8pool
SE_15989chr1:111735276-111736505CD4_Naive_Primary_7pool
SE_15989chr1:111736681-111744339CD4_Naive_Primary_7pool
SE_16482chr1:111734952-111737246CD4_Naive_Primary_8pool
SE_17180chr1:111734752-111737483CD4p_CD225int_CD127p_Tmem
SE_17406chr1:111727560-111749237CD4p_CD25-_CD45RAp_Naive
SE_17935chr1:111728556-111748584CD4p_CD25-_CD45ROp_Memory
SE_18363chr1:111727276-111748673CD4p_CD25-_Il17-_PMAstim_Th
SE_19522chr1:111734154-111744848CD4p_CD25-_Il17p_PMAstim_Th17
SE_20205chr1:111734731-111748565CD56
SE_21249chr1:111734884-111744812CD8_Memory_7pool
SE_21711chr1:111735057-111739495CD8_Naive_7pool
SE_22036chr1:111733937-111748137CD8_Naive_8pool
SE_22415chr1:111732656-111748767CD8_primiary
SE_24170chr1:111734723-111735172Colon_Crypt_2
SE_24170chr1:111735373-111736163Colon_Crypt_2
SE_24170chr1:111736828-111737638Colon_Crypt_2
SE_25351chr1:111732691-111754239DND41
SE_27328chr1:111734461-111737751Esophagus
SE_30932chr1:111734917-111736739Fetal_Thymus
SE_32304chr1:111734292-111735250Gastric
SE_32304chr1:111735305-111736259Gastric
SE_32304chr1:111736753-111737709Gastric
SE_32464chr1:111734374-111749255GM12878
SE_50246chr1:111732689-111748417Sigmoid_Colon
SE_52868chr1:111732755-111744865Small_Intestine
SE_53613chr1:111731924-111739395Spleen
SE_55120chr1:111735211-111735666Thymus
SE_58401chr1:111735195-111775083Ly1
SE_62234chr1:111732684-111775273Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr1111736343111736397
chr1111735402111735659
chr1111735691111736003
Enhancer Sequence
TGGGACAGAG CACAGAGGAT GAGAGTCAGG GGGCCCCTGC ACCACCATGC TACACACCCC 60
TCATCGCCCA CCACCAACAG CAGCTAGAGC AGTGCTGCCC ATGCCCATGG GCAGAAAGGC 120
AAGTCTGGGG GCCATGCTGG TCACAGAGCT TGAACGTACA TTGCTGGGAG GGAGGGACAG 180
AAACTAGAGA GTCTGAGGCT TCACTATCAA GAAGGGCCTT GATTTGACCC TTCTTTTCCC 240
AGTTAGTCTT CTCAACTTAC TACTGGCCAA AAATAAAAGT GACTCTGAAG AGAAGAGGGA 300
AGAAGAGTTG CTTTCATTCA AGGAGATAAT TGATTGAGCC CCTAGCCTGT GCTCACAACT 360
GTGAGCATAC CTCACAGATG TGGATACCAG GAAGAGTAAG ACACTGACCC TGCTTTTAAG 420
GAATTCACAG TGTAGTTAAG AGACAAACAT GTAAACAAGC ACTGGAGGCT CAGCCGAGAG 480
GCAAAGCCTT TTTACCTCGC TATGTCTATC CACCCTCATC CCCAGCCTTT GCCCCCACAC 540
AGCCCCCTCT GGGCACACTC GAGGTTATTA AAGATTACCA GGTTGCTGCC TGAGTAGCTT 600
GGGAAATTCC CAGGTTCTAG GAACCTCTGC CCAGCAATTC CTACACGGAA AGTCCCACAA 660
AGGTGCCTCC TCAAGACTTT CCAGTGAAGC ATTTCTCGTC ACTCCTGCCC AAGTCACAAC 720
TTGGACCCTA CTCCTCTCGC CACCACATAC ACACAGTCCC ACTCTCTGTC TTTCTCTTTT 780
ATCCCCTGGC TTTCATGGCT CTTCTTTACT CCAGCCAAAT TGCCTCAAAG TCAAGGCCAA 840
TAAAAGCACA GATGCGGGAA TCCTTGTTTC AGTTCTGGGT TTCAAGCTGG CACTTCCTGA 900
ATTAGCAAAA TTGAGTCTCT GAGAGGCTAG CTGACTGGAA GTCCCCTCCC TGTCCGAGCT 960
TCAGGGAGCT GAAAAACTCA GTGTGGGAAG GAAGTGGGGA GTGGTGGGAT TTCCCTGAAG 1020
AAAGTAAACG TCTGAGAGGT GAATCCTGCC GACCTCCACT TCCCAAACAC TGATCTGAGG 1080
AGGAAAGGCA GAATCCCAGC TCTAGCCACA CAGGAATTTC TGGTTTCCAT TCAAGGCTGG 1140
GAGTGAAAGA GCTATTTCCA AAGCAAAAGA TGATGCCACT CCCTTCAAGG ATTACCTACA 1200
ACTAGTTCCT CTTTGGTTAT CACCCATTTT TACAGAATCT TCAACACAGA GACCCCACTG 1260
CTTGCCCAAG TTTCCTTTCC TCTGAAACCC ATGGCATTCA CCTGCCCCTC TGACTTCTGT 1320
TGAGTCCCTA ACATCCTTTT CTTCTTCCCT AAAAGATAAA AGCAGGGTTG TCAACCTAAA 1380
ATCACTGGTT TTCTCCCTCC CCAGATATGA ATAGAAGGTC TACCCCTACC CCTACTGTTT 1440
TATGACTTCT TTCATTCTCC ATTCTATTAC ATCTCCCCAC GTCCTTCTCA GATCTGAAGC 1500
CCCTAAAAGG TAGAGACCAT GGCACAATAG TACCCTGCTT CCACTATACA CAGGGATATA 1560
CTCAACTGTG AACTTAAGAA CAGAAGCTAG CACTCAGCAA TATGTGCTCA GCAGGGTGTT 1620
AGGTACCTAA TGTGCATTAT TTCATTTAAT CCTCACCACA ACCTTATGAG GTAATCACAA 1680
TCATTATTTC CATTTTTAAG AAGTTAACAA ACTAACTTAA TGGGAACCTC ATAGCTAAAG 1740
GTAGAAGAAC TGGATTTAAA CCTCCTAATT CTGCTGATTT CAATCCCTGT GCTTTCAACC 1800
AGTATGTAAT TCCGCATCCC CTTCAGGTGA AGGACCTTGT CCTGTTTGTA TCTTCCCAAT 1860
GCTTGGCATC TGGCAACCAG TTGACACACA ATAAATGTTT GTTGAATGAG TATCTACCTC 1920
CTGCCCTGTT CTCCACCCTC CCTCAGCCTT GCAAGGGCAG AATCATGTCT GCATCCACCC 1980
TAACTGGTCC CACCCAGGCT GTCCCAGGAA TACTTCCTGT CCTTCCCCAA GCTAAGTCAG 2040
GAGCATTCCT CAGGCCCAGG CAGCAGTCCT GTGTGGAGGA AGAGGCAGTG GGGGTGGTTC 2100
AAAACAGCTG TTTCTCTTGG TTTAAAGAAC AAGGAGCTAG AAACAGGAGG GTGGGCGCAT 2160
GGACCCTACA GCCCATTTTC CTTGGATAAC CTCCAGTCTG TTCCCTTGAA CCCAGGGATG 2220
CTGGGCAGTT CAGGTGAGCC GTCCAGGGGC 2250