EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-02975 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr1:111735250-111737190 
Target genes
Number: 9             
NameEnsembl ID
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: 34             
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_24170chr1:111735373-111736163Colon_Crypt_2
SE_24170chr1:111736828-111737638Colon_Crypt_2
SE_25351chr1:111732691-111754239DND41
SE_27328chr1:111734461-111737751Esophagus
SE_30932chr1:111734917-111736739Fetal_Thymus
SE_32304chr1:111735305-111736259Gastric
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
CTTTCATTCA AGGAGATAAT TGATTGAGCC CCTAGCCTGT GCTCACAACT GTGAGCATAC 60
CTCACAGATG TGGATACCAG GAAGAGTAAG ACACTGACCC TGCTTTTAAG GAATTCACAG 120
TGTAGTTAAG AGACAAACAT GTAAACAAGC ACTGGAGGCT CAGCCGAGAG GCAAAGCCTT 180
TTTACCTCGC TATGTCTATC CACCCTCATC CCCAGCCTTT GCCCCCACAC AGCCCCCTCT 240
GGGCACACTC GAGGTTATTA AAGATTACCA GGTTGCTGCC TGAGTAGCTT GGGAAATTCC 300
CAGGTTCTAG GAACCTCTGC CCAGCAATTC CTACACGGAA AGTCCCACAA AGGTGCCTCC 360
TCAAGACTTT CCAGTGAAGC ATTTCTCGTC ACTCCTGCCC AAGTCACAAC TTGGACCCTA 420
CTCCTCTCGC CACCACATAC ACACAGTCCC ACTCTCTGTC TTTCTCTTTT ATCCCCTGGC 480
TTTCATGGCT CTTCTTTACT CCAGCCAAAT TGCCTCAAAG TCAAGGCCAA TAAAAGCACA 540
GATGCGGGAA TCCTTGTTTC AGTTCTGGGT TTCAAGCTGG CACTTCCTGA ATTAGCAAAA 600
TTGAGTCTCT GAGAGGCTAG CTGACTGGAA GTCCCCTCCC TGTCCGAGCT TCAGGGAGCT 660
GAAAAACTCA GTGTGGGAAG GAAGTGGGGA GTGGTGGGAT TTCCCTGAAG AAAGTAAACG 720
TCTGAGAGGT GAATCCTGCC GACCTCCACT TCCCAAACAC TGATCTGAGG AGGAAAGGCA 780
GAATCCCAGC TCTAGCCACA CAGGAATTTC TGGTTTCCAT TCAAGGCTGG GAGTGAAAGA 840
GCTATTTCCA AAGCAAAAGA TGATGCCACT CCCTTCAAGG ATTACCTACA ACTAGTTCCT 900
CTTTGGTTAT CACCCATTTT TACAGAATCT TCAACACAGA GACCCCACTG CTTGCCCAAG 960
TTTCCTTTCC TCTGAAACCC ATGGCATTCA CCTGCCCCTC TGACTTCTGT TGAGTCCCTA 1020
ACATCCTTTT CTTCTTCCCT AAAAGATAAA AGCAGGGTTG TCAACCTAAA ATCACTGGTT 1080
TTCTCCCTCC CCAGATATGA ATAGAAGGTC TACCCCTACC CCTACTGTTT TATGACTTCT 1140
TTCATTCTCC ATTCTATTAC ATCTCCCCAC GTCCTTCTCA GATCTGAAGC CCCTAAAAGG 1200
TAGAGACCAT GGCACAATAG TACCCTGCTT CCACTATACA CAGGGATATA CTCAACTGTG 1260
AACTTAAGAA CAGAAGCTAG CACTCAGCAA TATGTGCTCA GCAGGGTGTT AGGTACCTAA 1320
TGTGCATTAT TTCATTTAAT CCTCACCACA ACCTTATGAG GTAATCACAA TCATTATTTC 1380
CATTTTTAAG AAGTTAACAA ACTAACTTAA TGGGAACCTC ATAGCTAAAG GTAGAAGAAC 1440
TGGATTTAAA CCTCCTAATT CTGCTGATTT CAATCCCTGT GCTTTCAACC AGTATGTAAT 1500
TCCGCATCCC CTTCAGGTGA AGGACCTTGT CCTGTTTGTA TCTTCCCAAT GCTTGGCATC 1560
TGGCAACCAG TTGACACACA ATAAATGTTT GTTGAATGAG TATCTACCTC CTGCCCTGTT 1620
CTCCACCCTC CCTCAGCCTT GCAAGGGCAG AATCATGTCT GCATCCACCC TAACTGGTCC 1680
CACCCAGGCT GTCCCAGGAA TACTTCCTGT CCTTCCCCAA GCTAAGTCAG GAGCATTCCT 1740
CAGGCCCAGG CAGCAGTCCT GTGTGGAGGA AGAGGCAGTG GGGGTGGTTC AAAACAGCTG 1800
TTTCTCTTGG TTTAAAGAAC AAGGAGCTAG AAACAGGAGG GTGGGCGCAT GGACCCTACA 1860
GCCCATTTTC CTTGGATAAC CTCCAGTCTG TTCCCTTGAA CCCAGGGATG CTGGGCAGTT 1920
CAGGTGAGCC GTCCAGGGGC 1940