EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS108-38061 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr7:130692000-130693250 
TF binding sites/motifs
Number: 11             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EHFMA0598.2chr7:130692444-130692456CACTTCCGGGTC-6.07
ELF1MA0473.2chr7:130692444-130692456CACTTCCGGGTC-6.44
ELF3MA0640.1chr7:130692443-130692456CCACTTCCGGGTC-6.12
ELF4MA0641.1chr7:130692444-130692456CACTTCCGGGTC-6.52
ELF5MA0136.2chr7:130692444-130692455CACTTCCGGGT-6.32
GabpaMA0062.2chr7:130692442-130692453GCCACTTCCGG-6.62
HNF4GMA0484.1chr7:130692555-130692570AGGGACCAAAGTTCA+6.78
ZBTB7AMA0750.2chr7:130692442-130692455GCCACTTCCGGGT-7.52
ZNF263MA0528.1chr7:130692361-130692382GAGGGAGGAAAGAAAGAAAAA+6.05
ZNF263MA0528.1chr7:130692420-130692441AGAGGAGGAGGAATTGGAAGG+6.21
ZNF263MA0528.1chr7:130692357-130692378AGAGGAGGGAGGAAAGAAAGA+7.23
Number of super-enhancer constituents: 19             
IDCoordinateTissue/cell
SE_00305chr7:130691512-130699299Adipose_Nuclei
SE_04014chr7:130691838-130693316Brain_Anterior_Caudate
SE_08450chr7:130691663-130693636Brain_Inferior_Temporal_Lobe
SE_10895chr7:130691162-130702108CD20
SE_12190chr7:130691865-130693199CD3
SE_14401chr7:130691962-130693338CD4_Memory_Primary_7pool
SE_17149chr7:130691873-130694714CD4p_CD225int_CD127p_Tmem
SE_18091chr7:130691365-130698597CD4p_CD25-_CD45ROp_Memory
SE_18806chr7:130690797-130702081CD4p_CD25-_Il17-_PMAstim_Th
SE_19100chr7:130691585-130699006CD4p_CD25-_Il17p_PMAstim_Th17
SE_22355chr7:130691842-130694348CD8_primiary
SE_25633chr7:130691882-130693298DND41
SE_25777chr7:130691568-130698289Duodenum_Smooth_Muscle
SE_32450chr7:130692075-130693187Gastric
SE_34275chr7:130690958-130702225HCT-116
SE_36057chr7:130691913-130693168HMEC
SE_59181chr7:130691702-130725831Ly3
SE_64469chr7:130691957-130694670NHEK
SE_68199chr7:130691685-130725839TC32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr7130692200130692800
Number: 1             
IDChromosomeStartEnd
GH07I131006chr7130691491130698830
Enhancer Sequence
TTACAGGTGT GAGCCACTGC ATCTGGCCTA CATTTGTATT TTAAAAAGGT AAAATTAACA 60
AAAGGTGCCC ATCTACGTAA AAAAGTCAAA AGGAACCATC TACCTGCAAG GCAGCATGAA 120
TAAAAATGTA AAGGCAAACT TAACTGTTAC AATAACATAT CAGCTCTGAG TCTAAAGGAA 180
AACGGGTGTT TGTCTAAGAA ATGTGCTAGA GAGAACCAGC CAGTTTTAAT GTGCCTTAAG 240
CAATGAAAAC CTGTTTCCTC CTTTCCTTCT TGTCCTTTTG AAAAGACAAC ATGTCACAGG 300
GAGACGTTTT TCTAACAGCA TCCATCCTGG TGACAAATGT TTGCCAAGGG TGGGGAGAGA 360
GGAGGGAGGA AAGAAAGAAA AAGAGAAGGA AGACGCCATC TGCTGACGAA AGAGAAAAGA 420
AGAGGAGGAG GAATTGGAAG GCGCCACTTC CGGGTCCGTG TCTGAGAAAT ACAACGTATC 480
ACCATAAGGC AGACTTCTAC TCAATATAAG GAAGAACTTT ATAATAATTG GAGGAATTCA 540
AAGGCAGAAT TGATCAGGGA CCAAAGTTCA AGCAGGGGGT GGCGAGGTCT CCTCAGGCAG 600
AATAATCTTT CGTAAGCTTC TCCCTCTTGA AGGAAGAACG GCCCCAGTTC AAGTAGAAGA 660
AAATACTGTG CTTATTATTT TTCTCTAATT CTTAAATGTT TCAAATAGTC TCTATCTTGA 720
TAATTCACGA TTCAAAGGAC TGAGACTGAA ACATCAAATA AGCAAGCACA CAAATTTGCC 780
TGACACCACC TGCCCCCACC CCTAGTCCCT GGGCCTTATT TCTGGGCTTG CTGCTGGGCT 840
CTCCACGGGC AGCTGGCTGC CATCGCTCCG CTGGAGGGCG GTACCATGAG CACGGATGGG 900
GCCCACATGG CAGGCAAAGC ACTGGAAATT GATGCCGCAC CCCGCTGCTG CCTCTCAGTC 960
AGCAACTGGC CAAAGCTGAT GTGTAAGTGA CCCATGTGGG CTAACACTGA GGCCTGGTCC 1020
TTACACTGGC TCCCAGAGTG TCCAGCAAAG TTAGGCTCCA ATTGTTTCCC TATCTCGCTT 1080
CCCTTAAAAT GTTTCTTTCA CCTTCCAAAC AGATAACATA CATCTCTGTC TCAGCGGAAC 1140
TCAATCCAAG AAAACACCTC ACACCATGAT GATATAAAGA TGACATAATC TACAAATCAT 1200
TGAAGATTCT CATCTTGGTT TCTTAGATTT TCTAGCCACA TATTTTAGAC 1250