EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS078-01440 
Organism
Homo sapiens 
Tissue/cell
H2171 
Coordinate
chr1:154390430-154393030 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:154390884-154390902GGATGGGAGGAAGGCAAG+6.39
ZNF263MA0528.1chr1:154390963-154390984GGGGGAGGAGGGAGCAGGGGC+6.21
ZNF263MA0528.1chr1:154391457-154391478GGGAGAGGGGGAGAGAGAGGG+6.21
ZNF263MA0528.1chr1:154391432-154391453AGAGCAGGGAAGAGGAGAGGA+6.23
Number of super-enhancer constituents: 34             
IDCoordinateTissue/cell
SE_00437chr1:154390273-154397370Adipose_Nuclei
SE_01040chr1:154390266-154394476Adrenal_Gland
SE_06653chr1:154390374-154394420Brain_Hippocampus_Middle
SE_09117chr1:154392451-154392745Brain_Mid_Frontal_Lobe
SE_09189chr1:154388527-154398657CD14
SE_14719chr1:154390449-154393846CD4_Memory_Primary_7pool
SE_16173chr1:154390869-154392998CD4_Naive_Primary_7pool
SE_17632chr1:154390245-154394418CD4p_CD25-_CD45RAp_Naive
SE_18405chr1:154389059-154394421CD4p_CD25-_Il17-_PMAstim_Th
SE_19165chr1:154390146-154394423CD4p_CD25-_Il17p_PMAstim_Th17
SE_24531chr1:154390928-154392675Colon_Crypt_2
SE_24531chr1:154392681-154392974Colon_Crypt_2
SE_26130chr1:154390648-154394176Duodenum_Smooth_Muscle
SE_26877chr1:154390381-154397107Esophagus
SE_32086chr1:154390256-154393099Gastric
SE_36673chr1:154390756-154393680HMEC
SE_41139chr1:154390423-154394426Left_Ventricle
SE_41647chr1:154390541-154393000LNCaP
SE_42431chr1:154390433-154394432Lung
SE_43544chr1:154384840-154394484MM1S
SE_44716chr1:154390741-154394024NHDF-Ad
SE_47983chr1:154390623-154393036Pancreas
SE_48261chr1:154388323-154397557Psoas_Muscle
SE_48934chr1:154390514-154394206Right_Atrium
SE_50453chr1:154390541-154394239Sigmoid_Colon
SE_51380chr1:154389216-154394408Skeletal_Muscle
SE_52880chr1:154390698-154393024Small_Intestine
SE_54278chr1:154390562-154394244Spleen
SE_54618chr1:154390203-154397361Stomach_Smooth_Muscle
SE_59139chr1:154375857-154394038Ly3
SE_62668chr1:154357227-154415486Tonsil
SE_64458chr1:154390429-154393143NHEK
SE_65390chr1:154390491-154396964Pancreatic_islets
SE_67236chr1:154384840-154394484MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1154391539154392211
Number: 1             
IDChromosomeStartEnd
GH01I154417chr1154390221154396888
Enhancer Sequence
AAACTCCTGA CCTTGTGATC CGACCTTCTC TGTCTCCCAA AGTGCTGGGA TTACAGGCGT 60
GAGCCACTTC ACCCGGCCTA ATTTTTGTAT TTTTTGGTAT GGATGGGGTT TCACCATTTT 120
GGCTAGGCTG GTCTTGAACT CCTGATCTCA GGTGATCCGC CAGCCTCAGC CTCCCAAAGT 180
GCTGAGATTA CAGGCGTGAG CTGCCGCACA TGGCCTTAGA TATCTTTTCC TCTAATTAGT 240
TTATAATCTC TGAGAGTTGA CCCAGGTTGT ACCTTCTTGG ACTGGAGCCA GGTGGTTATC 300
TCTGATGCTG CCAGAGGAGG ATTAGATGTT TTATCTCCTG AGTTGGTCAC ACGCGCACGT 360
GGGTCTCTGA GTCAGCATTG AGCATTACCT GTTTATGGGT CCAAAGGAGC CTCCCTCCCA 420
GACCCTCTCT CCAGCAGTGT ACAGTCCATC GTGTGGATGG GAGGAAGGCA AGGCCAAGGT 480
AAATACTGAC TCAGACAAAT ACAAGCAGGT ACAAGAAGTA CAAATACATA TGTGGGGGAG 540
GAGGGAGCAG GGGCCTGCCA GCCAAAGCTA GTCATCTGAG AAGAGGGGGT TGCGGACAGG 600
TGGGGCTGGG AGCTGAGTCA GAGAAGGTTG CTGGGCCTCC CATTAGAGCC TGGGAGCCTT 660
GACTTGCCGT AGCCTGCGGC CTTGCCTCTT CCTGGACAGT GGCCGAGGGT GCCCTCTGAA 720
ATGTTAAGGA GAAATGAATG GGCCCAGATG GTGGGGTGAC TTGGGGAGGA CGCGAGATTT 780
GGAGTCCAAG GGGAGGCAGT TTTAGGCTCT AACTCATCCT ATACACGCTG CGGCTGTGGG 840
GGAAGGGAGA GAAAGGCCAA GGGCACGACT CCTGGCTCCT GAGAGTCCCC AGTGCCCCAT 900
TAGGTTGGCA GCTGCAGTGA TGGCGCTGAC CCCCCCTTGT GCACACCCCT CAAGCCTCAG 960
CATTCCCTTC CCTGGGCCTC TGAAGGGTGG AAAGATGTGA GAAGAGCAGG GAAGAGGAGA 1020
GGAAATTGGG AGAGGGGGAG AGAGAGGGTG GTGGGGAGCC CAGAGAAGGG AGCTGGGGGT 1080
GGAGCATGGA GAGGTACCTG GGCCAAGTAG AGAGAGGCTT TGGCCAGGCT CATCTGGGTC 1140
CAGCGTGGAT TCCCTCATGC ATGAGCTGTG TGAATTTGGG CAAGTTCCCT AACTTCTCTG 1200
ATCTCTTGTT GCCTCAACAA TGAAATGGGG ACAAGACTTC CTCCCTGGCA GACTTTTTGT 1260
GAGTAGTGTG CTCTTAGGGA AAGCCCAGGG CGCAGGGTAA GTGTCCCAGT TGCTAATGAT 1320
TGTTATGGTT ATTATCACAT CAAAGCCAGG AGCCAGTCTC AGTCCAAAGA TGGAGAATGC 1380
AAGAACAGGT GACCAAGAGC ACTGGGACTT GTCCTAGCCC TCGTGGGACC AAATTCTATA 1440
CTTGTTTCCA TGTGGACACA AGGTGTCCAC AGGCTTCTCC TGGAGGCTTC TCAGCACCCA 1500
CCTACTTTTA GATCAAGACC ATTATTGCTG ACAGGGGACC TTTGTTTCCT CTGTAGCCCC 1560
TTCTGAAATC CTATGCCTTT GCAACCCAAG AAGCTGGGTT AGGCTGGGGG CCTCCTGTGC 1620
TGCCAGCTGG CCTGGGCAGC GGGGACCTGC GTCTCTGCTC AGAAACTGGG GTGGTGAGAT 1680
GGGATTAGCA GGCACGAGCC AAGCCTGTGT CCTCGGTGGC AGGCCAGGCA GCTGGTTCAC 1740
CGCTTACATA AACGGGGCCA GGAAGCTGAA CTTGTTTTTG CTGGCAAGAG CTGCGGCAAG 1800
CTGCAAGAGA GTTGAGAAAT ATGTGTCTCC GTGTGCGTGT TTTTCTCTGG TTATTGACAT 1860
TTGCAAGTTT ACTTGAAGAG GGGGAAAAAG TAGAAAAACA ACAAAGCTGT TTGGATTCCT 1920
GGCACCCAAA CTTAGGTCCC AACTGGGGAG GAACCCCACT TTCCCAGAGC TGTGCTGCAG 1980
GGTCCCCAGA CCAAAGGGTG TCTGGGCCAT GGTGGGGGTC CCAGTGTCCC TGGGAGGGGG 2040
AATCCTAGGC CACCGGGGCA GGGAGATATG GGCTTGCTTG TTGGGAGTTA CTAGGACCTA 2100
AACTCTCTTT CCCTTGAGGA ATGGGAGGCA AGGGAGGTTG TGGGAATTTT CCCTCCCCTA 2160
GAGCTCTCCA GGGAGAAAGA AGCATTTTTC TGAGGGCACT GGGATGATCT GGTCATCATC 2220
CTTCTCCCAA AGCCATCAAC TATTAAATAA TAAATCCATA GATTCATTAT GTGTTTTCAA 2280
GCTGAGTATT GTTTGCTTCC TGCCCTCTGA GAGCTAATGA TTGGGCGCCA TGGGATGCTA 2340
GACCGCAGGA GTGGGGGCCT GTGGGGGATC TACAGGTCAC AGTCTGAATC CTCATTTCAC 2400
AGAGAAGGCC AGTGGGCTCT GCCAGGGGCG GTGACGTGCC CATGGCTGCC TGTGAGTCAT 2460
CACAAGACCA GGAATAGAAC TCAGGTCACC TGACAGCACA GAGCTGTTTC CTCTACACCA 2520
AGGGGCCTCC TGCTTGTGGA GATGTACTTT ATTTTATTTT ATTTATTTAT TTATTTATTT 2580
ATTTATTTTC AAGAAGGAGT 2600