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

TagContent
EnhancerAtlas ID
HS036-00062 
Organism
Homo sapiens 
Tissue/cell
endometrioid_adenocarcinoma 
Coordinate
chr1:16501970-16503740 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
BCL6BMA0731.1chr1:16503374-16503391TGCTTCCTAGGAAGTGA+6.08
RREB1MA0073.1chr1:16502026-16502046TGTGAGGGGGTGGGAGGGGG-6.61
RREB1MA0073.1chr1:16502036-16502056TGGGAGGGGGTGGGATGGGG-7.16
SOX10MA0442.2chr1:16502839-16502850TTCTTTGTTTT-6.62
ZNF263MA0528.1chr1:16503057-16503078CATCCTCCTCCATCCTCCTCC-6.3
ZNF263MA0528.1chr1:16503060-16503081CCTCCTCCATCCTCCTCCTCC-8.07
Number of super-enhancer constituents: 31             
IDCoordinateTissue/cell
SE_23091chr1:16501962-16502745Colon_Crypt_1
SE_23091chr1:16502844-16503560Colon_Crypt_1
SE_23751chr1:16502050-16502674Colon_Crypt_2
SE_23751chr1:16502855-16503434Colon_Crypt_2
SE_24743chr1:16497841-16502803Colon_Crypt_3
SE_24743chr1:16502816-16503501Colon_Crypt_3
SE_26540chr1:16496436-16504779Esophagus
SE_28102chr1:16497879-16504574Fetal_Intestine
SE_29455chr1:16497964-16506131Fetal_Intestine_Large
SE_31527chr1:16499336-16504399Gastric
SE_34268chr1:16497740-16504248HCT-116
SE_34628chr1:16497415-16506115HeLa
SE_36144chr1:16502024-16503485HMEC
SE_38062chr1:16499064-16503878HUVEC
SE_40833chr1:16501759-16503971Left_Ventricle
SE_44998chr1:16502053-16503662NHLF
SE_46140chr1:16501795-16503844Osteoblasts
SE_47009chr1:16502010-16502676Ovary
SE_47009chr1:16502860-16503560Ovary
SE_47150chr1:16499250-16512083Panc1
SE_47539chr1:16501964-16502662Pancreas
SE_47539chr1:16502819-16503601Pancreas
SE_48744chr1:16501448-16503785Right_Atrium
SE_50427chr1:16497958-16504232Sigmoid_Colon
SE_52536chr1:16501918-16504326Small_Intestine
SE_56795chr1:16499345-16504738VACO_400
SE_57357chr1:16501943-16502709VACO_503
SE_57939chr1:16501961-16502682VACO_9m
SE_57939chr1:16502843-16503425VACO_9m
SE_64726chr1:16502266-16503212NHEK
SE_65472chr1:16501980-16503977Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr11650207416503312
Number: 1             
IDChromosomeStartEnd
GH01I016171chr11649794116511884
Enhancer Sequence
GCCTGGGTAT GTGGGGCTTA GGCCAGAACA AATCTTGGGA CTGAGTGTAA AATATATGTG 60
AGGGGGTGGG AGGGGGTGGG ATGGGGCTCG GTGCGGGCCT GGCAGGTGTG CTGGGAGGCA 120
AGGCCTATGA CTCCTGTGGG CCTGCTCTTC CTCCCATCCC ACCCTCCACA GTCCCCACCT 180
CAGGGGCCCT GGGCCTGGGG CAGCAGGGGC CGGGATGTGT CTCTCCAGAG CAGGAACGGA 240
GGGGCCTCCG CAACTGGTTG GGGAGGGGGG GTGGATGCCA GCCCCCGCTG ATTAGGTCTC 300
AAATTAAAGC CGAGCTTGCT CCTGTCGCTG CTCAGGCAGG CCCTCCTCCT GGCCACAGTT 360
CCCTGCCTGG CCCTCTGCTT CGGGCCTCAT GGTGGCTGGT TGCTCCCAGC CTAGAATTGC 420
TAAAAGGCTC CCGTAGTGGG TAGGAGCCTC AGGGGACCTG GGAGAGGCTT CAGGGGCCCT 480
GCCTGTGCGG GGGTCTCTCC TGTGACCCTC AGACCTGAGC CAGTGTCTGG GGACAAGTCA 540
CCGTGTCAGA GGCTGCGGAG AGCAAAGCCC AGGCGGTGAT GACTTGAGTT TCCAGGCCGG 600
GTGCCAGGAG GCCCGCGGTC ACACTCCGCC TGGGGCCTGG GCTCCGGCCA ACTGTCAGCA 660
GCAGAGATTG TTGGGTTGGT TTTATTTTAA ACAAAAAAGA ACTTTGAGTG GAAACATGTG 720
TTTCTTTTTT CTCCCCCTTC CCTCTCTCCC TATCTCTCTC CATCTCATCA TGGAATATTT 780
CTCTTTTTTG TACCTCCCTT TCTCTGTTTT TCTCTCTGTC TTCCTCTATT TGTCCCTGCC 840
TCTGTCTCTC TCTCTCTCTC TCTCATTCTT TCTTTGTTTT CCTATCTCTT GATTTCTCTG 900
TCTCTTTCTC TATTTCTTTT TCCGCAGCTT TCAGGAGTCA GGAGAGGTAC CAGACTTCCT 960
CCCTCGGGGT GTGGCCTGGG CCCCTGCCAT AAAATCCCCA GGCGTGCCAC GGCCCTATGT 1020
CGGGGGTCTG CCGCTCCAGG GGAGGGAGGG GGTGTCTAGC AGCGGAGGCT CCAGGACCCA 1080
AATGCTCCAT CCTCCTCCAT CCTCCTCCTC CAAGCTCCCA CTGCCCCTGC ATCTGCCCTT 1140
CCTGTGTCTG TTTTCTCTAC TAAGCATCTA GAAAATAATT CTGCAGCTTG AGACAAGTTT 1200
TAAAACACTG GTCTGGCCCA AACCACCCAT CTACAGCCAG AGACTGGCGC CGAGGAGGGG 1260
ACCATGGCCT GCTCAACACC GCACGGAGGG TTAGGGGCAA AGCCAGGCCG ACCCAGGTCC 1320
CCCACTCCCA AGTGACATTA CTGACACCCC CAAACCCACA GTCACCACAC TTCTCAGGTC 1380
CCTGCGTCTT TCAGAGGGGT GGTCTGCTTC CTAGGAAGTG ATGTGCCCTC CCCTAAGGTG 1440
GTCACCCAGC ACAAGGGTCC CCCTGGAAAA TGTCCTGCCT TGGCTGGTCA CCCCTCCCCC 1500
AGGACAGACA AGCTTTTGGG CCCCCACCTT TCAGCCCCTT CTGCCAGGCA GTAGAGAAGA 1560
GAGAAGAGAG ACTCGCAGGC ACAGTGGCTC ATGCCTGTAA TCCTAGCACT TTGGGAGGCC 1620
GAGGTGGGCA GATCACAAGG TCAGGAGATA CAGAAGAGAG ACTGGCCACC CATGCACTGG 1680
GCCCAGGTCC TAGCTCGACG TCTGAGTCCT TGTGTGACTG TGAATATGAC TTTTCCACTG 1740
GCTGGCCTCA GTTTCCCCAT CTTTGTAACA 1770