EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS180-00519 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr1:16502020-16503890 
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: 32             
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_47009chr1:16503623-16504003Ovary
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
AATATATGTG AGGGGGTGGG AGGGGGTGGG ATGGGGCTCG GTGCGGGCCT GGCAGGTGTG 60
CTGGGAGGCA AGGCCTATGA CTCCTGTGGG CCTGCTCTTC CTCCCATCCC ACCCTCCACA 120
GTCCCCACCT CAGGGGCCCT GGGCCTGGGG CAGCAGGGGC CGGGATGTGT CTCTCCAGAG 180
CAGGAACGGA GGGGCCTCCG CAACTGGTTG GGGAGGGGGG GTGGATGCCA GCCCCCGCTG 240
ATTAGGTCTC AAATTAAAGC CGAGCTTGCT CCTGTCGCTG CTCAGGCAGG CCCTCCTCCT 300
GGCCACAGTT CCCTGCCTGG CCCTCTGCTT CGGGCCTCAT GGTGGCTGGT TGCTCCCAGC 360
CTAGAATTGC TAAAAGGCTC CCGTAGTGGG TAGGAGCCTC AGGGGACCTG GGAGAGGCTT 420
CAGGGGCCCT GCCTGTGCGG GGGTCTCTCC TGTGACCCTC AGACCTGAGC CAGTGTCTGG 480
GGACAAGTCA CCGTGTCAGA GGCTGCGGAG AGCAAAGCCC AGGCGGTGAT GACTTGAGTT 540
TCCAGGCCGG GTGCCAGGAG GCCCGCGGTC ACACTCCGCC TGGGGCCTGG GCTCCGGCCA 600
ACTGTCAGCA GCAGAGATTG TTGGGTTGGT TTTATTTTAA ACAAAAAAGA ACTTTGAGTG 660
GAAACATGTG TTTCTTTTTT CTCCCCCTTC CCTCTCTCCC TATCTCTCTC CATCTCATCA 720
TGGAATATTT CTCTTTTTTG TACCTCCCTT TCTCTGTTTT TCTCTCTGTC TTCCTCTATT 780
TGTCCCTGCC TCTGTCTCTC TCTCTCTCTC TCTCATTCTT TCTTTGTTTT CCTATCTCTT 840
GATTTCTCTG TCTCTTTCTC TATTTCTTTT TCCGCAGCTT TCAGGAGTCA GGAGAGGTAC 900
CAGACTTCCT CCCTCGGGGT GTGGCCTGGG CCCCTGCCAT AAAATCCCCA GGCGTGCCAC 960
GGCCCTATGT CGGGGGTCTG CCGCTCCAGG GGAGGGAGGG GGTGTCTAGC AGCGGAGGCT 1020
CCAGGACCCA AATGCTCCAT CCTCCTCCAT CCTCCTCCTC CAAGCTCCCA CTGCCCCTGC 1080
ATCTGCCCTT CCTGTGTCTG TTTTCTCTAC TAAGCATCTA GAAAATAATT CTGCAGCTTG 1140
AGACAAGTTT TAAAACACTG GTCTGGCCCA AACCACCCAT CTACAGCCAG AGACTGGCGC 1200
CGAGGAGGGG ACCATGGCCT GCTCAACACC GCACGGAGGG TTAGGGGCAA AGCCAGGCCG 1260
ACCCAGGTCC CCCACTCCCA AGTGACATTA CTGACACCCC CAAACCCACA GTCACCACAC 1320
TTCTCAGGTC CCTGCGTCTT TCAGAGGGGT GGTCTGCTTC CTAGGAAGTG ATGTGCCCTC 1380
CCCTAAGGTG GTCACCCAGC ACAAGGGTCC CCCTGGAAAA TGTCCTGCCT TGGCTGGTCA 1440
CCCCTCCCCC AGGACAGACA AGCTTTTGGG CCCCCACCTT TCAGCCCCTT CTGCCAGGCA 1500
GTAGAGAAGA GAGAAGAGAG ACTCGCAGGC ACAGTGGCTC ATGCCTGTAA TCCTAGCACT 1560
TTGGGAGGCC GAGGTGGGCA GATCACAAGG TCAGGAGATA CAGAAGAGAG ACTGGCCACC 1620
CATGCACTGG GCCCAGGTCC TAGCTCGACG TCTGAGTCCT TGTGTGACTG TGAATATGAC 1680
TTTTCCACTG GCTGGCCTCA GTTTCCCCAT CTTTGTAACA GAAGCCTTGC CTTTGCCGCG 1740
GATCCCCTCT CTGCTCTAAT ATGTTATGGT GTTCTCCTCT CCTTCCATGG AGAGGAATTC 1800
TGGAACATCA GACCAGGAGT GCCATCTCCT CTCCCAAAGT GAGAGGGACT GTCCTCAGTG 1860
TGGCCTCAAT 1870