EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS048-03068 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr1:201990820-201993280 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nr2f6(var.2)MA0728.1chr1:201991522-201991537GAGGTCAGAAGTTCA+6.38
TBX21MA0690.1chr1:201992769-201992779AAGGTGTGAA+6.02
TBX2MA0688.1chr1:201992769-201992780AAGGTGTGAAT+6.02
ZNF263MA0528.1chr1:201992213-201992234CGCTCCTCCTCCTCCTCCTTC-8.44
ZNF263MA0528.1chr1:201992216-201992237TCCTCCTCCTCCTCCTTCTTC-8.69
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_23058chr1:201990827-201991297Colon_Crypt_1
SE_23058chr1:201991682-201993038Colon_Crypt_1
SE_23723chr1:201990919-201991273Colon_Crypt_2
SE_23723chr1:201991793-201992845Colon_Crypt_2
SE_24689chr1:201990748-201991252Colon_Crypt_3
SE_24689chr1:201991746-201993176Colon_Crypt_3
SE_25977chr1:201991449-201992586Duodenum_Smooth_Muscle
SE_26730chr1:201991584-201993071Esophagus
SE_27624chr1:201991445-201993333Fetal_Intestine
SE_28545chr1:201991443-201993383Fetal_Intestine_Large
SE_31432chr1:201991670-201993044Gastric
SE_33417chr1:201991427-201994657H2171
SE_33792chr1:201990657-201991281HCC1954
SE_33792chr1:201991430-201993180HCC1954
SE_34304chr1:201991505-201993289HCT-116
SE_34741chr1:201990653-201993194HeLa
SE_41626chr1:201991969-201992570LNCaP
SE_43434chr1:201990679-201991267MCF-7
SE_43434chr1:201991624-201993665MCF-7
SE_50066chr1:201991627-201993065Sigmoid_Colon
SE_52354chr1:201991432-201993050Small_Intestine
SE_56834chr1:201991684-201992300VACO_400
SE_56834chr1:201992323-201993032VACO_400
SE_57376chr1:201991848-201992311VACO_503
SE_57945chr1:201991851-201992344VACO_9m
SE_57945chr1:201992487-201992749VACO_9m
SE_65333chr1:201992691-201993394Pancreatic_islets
SE_67013chr1:201991427-201994657H2171
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1201991192201991253
Enhancer Sequence
TTTACTCCCT ACATCATAAC TACCAGTGAT TTGTAGGACA GAGCACTCAA TGTAGAACAC 60
TCTTCACTTT GCAGATGAGG AAACTGAAGC TCAGAAAAGA AAGGTAACTT GCTCAAAGTC 120
ACAAATCATG TTGAATGGAG CCTGAGCTTC ATGTTGACAG CTGACCGCTT ACTGAGTATC 180
TACTAGGTGC CAGGCAATGT GTCAAGTTAT TGCTTTACAT ACATCATTCA TTCTCTCTGT 240
GTTCATTAAC TGTCTGCTGT GTGCATGGCT CCATGCTGTG TGCAGAAGAC CCAGTAGGGA 300
AGAGGTCACC CAGGGGGAGT AGGAAGCCTA GGCTATGGCC TGGCACGGTG GCTTATACCT 360
GTAATCCCAG CACTTTGGGA GGCTGAGGCG GGTAAATCAC CTGAGGGCAG GAATTTGAGA 420
CCAGCCTGGC CAACATGGCG AAACCCCATC TCTAGTAAAA ATACAAAAAT TAGCCGGGCG 480
TGGTGGCGGG TGCCTGTAAT CCCAGCTACT TTGGAGGCTG AGGCAGGAGA ATCACTTGAA 540
CCCGAGAGGA GAAGGTTGCG GTGAGCCGAG ATCACACCAC TGCACTCCAG CCAGGCGACA 600
GAGTGAGATT CCATCTCAAA AAAAAAAAAA AAAAAAAATT CCTGGTGCAG TGGCTCAGGC 660
TTGTAATCCC AGCACTTTGG GAGGCTGAGG CGGATGAATC ATGAGGTCAG AAGTTCAAAA 720
CCAGCCTGGC CAAGATGGTG AAACCGCGTC TCTACTAAAA ATACAAAAAA ATTAGCCGGG 780
TATGGTGGCA GCTGCCTGTA ATACCAGCTA CTCGGAAGGC TGAGGCAGAT AATTGCTTGA 840
ACCTGGGAGG CAGAGGTTGC AGTGAGCTGA GATCATGCCA CTGCACTCCA GACTGGGTGG 900
CAGAGTGAGA CTCCATCTCA AAAAAAAAGA AAAGAAAAGA AAGAAAGCCT AGGCTAGAGC 960
CTAGGAAATT CCAAAGACAT CTATATAAAC CTCTCAACAA GGTAGAGGAT AAGTGCCTCA 1020
TTTCACAGAT GAGCAAACTG AGGCTTCAGA GAGGTTAAGA AAAGCTTAAG CTCTCAGAGA 1080
TAGTAGTAAG TTTAGGAAAC CGGAGCTTGA ACCCTGCCTT CTTTCTTCAA TTCCACAGCT 1140
GACTCTGCTT TGAGAGGTGC TGAGCAACAC AAATGTCTCC GCTGTATGGG TGCCTAAAAC 1200
CCCACCATTA GATGTGCAGT TTGAGGAATG CCCTATGGAT ATACAAACAT GCCTGGGGTG 1260
GAGGGTGGAT TCAATGAGCA TTGCTTTCCA GGGACCCTTG GATCCTGCAG GGTGGATGGA 1320
AAGTGAGTTT TCAGTTCTTC AGAACCTCAC AGTGGCCAAC CCTTGGGAGC ATTGCCCTCT 1380
CATTCTTATC CTACGCTCCT CCTCCTCCTC CTTCTTCTGC TACGTGCAGG GCTGGGCTGG 1440
GGCACCAGCA GCAGCAATTA GCCCAGCTCA GCCGCCCGTT ACTGGAACCT GCATGTCAAC 1500
TCTGGAGCTG ATCCAAGAAA CCACACCCAG TGTCCTGCAT GACTCAACCT CACCTGCCCC 1560
CTCCACACCT GCCAGCCTCA GTGACCCAGG CCATAGTGCC CAGGGGAAAG TCCCAGCATC 1620
CTTTGGTCAA TCCTCATCTA CTCCATGTGT TTGTAAGGCC AGCTGGGATT TAGAGTCTTT 1680
GTATCACAGG CTTGATTCCG GGCTGATTTC TAGCCAGGAG AGAATGCTCC AGGCGGAGCA 1740
AATGCTGGGG TTTGGAAAAC TAGACTCTCC ATGGCAAATG CAGACAGATG GACCTCCTCT 1800
TCACTATCAT TGCTTGAAAC ACGAACAGCT TAAGGCCATG GGAGATATTA CTTTTCATAT 1860
GTCAAATTGG CAAAGAATTA AAGAATGCCC CTGATGTCTA GAGCTGGTGA GGATGTGAAG 1920
AAACTCAAAC TTGACAAAAA CCACTCGTCA AGGTGTGAAT TGAGAGACAC TTTTTTTTCG 1980
AGATGGAGTC TTGCGCTGTC GCCCACGCTG GAGTGTAGTG GTGCAATCTC AGCTCACTGC 2040
AACCTCTGCC TTCCAGATTC AAGCAGTGCT CCTGCCTCAG CCTCCCCAGT AGCTGGGACT 2100
ACAGGCACAC CACCACGCCC GGCTAATCCG CTTGCCTTGG CCTCCCAAAG TGCTGGGATT 2160
ACAGGCATGA GCCACAGTGC CTGGCCGAGA GACATTTTCT TTCTTTTTAA TTTTTTAATG 2220
TTTATTTTTA TATATTTTTA AACTTTTTTT TTTTTTGAGA TAGGGTCTTA CTCTATCACC 2280
TAGGCTGGAG TGCAGTGGCA TGATCATGGC TCACTGTAGC CTTGAGCCTC CCCCACCCCC 2340
AGGGCCCAAG TGATCCTCCC ATCTCAGCCT CCCAAGTAGT TGGGACCGCA GTCATGTGCC 2400
ACCGCACCCA GCTAATTTTT TAATTTAATT TTATTTTTGT AGAGACAGGA GTCTCACTGT 2460