EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS050-20844 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr14:69411920-69413880 
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ESR1MA0112.3chr14:69412827-69412844CAGGTCACCGTGCCCCG-6.41
ESR2MA0258.2chr14:69412828-69412843AGGTCACCGTGCCCC+7.41
Foxd3MA0041.1chr14:69411929-69411941AAACAAACAAAC-6.32
HNF4GMA0484.1chr14:69412530-69412545AAGGTCCAAAGTCCT+6.02
Klf1MA0493.1chr14:69412404-69412415GGCCACACCCA+6.62
MyogMA0500.1chr14:69412069-69412080CTGCAGCTGTT-6.02
Nkx2-5(var.2)MA0503.1chr14:69412711-69412722AGCCACTCAAG+6.62
Tcf12MA0521.1chr14:69412069-69412080CTGCAGCTGTT-6.62
ZNF263MA0528.1chr14:69412437-69412458GAAGGAGGAACAGGCAGAGAG+6.27
Number of super-enhancer constituents: 23             
IDCoordinateTissue/cell
SE_01544chr14:69411920-69417098Aorta
SE_09473chr14:69411857-69420150CD14
SE_17458chr14:69410354-69416786CD4p_CD25-_CD45RAp_Naive
SE_22077chr14:69411911-69413643CD8_Naive_8pool
SE_22077chr14:69413666-69415013CD8_Naive_8pool
SE_24115chr14:69411938-69413605Colon_Crypt_2
SE_25810chr14:69411075-69417124Duodenum_Smooth_Muscle
SE_26589chr14:69411934-69415136Esophagus
SE_28065chr14:69411629-69413701Fetal_Intestine
SE_28974chr14:69411656-69413729Fetal_Intestine_Large
SE_31722chr14:69411909-69413688Gastric
SE_36138chr14:69404230-69420474HMEC
SE_37016chr14:69402168-69421041HSMMtube
SE_42569chr14:69412546-69416585Lung
SE_45678chr14:69402257-69421189Osteoblasts
SE_48719chr14:69413196-69415134Right_Atrium
SE_50146chr14:69404175-69415137Sigmoid_Colon
SE_52189chr14:69411918-69412792Skeletal_Muscle_Myoblast
SE_52675chr14:69411335-69415129Small_Intestine
SE_53596chr14:69411943-69413699Spleen
SE_54485chr14:69401836-69420919Stomach_Smooth_Muscle
SE_64004chr14:69411904-69413077HSMM
SE_65495chr14:69411962-69413487Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr146941199069413140
Number: 1             
IDChromosomeStartEnd
GH14I068931chr146939771969420516
Enhancer Sequence
AGAAGAAGAA AACAAACAAA CAGCAAAGGC CCCAGAGAAA AGAGAGTAAG GTCTGTTCAA 60
AAAACTGAAA AAAAAAAAGT CACAGTGCAG GAGGGAAGAA GAGGGTGCCA GAGACTGGAG 120
ATCAACTAGC CACATGGGTG TTCGGGTTCC TGCAGCTGTT GTTTCTCCTG AGAGCAGTGG 180
AAGTCACCGA AGACATTTTA TTTTAGCTGA AAGAAACAAA TGGGGCTGTG GCGGGCTGAG 240
TTGGGCTGGG AGTGCCAATC AGATGCTGGT TACATAATTC CACCTGCATC TTAGAAAGAG 300
ACCTCTAAAT GCCATGGGAA GGGCAGATCA GAGATGGAAA AGAGTGGCTG AAAAGAGACC 360
AAGCACAAGA TCACGAAAAG GTCCCAGCCA GAGACAAAGG GAGCCAGTCC AGGGTGGCAG 420
TGTAGGAGAG GGAGAAGCAG GTGGATACAA GAGATACTCA GGAGAGACGG GGAGGAGGGG 480
CAGAGGCCAC ACCCAGATTT TCAGACCTGA GCCAACAGAA GGAGGAACAG GCAGAGAGGC 540
CACAGCTTTG CACCCATACT CCCTGCCTGC CCAGACACCT GGGGCAGCTC GCTGTTCACA 600
GCAGTCCCCA AAGGTCCAAA GTCCTGAGGC TGCAGATCTA ATTGAAAGGT CTGAGTGGAA 660
GAGCTTCAGA GATCAGGATG TCACTCCCAA CCCACTGCCC CAAGTGTTCT ACCAGTGTCA 720
ACCCAATCAA TCTTAACCAC CCCAGAAGGC ATCTCATTTT ACAGATGAGA AAACCGAGGC 780
CAAGAGCTCA CAGCCACTCA AGGTCACAGC GAACAGTAGA TGCAGGAGCC AGAATTCCAC 840
CCGCGGTGGC AGTCACACAC TTTCAACCAC AGGCTCAGTC AGCGTGACTC TCCCCAGGGC 900
CTGGCAGCAG GTCACCGTGC CCCGGCCACA CTCTCACAAC TGTCCGTAAC AGGGCCCCTC 960
CGCTCACAGC CCACCAGCCC ACCAGCCCAC CTCACCACCA CCAATCAAGT CACCCTCTGG 1020
GGGTGGGGCC CAGCAGAGGT TGAAATCCTC CTTAAGGGCC TCTTAAGGGT AAACTGGAAA 1080
GGATGACATA GTAAGGACCT AAAAGGGGTT TTCTCTAATG GACCAGGCCA ACTTTGAGAA 1140
GGAGGAAGCA GACAAGGCAG TGGGACCCCA GTTCCTGGCA TCATCAGCTG ACCCTGGAAA 1200
TACCTATTCC TCAACTTCCC TATCTGAACA AGGGAGCCAG CCCTGCCTGT GCTTCTAGAA 1260
AACTTCCCAG CCCAATAAAA AAGGCAGAGG AAGAGGGGAG AAGTGGCAGA AGTCCTACCC 1320
ACAGGACTTC CAGGACTCCA CCAGCAGCCC TGAGGAGGAG TCCCAGCCCC TCCCGCTGGG 1380
TCCATGCTGC CTAAGACCGC GCCTACGCTC TGACACCTGT GGATTCCCAG TGGTTCTAAG 1440
AAGCCCAAGG CCCCACATGC TCACTGGGGC CCTGGTTTTC AGAAGGCACA CCTGGGGAAG 1500
CATCCTAGTG GGGCTCAGGG CTCTGTCCCA CCATCCATCC CCCACTTAGT CTCTGCAGGT 1560
TCCCAAGGCC ATCATGGAGG CCCTCAGCCC TCACCTCCTT CCTGTCACTC CATCTCTCTC 1620
CATCCCCACC TTCACCTTTT CCATGCTTTA GTGGAATGTT TGCAGGCACA ATGGACACAC 1680
ATCACTGGGA GATCTCAGTT CTAAATCTGC TTCCACCACA AGGAGCTCAG GGCCTCAGGC 1740
CAGCCCCTTC AAGCTTCAGT CTCACCTGCA AAGTCTCCCA CTTTCCAAGG GGCCATACTT 1800
GTCTCATTCC AATGGGCCCC CGTGAAGATG GAATGACACA GCAACTGGCA GAGCAATCTG 1860
AGGGAAACGG CATTTCCCAG ACTGGCCCGA TTATAAAAAA GGTTAAAAGT AGAGACCCCT 1920
CACCCCAACA ACCACCATTC TGGTTCAGGA GTTCTGGGAT 1960